Guest guest Posted June 17, 2006 Report Share Posted June 17, 2006 Hi, A while back I posted that I have a very poor conversion of ADP to ATP and part of that was thought to be caused by receptor site blockage. I've recently had the translocator test done which looks at the mitochondrial membrane and translocator protein (TL)(TL is used to transport ATP and ADP across the mitochondiral membrane - I think it might be the site of ADP to ATP conversion too, but not 100% sure on this). I've just got the results back. I have high nickel and glutathione conjugates in mitochondria. Pictures showed glutathione conjugates with nickel in the mitochondria, that I have an odd appearance of the inside of the mitochondrial membrane and also few cristae in the membrane (TL sites are on the christae). I had a low normal magnesium and potassium. Calcium at the outer mitochondrial membrane was a high normal. Other mitochondrial results were normal (i.e. no organic sulphates, peptide complexes, lactic acid, keto-acids, organochlorides, PCBs, PBBs, dichlorobenzene, organophosphates, DNA/RNA). Serum liver derived glutathione-S-transferase was high - 53 (normal range 12-46) and red cell glutathione-S-transferase 157 (range 68- 167). Glutathione levels were normal at 1.94 mmmol/l . Affinity chromatography showed an enzyme band consistent with exposure to toxic metals. Atomic emission analysis showed the presence of nickel in the abnormal form of the enzyme. The high serum glutathione-S- transferase was unusual as nickel is usually detoxified by red cells and not the liver. The results mean that I have nickel poisoning and that nickel will be causing some energy problems. I've also got Lyme borreliosis, and I've heard that heavy metal problems are common with lyme. Cheers, Carol Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 17, 2006 Report Share Posted June 17, 2006 Hi, Carol. Thanks very much for posting these results. I think that this is a wonderful test, in that it can tell you specifically which toxin or toxins you are dealing with. Do you mean to say that the glutathione was found to be conjugated with the nickel, or that both nickel and glutathione conjugated with something unknown are present, or that the test is not able to tell whether the glutathione is conjugated with the nickel, but that it looks for both of them separately, and it found both of them? I can tell you for sure that the site of the conversion of ADP to ATP is not the translocator protein. The translocator protein strictly moves the ADP in and the ATP out of the mitochondria. The conversion is done by a separate enzyme, located on the inside of the mitochondrial inner membrane, and it is called ATP synthase. I gather that pictures were made of your mitochondria using an electron microscope. That's great! And they also did emission spectroscopy to nail down the nickel. That's also great. So your glutathione level is normal. But the glutathione transferase results are a little puzzling. I'm wondering if you have SNPs in one or the other your glutathione transferases. I don't think Dr. evaluates that, although his affinity chromatography can probably identify irregularities in the structure of the glutathione transferases. If you should happen to get a Genovations Detoxi-Genomic profile, that would nail down whether or not there are SNPs in the glutathione transferase enzymes. I may have asked you this before, and if so, please forgive me (yes, I get a little brain fog myself, probably from old age!), but do you know how you might have been particularly exposed to nickel? I recall your comments about sensitivity to your earrings, and jewelry often does contain nickel, but would you have had much exposure from jewelry? How about cooking utensils? Some stainless steels contain nickel, such as the 300 series stainless steel alloys, which are used for cooking utensils, I think, but their corrosion rates should be pretty low. Did you live downwind of any mining or metal refining works? Did you have any work-related exposure that you know of? I'm wondering whether you have had a particularly large exposure to nickel, or whether there is a genetic issue in your detox system that makes it less able to take out normal exposures to nickel. Rich > > Hi, > > A while back I posted that I have a very poor conversion of ADP to > ATP and part of that was thought to be caused by receptor site > blockage. > > I've recently had the translocator test done which looks at the > mitochondrial membrane and translocator protein (TL)(TL is used to > transport ATP and ADP across the mitochondiral membrane - I think it > might be the site of ADP to ATP conversion too, but not 100% sure on > this). I've just got the results back. > > I have high nickel and glutathione conjugates in mitochondria. > > Pictures showed glutathione conjugates with nickel in the > mitochondria, that I have an odd appearance of the inside of the > mitochondrial membrane and also few cristae in the membrane (TL > sites are on the christae). I had a low normal magnesium and > potassium. Calcium at the outer mitochondrial membrane was a high > normal. Other mitochondrial results were normal (i.e. no organic > sulphates, peptide complexes, lactic acid, keto-acids, > organochlorides, PCBs, PBBs, dichlorobenzene, organophosphates, > DNA/RNA). > > Serum liver derived glutathione-S-transferase was high - 53 (normal > range 12-46) and red cell glutathione-S-transferase 157 (range 68- > 167). Glutathione levels were normal at 1.94 mmmol/l . Affinity > chromatography showed an enzyme band consistent with exposure to > toxic metals. Atomic emission analysis showed the presence of nickel > in the abnormal form of the enzyme. The high serum glutathione-S- > transferase was unusual as nickel is usually detoxified by red cells > and not the liver. > > The results mean that I have nickel poisoning and that nickel will > be causing some energy problems. I've also got Lyme borreliosis, > and I've heard that heavy metal problems are common with lyme. > > Cheers, > Carol > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 17, 2006 Report Share Posted June 17, 2006 Hi Carol, Thanks for sharing your test results. They are very interesting. Now that you have this information, what kind of program will you follow to improve your health? carolwxyz99 wrote: >A while back I posted that I have a very poor conversion of ADP to > ATP and part of that was thought to be caused by receptor site > blockage. > > I've recently had the translocator test done which looks at the > mitochondrial membrane and translocator protein (TL)(TL is used to > transport ATP and ADP across the mitochondiral membrane - I think it might be the site of ADP to ATP conversion too, but not 100% sure on this). I've just got the results back. > > I have high nickel and glutathione conjugates in mitochondria. > > Pictures showed glutathione conjugates with nickel in the > mitochondria, that I have an odd appearance of the inside of the > mitochondrial membrane and also few cristae in the membrane (TL > sites are on the christae). I had a low normal magnesium and > potassium. Calcium at the outer mitochondrial membrane was a high > normal. Other mitochondrial results were normal (i.e. no organic > sulphates, peptide complexes, lactic acid, keto-acids, > organochlorides, PCBs, PBBs, dichlorobenzene, organophosphates, > DNA/RNA). > > Serum liver derived glutathione-S-transferase was high - 53 (normal > range 12-46) and red cell glutathione-S-transferase 157 (range 68- > 167). Glutathione levels were normal at 1.94 mmmol/l . Affinity > chromatography showed an enzyme band consistent with exposure to > toxic metals. Atomic emission analysis showed the presence of nickel in the abnormal form of the enzyme. The high serum glutathione-S-transferase was unusual as nickel is usually detoxified by red cells and not the liver. > > The results mean that I have nickel poisoning and that nickel will > be causing some energy problems. I've also got Lyme borreliosis, > and I've heard that heavy metal problems are common with lyme. > > Cheers, > Carol > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 18, 2006 Report Share Posted June 18, 2006 Hi , I will be continuing to do FIR saunas as Dr M has suggested for a while and get my DNA adducts retested. I am already taking a few things to help heavy metals as I have recently had my amalgams out, but they are only very mild. I'm taking Humet R, platinum plus (free form amino acids) and lipoceutical glutathione. I may need to add in something to mop up more heavy metals but don't know what yet. Cheers, Carol > >A while back I posted that I have a very poor conversion of ADP to > > ATP and part of that was thought to be caused by receptor site > > blockage. > > > > I've recently had the translocator test done which looks at the > > mitochondrial membrane and translocator protein (TL)(TL is used to > > transport ATP and ADP across the mitochondiral membrane - I think > it might be the site of ADP to ATP conversion too, but not 100% sure > on this). I've just got the results back. > > > > I have high nickel and glutathione conjugates in mitochondria. > > > > Pictures showed glutathione conjugates with nickel in the > > mitochondria, that I have an odd appearance of the inside of the > > mitochondrial membrane and also few cristae in the membrane (TL > > sites are on the christae). I had a low normal magnesium and > > potassium. Calcium at the outer mitochondrial membrane was a high > > normal. Other mitochondrial results were normal (i.e. no organic > > sulphates, peptide complexes, lactic acid, keto-acids, > > organochlorides, PCBs, PBBs, dichlorobenzene, organophosphates, > > DNA/RNA). > > > > Serum liver derived glutathione-S-transferase was high - 53 (normal > > range 12-46) and red cell glutathione-S-transferase 157 (range 68- > > 167). Glutathione levels were normal at 1.94 mmmol/l . Affinity > > chromatography showed an enzyme band consistent with exposure to > > toxic metals. Atomic emission analysis showed the presence of > nickel in the abnormal form of the enzyme. The high serum > glutathione-S-transferase was unusual as nickel is usually > detoxified by red cells and not the liver. > > > > The results mean that I have nickel poisoning and that nickel will > > be causing some energy problems. I've also got Lyme borreliosis, > > and I've heard that heavy metal problems are common with lyme. > > > > Cheers, > > Carol > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 18, 2006 Report Share Posted June 18, 2006 Hi Rich, Thanks for the reply. Please can you tell me what SNPs are? The test sheet showed glutathione and nickel separately. However, the notes alongside the picture said " glutathione conjugates with nickel " , and in the biochemist's notes at the bottom it said " there are significant changes to the inner mitochondrial membrane AND nickel-related glutathione conjugates are present IN the mitochondria " . The test used an " epifluorescence " microscope showing images several orders of magnitude better than that of a conventional light microscope. I've no idea how I've ended up with som much nickel in me. Nothing obvious. I started to get very sensitive to many of my earrings soon after getting the classic symptoms of Lyme borreliosis in 1991, when my ME/CFS started. I do use stainless steel saucepans and often burn them, I wonder if they can release more nickel if burnt. I'll start using glass saucepans I think. I would guess that it is something about me that can't detox nickel properly. Another potential source would be my amalgam fillings, however my dentist told me that nickel has not been put in fillings for a long time and he didn't think I could have any nickel in mine. I am going to reclarify this with him as I had some very old fillings about 25 years old that were leaking recently (a splint I was wearing went black in parts from leakage of the fillings). I've recently had my amalgams removed. I have also had thyroid problems, low TSH and lowish T4/T3 and goitre - I believe heavy metals can suppress both TSH and T4/T3 at the same time. I also have nickel DNA adducts. The biochemist believes these may have been formed by an allergy to glutathione conjugates to nickel - my system was kicking off the nickel from the glutathione which was then attaching to DNA. One very interesting thing - the biochemist studied my glutathione-S- transferase in detail around 7 years ago. Affinity chromatography of the serum liver derived enzyme showed evidence of tissue breakdown (estrogenic tissue) and not nickel or heavy metals. The red blood cell enzyme was normal - no nickel etc. This raises lots of questions - have I been exposed to lots of nickel or not detoxing it properly since 7 years ago? - or did I have lots of nickel a while back but it was not being conjugated at the time of the test, but for some reason it is being conjugated now? My health is slightly better now than 7 years ago. I have been doing FIR saunaing twice a week since January and so I suppose I could be mobilising nickel. I had my amalgams removed last autumn and have been taking platinum plus (free form amino acids with a small bit of MSM), lipoceutical glutathione and Humet R (minerals with humic and fulvic acid) so maybe these things are boosting the gluathione transferase. I'm trying to think of anything that could have given me nickel poisoning during the last 7 years. I have changed stainless steel pans and my amalgams started leaking. I had stopped wearing jewellery many years ago but now wear a supposedly copper bracelet with magnets in it. My diet has been similar - I removed junk foods many years ago, but some supplements have changed. Another interesting thing that has happened to me is that after I started borrelia treatments (with herbs - including Samento) I started getting more breast cysts and the fluid inside them was black with a dark green tinge). I had had breast cysts before but the fluid was a brown colour. I am now not herxing as badly and can cope with much higher doses of antiborrelial herbs (Samento plus chinese herbs), and the fluid in the most recent cyst 2 or 3 months ago was not black but was brown again. I wrote to the biochemist a while back and asked him what could cause the black/green colour and he said bacterial infection or nickel were the only things he knew of. I would guess it was the nickel as I haven't heard of borrelia causing black fluid - which could indicate that herxing from borrelia treatment was possibly affecting nickel detox in some way. Nickel can be estrogenic, by the way, so could easily end up in breast tissue. Would you know if glutathione-S-transferase is used to detox borrelia toxins? I was not herxing at the time of the translocator test so not stressing the system so much. Do you know if there is a link between heavy metal poisoning and Lyme? I know some LLMDs say they find heavy metal poisoning quite often in Lymies. If ADP is not converted to ATP on the TL protein, would you have any idea how blockage of the " active TL site " could reduce ADP to ATP conversion. Cheers, Carol -- In , " rvankonynen " <richvank@...> wrote: > > Hi, Carol. > > Thanks very much for posting these results. I think that this is a > wonderful test, in that it can tell you specifically which toxin or > toxins you are dealing with. > > Do you mean to say that the glutathione was found to be conjugated > with the nickel, or that both nickel and glutathione conjugated with > something unknown are present, or that the test is not able to tell > whether the glutathione is conjugated with the nickel, but that it > looks for both of them separately, and it found both of them? > > I can tell you for sure that the site of the conversion of ADP to > ATP is not the translocator protein. The translocator protein > strictly moves the ADP in and the ATP out of the mitochondria. The > conversion is done by a separate enzyme, located on the inside of > the mitochondrial inner membrane, and it is called ATP synthase. > > I gather that pictures were made of your mitochondria using an > electron microscope. That's great! And they also did emission > spectroscopy to nail down the nickel. That's also great. > > So your glutathione level is normal. But the glutathione > transferase results are a little puzzling. I'm wondering if you > have SNPs in one or the other your glutathione transferases. I > don't think Dr. evaluates that, although his affinity > chromatography can probably identify irregularities in the structure > of the glutathione transferases. If you should happen to get a > Genovations Detoxi-Genomic profile, that would nail down whether or > not there are SNPs in the glutathione transferase enzymes. > > I may have asked you this before, and if so, please forgive me (yes, > I get a little brain fog myself, probably from old age!), but do you > know how you might have been particularly exposed to nickel? I > recall your comments about sensitivity to your earrings, and jewelry > often does contain nickel, but would you have had much exposure from > jewelry? How about cooking utensils? Some stainless steels contain > nickel, such as the 300 series stainless steel alloys, which are > used for cooking utensils, I think, but their corrosion rates should > be pretty low. Did you live downwind of any mining or metal > refining works? Did you have any work-related exposure that you > know of? > > I'm wondering whether you have had a particularly large exposure to > nickel, or whether there is a genetic issue in your detox system > that makes it less able to take out normal exposures to nickel. > > Rich > > > > > > Hi, > > > > A while back I posted that I have a very poor conversion of ADP to > > ATP and part of that was thought to be caused by receptor site > > blockage. > > > > I've recently had the translocator test done which looks at the > > mitochondrial membrane and translocator protein (TL)(TL is used to > > transport ATP and ADP across the mitochondiral membrane - I think > it > > might be the site of ADP to ATP conversion too, but not 100% sure > on > > this). I've just got the results back. > > > > I have high nickel and glutathione conjugates in mitochondria. > > > > Pictures showed glutathione conjugates with nickel in the > > mitochondria, that I have an odd appearance of the inside of the > > mitochondrial membrane and also few cristae in the membrane (TL > > sites are on the christae). I had a low normal magnesium and > > potassium. Calcium at the outer mitochondrial membrane was a high > > normal. Other mitochondrial results were normal (i.e. no organic > > sulphates, peptide complexes, lactic acid, keto-acids, > > organochlorides, PCBs, PBBs, dichlorobenzene, organophosphates, > > DNA/RNA). > > > > Serum liver derived glutathione-S-transferase was high - 53 (normal > > range 12-46) and red cell glutathione-S-transferase 157 (range 68- > > 167). Glutathione levels were normal at 1.94 mmmol/l . Affinity > > chromatography showed an enzyme band consistent with exposure to > > toxic metals. Atomic emission analysis showed the presence of > nickel > > in the abnormal form of the enzyme. The high serum glutathione-S- > > transferase was unusual as nickel is usually detoxified by red > cells > > and not the liver. > > > > The results mean that I have nickel poisoning and that nickel will > > be causing some energy problems. I've also got Lyme borreliosis, > > and I've heard that heavy metal problems are common with lyme. > > > > Cheers, > > Carol > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 18, 2006 Report Share Posted June 18, 2006 Hi, Carol. > > Hi Rich, > > Thanks for the reply. Please can you tell me what SNPs are? ***SNP stands for " single nucleotide polymorphism. " ***The story goes like this: In the nucleus of each human cell (except red blood cells and a small number of other types, which don't have nuclei) there are DNA molecules that represent about 35,000 genes. Genes incorporate the code that tells the cell how to make the various enzymes and other proteins it needs. The code for one enzyme in the DNA is made up of a specific series of nucleotides in a long chain (actually there are two complementary chains in the double-helix structure of the DNA molecule, which have the same information coded into each of them). There are four different types of nucleotides, and the sequence in which they are present in a the DNA molecule is what tells the cell what the sequence of amino acids should be in the enzyme that is coded for. ***When we started with Adam and Eve, there were presumably no mistakes in the coded sequence of nucleotides. (I realize that everyone doesn't look at it that way, so if macroevolution is your favorite theory, that's fine.) In any case, down through the years, there have been mutations or changes that have occurred in the germ line of humans. The germ line includes the sperm and ova cells that eventually became new people down through the years. There are several classes of changes, but one of the main classes is the SNPs, in which only one nucleotide has been changed, which may change one amino acid in the resulting enzyme, such as one of the glutathione transferase enzymes. (I might mention that SNPs are being interpreted a little more broadly than that, and can include things like deletions of nucleotides altogether.) It is now estimated that there are over 10 million possible SNPs in the entire human genome of about 35,000 genes. We all have a bunch of them, inherited from our ancestors. The only question is which ones we have. And of course, the next question is " so what? " Lots of them don't have any effect. Some are important enough to prevent a person from being born alive in the first place. Others produce significant birth defects, and some only show up if they are " provoked " by something that goes on in a person's life, such as a toxin exposure or exposure to some disease. ***The reason I brought up SNPs in connection with your glutathione transferase enzymes is that there must be a reason why you developed nickel toxicity. One possibility is that you had a big exposure. Another possibility is that your detox system has genetic issues that cause it to work less efficiently than normal. You've established that you have enough glutathione. The next question is whether your body can use it efficiently to take out toxins, such as nickel. (Incidentally, I'm not sure whether glutathione conjugation is the only route for detoxing nickel.) That may depend on whether you have SNPs in your glutathione transferase enzymes that interfere with their normal efficient operation. Just slowing them down some might be enough to allow the nickel to build up. > > The test sheet showed glutathione and nickel separately. However, > the notes alongside the picture said " glutathione conjugates with > nickel " , and in the biochemist's notes at the bottom it said " there > are significant changes to the inner mitochondrial membrane AND > nickel-related glutathione conjugates are present IN the > mitochondria " . ***O.K., so they are hooked together. > > The test used an " epifluorescence " microscope showing images several > orders of magnitude better than that of a conventional light > microscope. ***Oh, O.K. I was pretty sure an ordinary light microscope would not be able to resolve the detail of the mitochondria. > > I've no idea how I've ended up with so much nickel in me. Nothing > obvious. I started to get very sensitive to many of my earrings > soon after getting the classic symptoms of Lyme borreliosis in 1991, > when my ME/CFS started. I do use stainless steel saucepans and > often burn them, I wonder if they can release more nickel if burnt. ***I think they would. That would speed up the corrosion quite a bit. If some of the corrosion products became incorporated in your food, that would give you a bigger exposure. Also to chromium and iron, which are generally beneficial. I doubt if you would eat burnt food, and no doubt you scrub the pans after they get burnt. The next time you used them, though, they would probably release some nickel and iron until the new chromium-oxide-rich protective layer formed on the surface of the metal. > I'll start using glass saucepans I think. I would guess that it is > something about me that can't detox nickel properly. ***I'm suspecting that, too. Glass is pretty inert. At least it doesn't contain nickel. Another > potential source would be my amalgam fillings, however my dentist > told me that nickel has not been put in fillings for a long time and > he didn't think I could have any nickel in mine. I am going to > reclarify this with him as I had some very old fillings about 25 > years old that were leaking recently (a splint I was wearing went > black in parts from leakage of the fillings). I've recently had my > amalgams removed. ***The old fillings do seem like a possibility. > > I have also had thyroid problems, low TSH and lowish T4/T3 and > goitre - I believe heavy metals can suppress both TSH and T4/T3 at > the same time. I also have nickel DNA adducts. The biochemist > believes these may have been formed by an allergy to glutathione > conjugates to nickel - my system was kicking off the nickel from the > glutathione which was then attaching to DNA. > > One very interesting thing - the biochemist studied my glutathione- S- > transferase in detail around 7 years ago. Affinity chromatography > of the serum liver derived enzyme showed evidence of tissue > breakdown (estrogenic tissue) and not nickel or heavy metals. The > red blood cell enzyme was normal - no nickel etc. This raises lots > of questions - have I been exposed to lots of nickel or not detoxing > it properly since 7 years ago? - or did I have lots of nickel a > while back but it was not being conjugated at the time of the test, > but for some reason it is being conjugated now? My health is > slightly better now than 7 years ago. ***I'm not sure what to make of this. > > I have been doing FIR saunaing twice a week since January and so I > suppose I could be mobilising nickel. I had my amalgams removed > last autumn and have been taking platinum plus (free form amino > acids with a small bit of MSM), lipoceutical glutathione and Humet R > (minerals with humic and fulvic acid) so maybe these things are > boosting the gluathione transferase. ***I don't know. > > I'm trying to think of anything that could have given me nickel > poisoning during the last 7 years. I have changed stainless steel > pans and my amalgams started leaking. I had stopped wearing > jewellery many years ago but now wear a supposedly copper bracelet > with magnets in it. My diet has been similar - I removed junk foods > many years ago, but some supplements have changed. > > Another interesting thing that has happened to me is that after I > started borrelia treatments (with herbs - including Samento) I > started getting more breast cysts and the fluid inside them was > black with a dark green > tinge). I had had breast cysts before but the fluid was a brown > colour. I am now not herxing as badly and can cope with much higher > doses of antiborrelial herbs (Samento plus chinese herbs), and the > fluid in the most recent cyst > 2 or 3 months ago was not black but was brown again. I wrote to the > biochemist a while back and asked him what could cause the > black/green colour and he said bacterial infection or nickel were the > only things he knew of. I would guess it was the nickel as I > haven't heard of borrelia causing black fluid - which could indicate > that herxing from borrelia treatment was possibly affecting nickel > detox in some way. Nickel can be estrogenic, by the way, so could > easily end up in breast tissue. Hmmm. Do you mean cysts that form on the surface of the skin, or are you talking about cysts inside the breasts, that have to be removed surgically? In any case, they don't sound like a lot of fun. > > Would you know if glutathione-S-transferase is used to detox > borrelia toxins? ***No, I don't. I was not herxing at the time of the translocator > test so not stressing the system so much. Do you know if there is a > link between heavy metal poisoning and Lyme? ***I do know that Borrelia depletes cysteine and glutathione, and since glutathione is necessary to detox heavy metals, it would make sense that they would build up if Borrelia infection is present. I know some LLMDs say > they find heavy metal poisoning quite often in Lymies. ***I think that would make sense, except you tested normal for glutathione. > > If ADP is not converted to ATP on the TL protein, would you have any > idea how blockage of the " active TL site " could reduce ADP to ATP > conversion. ***It may be a bottleneck effect. If the ADP and ATP cannot be transported in and out of the mitochondria, respectively, fast enough, then that would limit the rate of conversion of ADP to ATP, because there wouldn't be enough ADP present in the mitochondria at a given time to convert to ATP, even though the machinery in the mitochondria might be perfectly ready to do it. > > Cheers, > Carol > ***Cheers to you, too! ***Rich Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 19, 2006 Report Share Posted June 19, 2006 Hi, Thanks for the info. Glass saucepans definitely on the agenda. Regarding breast cysts, the cysts are inside. I have lots of very small ones. The odd one then sometimes gets bigger. They can be seen clearly by ultrasound. They insert a long needle into the larger cysts to syringe the fluid out - a quick procedure with no anaesthetic but probably not for the squeamish. The radiologist told me that they sometimes get all sorts of strange colours in the cyst fluid of patients - it makes you wonder what estrogenic environmental toxins people have got that they are not testing for. Regarding glutathione and Lyme herxing. I have not had such bad herxes now and I am able to increase the herb dosages much quicker, and although this has correlated with being on the herbs for longer, it has also correlated with me starting lipoceutical glutathione. Unfortunately, I don't know what my glutathione levels were before starting the lipoceutical glutathione. My SODase is poor too which won't be helping. Cheers, Carol > > Another interesting thing that has happened to me is that after I > > started borrelia treatments (with herbs - including Samento) I > > started getting more breast cysts and the fluid inside them was > > black with a dark green > > tinge). I had had breast cysts before but the fluid was a brown > > colour. I am now not herxing as badly and can cope with much higher > > doses of antiborrelial herbs (Samento plus chinese herbs), and the > > fluid in the most recent cyst > > 2 or 3 months ago was not black but was brown again. I wrote to the > > biochemist a while back and asked him what could cause the > > black/green colour and he said bacterial infection or nickel were > the > > only things he knew of. I would guess it was the nickel as I > > haven't heard of borrelia causing black fluid - which could > indicate > > that herxing from borrelia treatment was possibly affecting nickel > > detox in some way. Nickel can be estrogenic, by the way, so could > > easily end up in breast tissue. > > Hmmm. Do you mean cysts that form on the surface of the skin, or > are you talking about cysts inside the breasts, that have to be > removed surgically? In any case, they don't sound like a lot of fun. > > > > > Would you know if glutathione-S-transferase is used to detox > > borrelia toxins? > > ***No, I don't. > > I was not herxing at the time of the translocator > > test so not stressing the system so much. Do you know if there is > a > > link between heavy metal poisoning and Lyme? > > ***I do know that Borrelia depletes cysteine and glutathione, and > since glutathione is necessary to detox heavy metals, it would make > sense that they would build up if Borrelia infection is present. > > I know some LLMDs say > > they find heavy metal poisoning quite often in Lymies. > > ***I think that would make sense, except you tested normal for > glutathione. > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 19, 2006 Report Share Posted June 19, 2006 What is the translocator test, and what lab does it? Thanks! > > Hi, > > Thanks for the info. Glass saucepans definitely on the agenda. > > Regarding breast cysts, the cysts are inside. I have lots of very > small ones. The odd one then sometimes gets bigger. They can be > seen clearly by ultrasound. They insert a long needle into the > larger cysts to syringe the fluid out - a quick procedure with no > anaesthetic but probably not for the squeamish. The radiologist > told me that they sometimes get all sorts of strange colours in the > cyst fluid of patients - it makes you wonder what estrogenic > environmental toxins people have got that they are not testing for. > > Regarding glutathione and Lyme herxing. I have not had such bad > herxes now and I am able to increase the herb dosages much quicker, > and although this has correlated with being on the herbs for longer, > it has also correlated with me starting lipoceutical glutathione. > Unfortunately, I don't know what my glutathione levels were before > starting the lipoceutical glutathione. My SODase is poor too which > won't be helping. > > Cheers, > Carol > > > > > > Another interesting thing that has happened to me is that after I > > > started borrelia treatments (with herbs - including Samento) I > > > started getting more breast cysts and the fluid inside them was > > > black with a dark green > > > tinge). I had had breast cysts before but the fluid was a brown > > > colour. I am now not herxing as badly and can cope with much > higher > > > doses of antiborrelial herbs (Samento plus chinese herbs), and > the > > > fluid in the most recent cyst > > > 2 or 3 months ago was not black but was brown again. I wrote to > the > > > biochemist a while back and asked him what could cause the > > > black/green colour and he said bacterial infection or nickel > were > > the > > > only things he knew of. I would guess it was the nickel as I > > > haven't heard of borrelia causing black fluid - which could > > indicate > > > that herxing from borrelia treatment was possibly affecting > nickel > > > detox in some way. Nickel can be estrogenic, by the way, so could > > > easily end up in breast tissue. > > > > Hmmm. Do you mean cysts that form on the surface of the skin, or > > are you talking about cysts inside the breasts, that have to be > > removed surgically? In any case, they don't sound like a lot of > fun. > > > > > > > > Would you know if glutathione-S-transferase is used to detox > > > borrelia toxins? > > > > ***No, I don't. > > > > I was not herxing at the time of the translocator > > > test so not stressing the system so much. Do you know if there > is > > a > > > link between heavy metal poisoning and Lyme? > > > > ***I do know that Borrelia depletes cysteine and glutathione, and > > since glutathione is necessary to detox heavy metals, it would > make > > sense that they would build up if Borrelia infection is present. > > > > I know some LLMDs say > > > they find heavy metal poisoning quite often in Lymies. > > > > ***I think that would make sense, except you tested normal for > > glutathione. > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 19, 2006 Report Share Posted June 19, 2006 Hi, The translocator test is a mitochondrial test for those with a blockage to the translocator protein or mitochondrial membrane problems. Here's some more info from part of an info sheet Background. For the past few months, we have been asessing ATP related metabolism. In about 40% of patients with abnormalities there is a block or partial block at the TL sites in the mitochondrial membranes This specialised protein transports ADP from the cytoplasm into the mitochondria for re-conversion to ATP. The same protein also transports this ATP and newly made ATP from oxidative phosphorylation back into the cytoplasm. It is THE most important step in maintaining energy availability at thte cellular level. A block at this site is potentially serious and will lead to poor energy availability. Early in the energy expenditure cycle, patients with this problem will switch to anaerobic metabolism leading to lactate accumulation - acidosis. An acid environment further inhibits reliable TL function. The aim of further studies is to identify the cause of the block to the TL site. Suspects include environmental contaminants such as pesticides, other organic chemicals and toxic metals, partial detoxification products such as glutathione conjugates and organic sulphate conjugates, flame-retardent chemicals, peptide complexes (hormones or cytokines or peptides that mimic these) and nucleotides (RNA/DNA) from " invaders " such as viruses or bacteria. A number of fluorescence probes are used to explore these possibilities and to look at calcium, potassium, magnesium, zinc and pH levels aroud the mitochondrial membranes. Phase-contrast with digital image deconvolution is among several microscopic techniques we use to explore the mitochondrial membrane structure, membrane stability and to semi-quantify mitochondrial DNA. Cheers, Carol > > > > Hi, > > > > Thanks for the info. Glass saucepans definitely on the agenda. > > > > Regarding breast cysts, the cysts are inside. I have lots of very > > small ones. The odd one then sometimes gets bigger. They can be > > seen clearly by ultrasound. They insert a long needle into the > > larger cysts to syringe the fluid out - a quick procedure with no > > anaesthetic but probably not for the squeamish. The radiologist > > told me that they sometimes get all sorts of strange colours in the > > cyst fluid of patients - it makes you wonder what estrogenic > > environmental toxins people have got that they are not testing for. > > > > Regarding glutathione and Lyme herxing. I have not had such bad > > herxes now and I am able to increase the herb dosages much quicker, > > and although this has correlated with being on the herbs for > longer, > > it has also correlated with me starting lipoceutical glutathione. > > Unfortunately, I don't know what my glutathione levels were before > > starting the lipoceutical glutathione. My SODase is poor too which > > won't be helping. > > > > Cheers, > > Carol > > > > > > > > > > Another interesting thing that has happened to me is that after > I > > > > started borrelia treatments (with herbs - including Samento) I > > > > started getting more breast cysts and the fluid inside them was > > > > black with a dark green > > > > tinge). I had had breast cysts before but the fluid was a brown > > > > colour. I am now not herxing as badly and can cope with much > > higher > > > > doses of antiborrelial herbs (Samento plus chinese herbs), and > > the > > > > fluid in the most recent cyst > > > > 2 or 3 months ago was not black but was brown again. I wrote to > > the > > > > biochemist a while back and asked him what could cause the > > > > black/green colour and he said bacterial infection or nickel > > were > > > the > > > > only things he knew of. I would guess it was the nickel as I > > > > haven't heard of borrelia causing black fluid - which could > > > indicate > > > > that herxing from borrelia treatment was possibly affecting > > nickel > > > > detox in some way. Nickel can be estrogenic, by the way, so > could > > > > easily end up in breast tissue. > > > > > > Hmmm. Do you mean cysts that form on the surface of the skin, or > > > are you talking about cysts inside the breasts, that have to be > > > removed surgically? In any case, they don't sound like a lot of > > fun. > > > > > > > > > > > Would you know if glutathione-S-transferase is used to detox > > > > borrelia toxins? > > > > > > ***No, I don't. > > > > > > I was not herxing at the time of the translocator > > > > test so not stressing the system so much. Do you know if there > > is > > > a > > > > link between heavy metal poisoning and Lyme? > > > > > > ***I do know that Borrelia depletes cysteine and glutathione, and > > > since glutathione is necessary to detox heavy metals, it would > > make > > > sense that they would build up if Borrelia infection is present. > > > > > > I know some LLMDs say > > > > they find heavy metal poisoning quite often in Lymies. > > > > > > ***I think that would make sense, except you tested normal for > > > glutathione. > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 19, 2006 Report Share Posted June 19, 2006 HI RIch, Do you think the translocator test would pick up old exposures (eg. mercury from fillings that have been removed several years ago or toxins from vaccines) ? I ask because red blood cells only live 120 days so I wonder if this test only reflects recent or ongoing exposure. Re: Mitochondrial function - my translocator test results Hi, Carol. Thanks very much for posting these results. I think that this is a wonderful test, in that it can tell you specifically which toxin or toxins you are dealing with. Do you mean to say that the glutathione was found to be conjugated with the nickel, or that both nickel and glutathione conjugated with something unknown are present, or that the test is not able to tell whether the glutathione is conjugated with the nickel, but that it looks for both of them separately, and it found both of them? I can tell you for sure that the site of the conversion of ADP to ATP is not the translocator protein. The translocator protein strictly moves the ADP in and the ATP out of the mitochondria. The conversion is done by a separate enzyme, located on the inside of the mitochondrial inner membrane, and it is called ATP synthase. I gather that pictures were made of your mitochondria using an electron microscope. That's great! And they also did emission spectroscopy to nail down the nickel. That's also great. So your glutathione level is normal. But the glutathione transferase results are a little puzzling. I'm wondering if you have SNPs in one or the other your glutathione transferases. I don't think Dr. evaluates that, although his affinity chromatography can probably identify irregularities in the structure of the glutathione transferases. If you should happen to get a Genovations Detoxi-Genomic profile, that would nail down whether or not there are SNPs in the glutathione transferase enzymes. I may have asked you this before, and if so, please forgive me (yes, I get a little brain fog myself, probably from old age!), but do you know how you might have been particularly exposed to nickel? I recall your comments about sensitivity to your earrings, and jewelry often does contain nickel, but would you have had much exposure from jewelry? How about cooking utensils? Some stainless steels contain nickel, such as the 300 series stainless steel alloys, which are used for cooking utensils, I think, but their corrosion rates should be pretty low. Did you live downwind of any mining or metal refining works? Did you have any work-related exposure that you know of? I'm wondering whether you have had a particularly large exposure to nickel, or whether there is a genetic issue in your detox system that makes it less able to take out normal exposures to nickel. Rich > > Hi, > > A while back I posted that I have a very poor conversion of ADP to > ATP and part of that was thought to be caused by receptor site > blockage. > > I've recently had the translocator test done which looks at the > mitochondrial membrane and translocator protein (TL)(TL is used to > transport ATP and ADP across the mitochondiral membrane - I think it > might be the site of ADP to ATP conversion too, but not 100% sure on > this). I've just got the results back. > > I have high nickel and glutathione conjugates in mitochondria. > > Pictures showed glutathione conjugates with nickel in the > mitochondria, that I have an odd appearance of the inside of the > mitochondrial membrane and also few cristae in the membrane (TL > sites are on the christae). I had a low normal magnesium and > potassium. Calcium at the outer mitochondrial membrane was a high > normal. Other mitochondrial results were normal (i.e. no organic > sulphates, peptide complexes, lactic acid, keto-acids, > organochlorides, PCBs, PBBs, dichlorobenzene, organophosphates, > DNA/RNA). > > Serum liver derived glutathione-S-transferase was high - 53 (normal > range 12-46) and red cell glutathione-S-transferase 157 (range 68- > 167). Glutathione levels were normal at 1.94 mmmol/l . Affinity > chromatography showed an enzyme band consistent with exposure to > toxic metals. Atomic emission analysis showed the presence of nickel > in the abnormal form of the enzyme. The high serum glutathione-S- > transferase was unusual as nickel is usually detoxified by red cells > and not the liver. > > The results mean that I have nickel poisoning and that nickel will > be causing some energy problems. I've also got Lyme borreliosis, > and I've heard that heavy metal problems are common with lyme. > > Cheers, > Carol > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 19, 2006 Report Share Posted June 19, 2006 Hi Rich and CArol, Wouldn't the fact that the nickel is bound to glutathione mean it is in the process of being detoxified and so CArol's body is capable of detoxifiying it ? Re: Mitochondrial function - my translocator test results Hi, Carol. > > Hi Rich, > > Thanks for the reply. Please can you tell me what SNPs are? ***SNP stands for " single nucleotide polymorphism. " ***The story goes like this: In the nucleus of each human cell (except red blood cells and a small number of other types, which don't have nuclei) there are DNA molecules that represent about 35,000 genes. Genes incorporate the code that tells the cell how to make the various enzymes and other proteins it needs. The code for one enzyme in the DNA is made up of a specific series of nucleotides in a long chain (actually there are two complementary chains in the double-helix structure of the DNA molecule, which have the same information coded into each of them). There are four different types of nucleotides, and the sequence in which they are present in a the DNA molecule is what tells the cell what the sequence of amino acids should be in the enzyme that is coded for. ***When we started with Adam and Eve, there were presumably no mistakes in the coded sequence of nucleotides. (I realize that everyone doesn't look at it that way, so if macroevolution is your favorite theory, that's fine.) In any case, down through the years, there have been mutations or changes that have occurred in the germ line of humans. The germ line includes the sperm and ova cells that eventually became new people down through the years. There are several classes of changes, but one of the main classes is the SNPs, in which only one nucleotide has been changed, which may change one amino acid in the resulting enzyme, such as one of the glutathione transferase enzymes. (I might mention that SNPs are being interpreted a little more broadly than that, and can include things like deletions of nucleotides altogether.) It is now estimated that there are over 10 million possible SNPs in the entire human genome of about 35,000 genes. We all have a bunch of them, inherited from our ancestors. The only question is which ones we have. And of course, the next question is " so what? " Lots of them don't have any effect. Some are important enough to prevent a person from being born alive in the first place. Others produce significant birth defects, and some only show up if they are " provoked " by something that goes on in a person's life, such as a toxin exposure or exposure to some disease. ***The reason I brought up SNPs in connection with your glutathione transferase enzymes is that there must be a reason why you developed nickel toxicity. One possibility is that you had a big exposure. Another possibility is that your detox system has genetic issues that cause it to work less efficiently than normal. You've established that you have enough glutathione. The next question is whether your body can use it efficiently to take out toxins, such as nickel. (Incidentally, I'm not sure whether glutathione conjugation is the only route for detoxing nickel.) That may depend on whether you have SNPs in your glutathione transferase enzymes that interfere with their normal efficient operation. Just slowing them down some might be enough to allow the nickel to build up. > > The test sheet showed glutathione and nickel separately. However, > the notes alongside the picture said " glutathione conjugates with > nickel " , and in the biochemist's notes at the bottom it said " there > are significant changes to the inner mitochondrial membrane AND > nickel-related glutathione conjugates are present IN the > mitochondria " . ***O.K., so they are hooked together. > > The test used an " epifluorescence " microscope showing images several > orders of magnitude better than that of a conventional light > microscope. ***Oh, O.K. I was pretty sure an ordinary light microscope would not be able to resolve the detail of the mitochondria. > > I've no idea how I've ended up with so much nickel in me. Nothing > obvious. I started to get very sensitive to many of my earrings > soon after getting the classic symptoms of Lyme borreliosis in 1991, > when my ME/CFS started. I do use stainless steel saucepans and > often burn them, I wonder if they can release more nickel if burnt. ***I think they would. That would speed up the corrosion quite a bit. If some of the corrosion products became incorporated in your food, that would give you a bigger exposure. Also to chromium and iron, which are generally beneficial. I doubt if you would eat burnt food, and no doubt you scrub the pans after they get burnt. The next time you used them, though, they would probably release some nickel and iron until the new chromium-oxide-rich protective layer formed on the surface of the metal. > I'll start using glass saucepans I think. I would guess that it is > something about me that can't detox nickel properly. ***I'm suspecting that, too. Glass is pretty inert. At least it doesn't contain nickel. Another > potential source would be my amalgam fillings, however my dentist > told me that nickel has not been put in fillings for a long time and > he didn't think I could have any nickel in mine. I am going to > reclarify this with him as I had some very old fillings about 25 > years old that were leaking recently (a splint I was wearing went > black in parts from leakage of the fillings). I've recently had my > amalgams removed. ***The old fillings do seem like a possibility. > > I have also had thyroid problems, low TSH and lowish T4/T3 and > goitre - I believe heavy metals can suppress both TSH and T4/T3 at > the same time. I also have nickel DNA adducts. The biochemist > believes these may have been formed by an allergy to glutathione > conjugates to nickel - my system was kicking off the nickel from the > glutathione which was then attaching to DNA. > > One very interesting thing - the biochemist studied my glutathione- S- > transferase in detail around 7 years ago. Affinity chromatography > of the serum liver derived enzyme showed evidence of tissue > breakdown (estrogenic tissue) and not nickel or heavy metals. The > red blood cell enzyme was normal - no nickel etc. This raises lots > of questions - have I been exposed to lots of nickel or not detoxing > it properly since 7 years ago? - or did I have lots of nickel a > while back but it was not being conjugated at the time of the test, > but for some reason it is being conjugated now? My health is > slightly better now than 7 years ago. ***I'm not sure what to make of this. > > I have been doing FIR saunaing twice a week since January and so I > suppose I could be mobilising nickel. I had my amalgams removed > last autumn and have been taking platinum plus (free form amino > acids with a small bit of MSM), lipoceutical glutathione and Humet R > (minerals with humic and fulvic acid) so maybe these things are > boosting the gluathione transferase. ***I don't know. > > I'm trying to think of anything that could have given me nickel > poisoning during the last 7 years. I have changed stainless steel > pans and my amalgams started leaking. I had stopped wearing > jewellery many years ago but now wear a supposedly copper bracelet > with magnets in it. My diet has been similar - I removed junk foods > many years ago, but some supplements have changed. > > Another interesting thing that has happened to me is that after I > started borrelia treatments (with herbs - including Samento) I > started getting more breast cysts and the fluid inside them was > black with a dark green > tinge). I had had breast cysts before but the fluid was a brown > colour. I am now not herxing as badly and can cope with much higher > doses of antiborrelial herbs (Samento plus chinese herbs), and the > fluid in the most recent cyst > 2 or 3 months ago was not black but was brown again. I wrote to the > biochemist a while back and asked him what could cause the > black/green colour and he said bacterial infection or nickel were the > only things he knew of. I would guess it was the nickel as I > haven't heard of borrelia causing black fluid - which could indicate > that herxing from borrelia treatment was possibly affecting nickel > detox in some way. Nickel can be estrogenic, by the way, so could > easily end up in breast tissue. Hmmm. Do you mean cysts that form on the surface of the skin, or are you talking about cysts inside the breasts, that have to be removed surgically? In any case, they don't sound like a lot of fun. > > Would you know if glutathione-S-transferase is used to detox > borrelia toxins? ***No, I don't. I was not herxing at the time of the translocator > test so not stressing the system so much. Do you know if there is a > link between heavy metal poisoning and Lyme? ***I do know that Borrelia depletes cysteine and glutathione, and since glutathione is necessary to detox heavy metals, it would make sense that they would build up if Borrelia infection is present. I know some LLMDs say > they find heavy metal poisoning quite often in Lymies. ***I think that would make sense, except you tested normal for glutathione. > > If ADP is not converted to ATP on the TL protein, would you have any > idea how blockage of the " active TL site " could reduce ADP to ATP > conversion. ***It may be a bottleneck effect. If the ADP and ATP cannot be transported in and out of the mitochondria, respectively, fast enough, then that would limit the rate of conversion of ADP to ATP, because there wouldn't be enough ADP present in the mitochondria at a given time to convert to ATP, even though the machinery in the mitochondria might be perfectly ready to do it. > > Cheers, > Carol > ***Cheers to you, too! ***Rich Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 19, 2006 Report Share Posted June 19, 2006 Hi, . The translocator test is actually done on neutrophils, rather than red blood cells. Red blood cells do not have mitochondria. They derive their biochemical energy (ATP) from glycolysis. Neutrophils are the most abundant of the white blood cells, and they have mitochondria, so I suspect that's the reason Dr. has chosen to study them. They are the most conveniently sampled cells that have mitochondria. The life span of neutrophils is actually even less than that of red blood cells. Neutrophils last only a few days. New ones are produced in the bone marrow. It's a good question. To what degree do the mitochondria in neutrophils represent what is happening in the mitochondria of soft tissue, such as muscle? For toxins that are fairly mobile in the body or for current exposures, the test would seem to be fine. I suppose it's possible that some toxins from exposures in the past would be so well sequestered in the tissues that they would not show up in the neutrophils. You mentioned mercury, and it is known that mercury does not stay in the blood very long. I'll have to ask Dr. if he has done any correlations with mitochondria from muscle biopsies, for example. Rich > > > > Hi, > > > > A while back I posted that I have a very poor conversion of ADP to > > ATP and part of that was thought to be caused by receptor site > > blockage. > > > > I've recently had the translocator test done which looks at the > > mitochondrial membrane and translocator protein (TL)(TL is used to > > transport ATP and ADP across the mitochondiral membrane - I think > it > > might be the site of ADP to ATP conversion too, but not 100% sure > on > > this). I've just got the results back. > > > > I have high nickel and glutathione conjugates in mitochondria. > > > > Pictures showed glutathione conjugates with nickel in the > > mitochondria, that I have an odd appearance of the inside of the > > mitochondrial membrane and also few cristae in the membrane (TL > > sites are on the christae). I had a low normal magnesium and > > potassium. Calcium at the outer mitochondrial membrane was a high > > normal. Other mitochondrial results were normal (i.e. no organic > > sulphates, peptide complexes, lactic acid, keto-acids, > > organochlorides, PCBs, PBBs, dichlorobenzene, organophosphates, > > DNA/RNA). > > > > Serum liver derived glutathione-S-transferase was high - 53 (normal > > range 12-46) and red cell glutathione-S-transferase 157 (range 68- > > 167). Glutathione levels were normal at 1.94 mmmol/l . Affinity > > chromatography showed an enzyme band consistent with exposure to > > toxic metals. Atomic emission analysis showed the presence of > nickel > > in the abnormal form of the enzyme. The high serum glutathione-S- > > transferase was unusual as nickel is usually detoxified by red > cells > > and not the liver. > > > > The results mean that I have nickel poisoning and that nickel will > > be causing some energy problems. I've also got Lyme borreliosis, > > and I've heard that heavy metal problems are common with lyme. > > > > Cheers, > > Carol > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 19, 2006 Report Share Posted June 19, 2006 Hi, . As usual, that's another very good question! I was wondering this myself. Maybe her glutathione transferase enzymes are not able to carry out the conjugation process properly, including unbinding from the conjugates. Or maybe the cells have a problem exporting the conjugates. Or maybe there is more nickel than the glutathione can keep up with. I don't know. Another thing I'll have to bounce off Dr. ! Rich > > > > Hi Rich, > > > > Thanks for the reply. Please can you tell me what SNPs are? > > ***SNP stands for " single nucleotide polymorphism. " > > ***The story goes like this: In the nucleus of each human cell > (except red blood cells and a small number of other types, which > don't have nuclei) there are DNA molecules that represent about > 35,000 genes. Genes incorporate the code that tells the cell how to > make the various enzymes and other proteins it needs. The code for > one enzyme in the DNA is made up of a specific series of nucleotides > in a long chain (actually there are two complementary chains in the > double-helix structure of the DNA molecule, which have the same > information coded into each of them). There are four different > types of nucleotides, and the sequence in which they are present in > a the DNA molecule is what tells the cell what the sequence of amino > acids should be in the enzyme that is coded for. > > ***When we started with Adam and Eve, there were presumably no > mistakes in the coded sequence of nucleotides. (I realize that > everyone doesn't look at it that way, so if macroevolution is your > favorite theory, that's fine.) In any case, down through the years, > there have been mutations or changes that have occurred in the germ > line of humans. The germ line includes the sperm and ova cells that > eventually became new people down through the years. There are > several classes of changes, but one of the main classes is the SNPs, > in which only one nucleotide has been changed, which may change one > amino acid in the resulting enzyme, such as one of the glutathione > transferase enzymes. (I might mention that SNPs are being > interpreted a little more broadly than that, and can include things > like deletions of nucleotides altogether.) It is now estimated that > there are over 10 million possible SNPs in the entire human genome > of about 35,000 genes. We all have a bunch of them, inherited from > our ancestors. The only question is which ones we have. And of > course, the next question is " so what? " Lots of them don't have any > effect. Some are important enough to prevent a person from being > born alive in the first place. Others produce significant birth > defects, and some only show up if they are " provoked " by something > that goes on in a person's life, such as a toxin exposure or > exposure to some disease. > > ***The reason I brought up SNPs in connection with your glutathione > transferase enzymes is that there must be a reason why you developed > nickel toxicity. One possibility is that you had a big exposure. > Another possibility is that your detox system has genetic issues > that cause it to work less efficiently than normal. You've > established that you have enough glutathione. The next question is > whether your body can use it efficiently to take out toxins, such as > nickel. (Incidentally, I'm not sure whether glutathione conjugation > is the only route for detoxing nickel.) That may depend on whether > you have SNPs in your glutathione transferase enzymes that interfere > with their normal efficient operation. Just slowing them down some > might be enough to allow the nickel to build up. > > > > The test sheet showed glutathione and nickel separately. However, > > the notes alongside the picture said " glutathione conjugates with > > nickel " , and in the biochemist's notes at the bottom it > said " there > > are significant changes to the inner mitochondrial membrane AND > > nickel-related glutathione conjugates are present IN the > > mitochondria " . > > ***O.K., so they are hooked together. > > > > > The test used an " epifluorescence " microscope showing images > several > > orders of magnitude better than that of a conventional light > > microscope. > > ***Oh, O.K. I was pretty sure an ordinary light microscope would > not be able to resolve the detail of the mitochondria. > > > > > I've no idea how I've ended up with so much nickel in me. Nothing > > obvious. I started to get very sensitive to many of my earrings > > soon after getting the classic symptoms of Lyme borreliosis in > 1991, > > when my ME/CFS started. I do use stainless steel saucepans and > > often burn them, I wonder if they can release more nickel if burnt. > > ***I think they would. That would speed up the corrosion quite a > bit. If some of the corrosion products became incorporated in your > food, that would give you a bigger exposure. Also to chromium and > iron, which are generally beneficial. I doubt if you would eat > burnt food, and no doubt you scrub the pans after they get burnt. > The next time you used them, though, they would probably release > some nickel and iron until the new chromium-oxide-rich protective > layer formed on the surface of the metal. > > > I'll start using glass saucepans I think. I would guess that it is > > something about me that can't detox nickel properly. > > ***I'm suspecting that, too. Glass is pretty inert. At least it > doesn't contain nickel. > > Another > > potential source would be my amalgam fillings, however my dentist > > told me that nickel has not been put in fillings for a long time > and > > he didn't think I could have any nickel in mine. I am going to > > reclarify this with him as I had some very old fillings about 25 > > years old that were leaking recently (a splint I was wearing went > > black in parts from leakage of the fillings). I've recently had > my > > amalgams removed. > > ***The old fillings do seem like a possibility. > > > > I have also had thyroid problems, low TSH and lowish T4/T3 and > > goitre - I believe heavy metals can suppress both TSH and T4/T3 at > > the same time. I also have nickel DNA adducts. The biochemist > > believes these may have been formed by an allergy to glutathione > > conjugates to nickel - my system was kicking off the nickel from > the > > glutathione which was then attaching to DNA. > > > > One very interesting thing - the biochemist studied my glutathione- > S- > > transferase in detail around 7 years ago. Affinity chromatography > > of the serum liver derived enzyme showed evidence of tissue > > breakdown (estrogenic tissue) and not nickel or heavy metals. The > > red blood cell enzyme was normal - no nickel etc. This raises > lots > > of questions - have I been exposed to lots of nickel or not > detoxing > > it properly since 7 years ago? - or did I have lots of nickel a > > while back but it was not being conjugated at the time of the > test, > > but for some reason it is being conjugated now? My health is > > slightly better now than 7 years ago. > > ***I'm not sure what to make of this. > > > > I have been doing FIR saunaing twice a week since January and so I > > suppose I could be mobilising nickel. I had my amalgams removed > > last autumn and have been taking platinum plus (free form amino > > acids with a small bit of MSM), lipoceutical glutathione and Humet > R > > (minerals with humic and fulvic acid) so maybe these things are > > boosting the gluathione transferase. > > ***I don't know. > > > > I'm trying to think of anything that could have given me nickel > > poisoning during the last 7 years. I have changed stainless steel > > pans and my amalgams started leaking. I had stopped wearing > > jewellery many years ago but now wear a supposedly copper bracelet > > with magnets in it. My diet has been similar - I removed junk > foods > > many years ago, but some supplements have changed. > > > > Another interesting thing that has happened to me is that after I > > started borrelia treatments (with herbs - including Samento) I > > started getting more breast cysts and the fluid inside them was > > black with a dark green > > tinge). I had had breast cysts before but the fluid was a brown > > colour. I am now not herxing as badly and can cope with much higher > > doses of antiborrelial herbs (Samento plus chinese herbs), and the > > fluid in the most recent cyst > > 2 or 3 months ago was not black but was brown again. I wrote to the > > biochemist a while back and asked him what could cause the > > black/green colour and he said bacterial infection or nickel were > the > > only things he knew of. I would guess it was the nickel as I > > haven't heard of borrelia causing black fluid - which could > indicate > > that herxing from borrelia treatment was possibly affecting nickel > > detox in some way. Nickel can be estrogenic, by the way, so could > > easily end up in breast tissue. > > Hmmm. Do you mean cysts that form on the surface of the skin, or > are you talking about cysts inside the breasts, that have to be > removed surgically? In any case, they don't sound like a lot of fun. > > > > > Would you know if glutathione-S-transferase is used to detox > > borrelia toxins? > > ***No, I don't. > > I was not herxing at the time of the translocator > > test so not stressing the system so much. Do you know if there is > a > > link between heavy metal poisoning and Lyme? > > ***I do know that Borrelia depletes cysteine and glutathione, and > since glutathione is necessary to detox heavy metals, it would make > sense that they would build up if Borrelia infection is present. > > I know some LLMDs say > > they find heavy metal poisoning quite often in Lymies. > > ***I think that would make sense, except you tested normal for > glutathione. > > > > > If ADP is not converted to ATP on the TL protein, would you have > any > > idea how blockage of the " active TL site " could reduce ADP to ATP > > conversion. > > ***It may be a bottleneck effect. If the ADP and ATP cannot be > transported in and out of the mitochondria, respectively, fast > enough, then that would limit the rate of conversion of ADP to ATP, > because there wouldn't be enough ADP present in the mitochondria at > a given time to convert to ATP, even though the machinery in the > mitochondria might be perfectly ready to do it. > > > > Cheers, > > Carol > > > ***Cheers to you, too! > > ***Rich > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 19, 2006 Report Share Posted June 19, 2006 Rich, I profess ignorance on this new test. But I will ask my dumb question anyway. <grin> What if the person is infected with babesia - a chronic infection inside red blood cells? How is this going to relate to genetics in other cells? a > > Hi, . > > The translocator test is actually done on neutrophils, rather than > red blood cells. Red blood cells do not have mitochondria. They > derive their biochemical energy (ATP) from glycolysis. > > Neutrophils are the most abundant of the white blood cells, and they > have mitochondria, so I suspect that's the reason Dr. has > chosen to study them. They are the most conveniently sampled cells > that have mitochondria. > > The life span of neutrophils is actually even less than that of red > blood cells. Neutrophils last only a few days. New ones are > produced in the bone marrow. > > It's a good question. To what degree do the mitochondria in > neutrophils represent what is happening in the mitochondria of soft > tissue, such as muscle? For toxins that are fairly mobile in the > body or for current exposures, the test would seem to be fine. I > suppose it's possible that some toxins from exposures in the past > would be so well sequestered in the tissues that they would not show > up in the neutrophils. You mentioned mercury, and it is known that > mercury does not stay in the blood very long. > > I'll have to ask Dr. if he has done any correlations with > mitochondria from muscle biopsies, for example. > > Rich > > > > > > > > Hi, > > > > > > A while back I posted that I have a very poor conversion of ADP > to > > > ATP and part of that was thought to be caused by receptor site > > > blockage. > > > > > > I've recently had the translocator test done which looks at the > > > mitochondrial membrane and translocator protein (TL)(TL is used > to > > > transport ATP and ADP across the mitochondiral membrane - I > think > > it > > > might be the site of ADP to ATP conversion too, but not 100% > sure > > on > > > this). I've just got the results back. > > > > > > I have high nickel and glutathione conjugates in mitochondria. > > > > > > Pictures showed glutathione conjugates with nickel in the > > > mitochondria, that I have an odd appearance of the inside of the > > > mitochondrial membrane and also few cristae in the membrane (TL > > > sites are on the christae). I had a low normal magnesium and > > > potassium. Calcium at the outer mitochondrial membrane was a high > > > normal. Other mitochondrial results were normal (i.e. no organic > > > sulphates, peptide complexes, lactic acid, keto-acids, > > > organochlorides, PCBs, PBBs, dichlorobenzene, organophosphates, > > > DNA/RNA). > > > > > > Serum liver derived glutathione-S-transferase was high - 53 > (normal > > > range 12-46) and red cell glutathione-S-transferase 157 (range > 68- > > > 167). Glutathione levels were normal at 1.94 mmmol/l . Affinity > > > chromatography showed an enzyme band consistent with exposure to > > > toxic metals. Atomic emission analysis showed the presence of > > nickel > > > in the abnormal form of the enzyme. The high serum glutathione- S- > > > transferase was unusual as nickel is usually detoxified by red > > cells > > > and not the liver. > > > > > > The results mean that I have nickel poisoning and that nickel > will > > > be causing some energy problems. I've also got Lyme borreliosis, > > > and I've heard that heavy metal problems are common with lyme. > > > > > > Cheers, > > > Carol > > > > > > > > > > > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 20, 2006 Report Share Posted June 20, 2006 Hi and all, I was wondering whether I was detoxing the nickel with the conjugates myself. I'm finding that the more tests I get done the more questions are raised. I have been taking supplements which would support my glutathione-S- transferase function, so it is always possible that I am just detoxing it better. I also have nickel DNA adducts and I asked the biochemist how I thought they could have occured and he said either losing weight quickly and mobilising too much nickel in organic form (I hadn't lost weight) or I could be allergic to the glutathione nickel conjugates and I could be kicking the nickel off the conjugates which is then attaching to DNA - so I suppose there is the possiblity that I am not conjugating properly. I am on chinese herbals at the moment to treat Lyme borreliosis and they modulate my immune system very well. Many years ago in 1992 when I first got ill, the herbs stopped me reacting to my earrings, which is now thought to have been nickel allergy. So its possible the herbs could now be dampening down any allergy respone to nickel- but I'm just guessing here. I am going to get my DNA adducts and SODase remeasured again in a month or so, as I have been FIR saunaing to try and get rid of them. Maybe the results will give a clue. My gut feel about this is that I may be mobilising a little nickel through saunaing and I am detoxing it. My health has been improving slightly, however I am sometimes more brain fogged 12-24 hours after the sauna. By the way, a few years ago when I had a slightly high glutathione-S- transferase due to tissue breakdown, the biochemist said that taking glutathione may be worth a go (he suggested whey or L-glutathione with precursors taken orally). He said that cos my glutathione was being used up by detoxing the tissue breakdwon there would be less available elsewhere. Cheers, Carol > > > > Hi Rich, > > > > Thanks for the reply. Please can you tell me what SNPs are? > > ***SNP stands for " single nucleotide polymorphism. " > > ***The story goes like this: In the nucleus of each human cell > (except red blood cells and a small number of other types, which > don't have nuclei) there are DNA molecules that represent about > 35,000 genes. Genes incorporate the code that tells the cell how to > make the various enzymes and other proteins it needs. The code for > one enzyme in the DNA is made up of a specific series of nucleotides > in a long chain (actually there are two complementary chains in the > double-helix structure of the DNA molecule, which have the same > information coded into each of them). There are four different > types of nucleotides, and the sequence in which they are present in > a the DNA molecule is what tells the cell what the sequence of amino > acids should be in the enzyme that is coded for. > > ***When we started with Adam and Eve, there were presumably no > mistakes in the coded sequence of nucleotides. (I realize that > everyone doesn't look at it that way, so if macroevolution is your > favorite theory, that's fine.) In any case, down through the years, > there have been mutations or changes that have occurred in the germ > line of humans. The germ line includes the sperm and ova cells that > eventually became new people down through the years. There are > several classes of changes, but one of the main classes is the SNPs, > in which only one nucleotide has been changed, which may change one > amino acid in the resulting enzyme, such as one of the glutathione > transferase enzymes. (I might mention that SNPs are being > interpreted a little more broadly than that, and can include things > like deletions of nucleotides altogether.) It is now estimated that > there are over 10 million possible SNPs in the entire human genome > of about 35,000 genes. We all have a bunch of them, inherited from > our ancestors. The only question is which ones we have. And of > course, the next question is " so what? " Lots of them don't have any > effect. Some are important enough to prevent a person from being > born alive in the first place. Others produce significant birth > defects, and some only show up if they are " provoked " by something > that goes on in a person's life, such as a toxin exposure or > exposure to some disease. > > ***The reason I brought up SNPs in connection with your glutathione > transferase enzymes is that there must be a reason why you developed > nickel toxicity. One possibility is that you had a big exposure. > Another possibility is that your detox system has genetic issues > that cause it to work less efficiently than normal. You've > established that you have enough glutathione. The next question is > whether your body can use it efficiently to take out toxins, such as > nickel. (Incidentally, I'm not sure whether glutathione conjugation > is the only route for detoxing nickel.) That may depend on whether > you have SNPs in your glutathione transferase enzymes that interfere > with their normal efficient operation. Just slowing them down some > might be enough to allow the nickel to build up. > > > > The test sheet showed glutathione and nickel separately. However, > > the notes alongside the picture said " glutathione conjugates with > > nickel " , and in the biochemist's notes at the bottom it > said " there > > are significant changes to the inner mitochondrial membrane AND > > nickel-related glutathione conjugates are present IN the > > mitochondria " . > > ***O.K., so they are hooked together. > > > > > The test used an " epifluorescence " microscope showing images > several > > orders of magnitude better than that of a conventional light > > microscope. > > ***Oh, O.K. I was pretty sure an ordinary light microscope would > not be able to resolve the detail of the mitochondria. > > > > > I've no idea how I've ended up with so much nickel in me. Nothing > > obvious. I started to get very sensitive to many of my earrings > > soon after getting the classic symptoms of Lyme borreliosis in > 1991, > > when my ME/CFS started. I do use stainless steel saucepans and > > often burn them, I wonder if they can release more nickel if burnt. > > ***I think they would. That would speed up the corrosion quite a > bit. If some of the corrosion products became incorporated in your > food, that would give you a bigger exposure. Also to chromium and > iron, which are generally beneficial. I doubt if you would eat > burnt food, and no doubt you scrub the pans after they get burnt. > The next time you used them, though, they would probably release > some nickel and iron until the new chromium-oxide-rich protective > layer formed on the surface of the metal. > > > I'll start using glass saucepans I think. I would guess that it is > > something about me that can't detox nickel properly. > > ***I'm suspecting that, too. Glass is pretty inert. At least it > doesn't contain nickel. > > Another > > potential source would be my amalgam fillings, however my dentist > > told me that nickel has not been put in fillings for a long time > and > > he didn't think I could have any nickel in mine. I am going to > > reclarify this with him as I had some very old fillings about 25 > > years old that were leaking recently (a splint I was wearing went > > black in parts from leakage of the fillings). I've recently had > my > > amalgams removed. > > ***The old fillings do seem like a possibility. > > > > I have also had thyroid problems, low TSH and lowish T4/T3 and > > goitre - I believe heavy metals can suppress both TSH and T4/T3 at > > the same time. I also have nickel DNA adducts. The biochemist > > believes these may have been formed by an allergy to glutathione > > conjugates to nickel - my system was kicking off the nickel from > the > > glutathione which was then attaching to DNA. > > > > One very interesting thing - the biochemist studied my glutathione- > S- > > transferase in detail around 7 years ago. Affinity chromatography > > of the serum liver derived enzyme showed evidence of tissue > > breakdown (estrogenic tissue) and not nickel or heavy metals. The > > red blood cell enzyme was normal - no nickel etc. This raises > lots > > of questions - have I been exposed to lots of nickel or not > detoxing > > it properly since 7 years ago? - or did I have lots of nickel a > > while back but it was not being conjugated at the time of the > test, > > but for some reason it is being conjugated now? My health is > > slightly better now than 7 years ago. > > ***I'm not sure what to make of this. > > > > I have been doing FIR saunaing twice a week since January and so I > > suppose I could be mobilising nickel. I had my amalgams removed > > last autumn and have been taking platinum plus (free form amino > > acids with a small bit of MSM), lipoceutical glutathione and Humet > R > > (minerals with humic and fulvic acid) so maybe these things are > > boosting the gluathione transferase. > > ***I don't know. > > > > I'm trying to think of anything that could have given me nickel > > poisoning during the last 7 years. I have changed stainless steel > > pans and my amalgams started leaking. I had stopped wearing > > jewellery many years ago but now wear a supposedly copper bracelet > > with magnets in it. My diet has been similar - I removed junk > foods > > many years ago, but some supplements have changed. > > > > Another interesting thing that has happened to me is that after I > > started borrelia treatments (with herbs - including Samento) I > > started getting more breast cysts and the fluid inside them was > > black with a dark green > > tinge). I had had breast cysts before but the fluid was a brown > > colour. I am now not herxing as badly and can cope with much higher > > doses of antiborrelial herbs (Samento plus chinese herbs), and the > > fluid in the most recent cyst > > 2 or 3 months ago was not black but was brown again. I wrote to the > > biochemist a while back and asked him what could cause the > > black/green colour and he said bacterial infection or nickel were > the > > only things he knew of. I would guess it was the nickel as I > > haven't heard of borrelia causing black fluid - which could > indicate > > that herxing from borrelia treatment was possibly affecting nickel > > detox in some way. Nickel can be estrogenic, by the way, so could > > easily end up in breast tissue. > > Hmmm. Do you mean cysts that form on the surface of the skin, or > are you talking about cysts inside the breasts, that have to be > removed surgically? In any case, they don't sound like a lot of fun. > > > > > Would you know if glutathione-S-transferase is used to detox > > borrelia toxins? > > ***No, I don't. > > I was not herxing at the time of the translocator > > test so not stressing the system so much. Do you know if there is > a > > link between heavy metal poisoning and Lyme? > > ***I do know that Borrelia depletes cysteine and glutathione, and > since glutathione is necessary to detox heavy metals, it would make > sense that they would build up if Borrelia infection is present. > > I know some LLMDs say > > they find heavy metal poisoning quite often in Lymies. > > ***I think that would make sense, except you tested normal for > glutathione. > > > > > If ADP is not converted to ATP on the TL protein, would you have > any > > idea how blockage of the " active TL site " could reduce ADP to ATP > > conversion. > > ***It may be a bottleneck effect. If the ADP and ATP cannot be > transported in and out of the mitochondria, respectively, fast > enough, then that would limit the rate of conversion of ADP to ATP, > because there wouldn't be enough ADP present in the mitochondria at > a given time to convert to ATP, even though the machinery in the > mitochondria might be perfectly ready to do it. > > > > Cheers, > > Carol > > > ***Cheers to you, too! > > ***Rich > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 21, 2006 Report Share Posted June 21, 2006 Hi Carol Thanks to you (and others who have joined in the discussion) for all the information concerning nickel. My daughter (23 years, ME/CFS since 2001) also has a nickel problem, although in her case we know of the problem only through lymphocyte nickel sensitivity tests. I was very interested and also concerned to see from your post that nickel can end up in the mitochondria, and looked for information about this. So far I didn`t find anything on nickel specifically, but I have found an article which concerns ultrafine particles (UFP). The ultrafine particles seem to be released into the air for instance during fuel combustion (e.g. car exhaust). They get deep down in the lungs and from there into the bloodstream. The article mentions the content of metals in the UFPs. It seems from other articles that I have read that nickel can be one of the metals found in ultrafine particles. The article is: " Ultrafine Particulate Pollutants Induce Oxidative Stress and Mitochondrial Damage " http://tinyurl.com/f3yvv There are photos of the ultrafine particles inside mitochondria, photos of damaged cristae, and of damaged mitochondria. I hope you will post as you find out more, especially I hope you find solutions for detoxification and prevention. Wishing you all the best ne > > I have high nickel and glutathione conjugates in mitochondria. > > Pictures showed glutathione conjugates with nickel in the > mitochondria, that I have an odd appearance of the inside of the > mitochondrial membrane and also few cristae in the membrane (TL > sites are on the christae). Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 21, 2006 Report Share Posted June 21, 2006 I think that is a good piece of research. It makes so much sense that the pollution we endure would go ultimately to such a deep, basic level as the mitochondria. My gut says that explains a whole host of ills. I would go so far as to say it is a defining aspect of life in an industrialized society. But that is just my gut. Adrienne Re: Mitochondrial function - my translocator test results Hi Carol Thanks to you (and others who have joined in the discussion) for all the information concerning nickel. My daughter (23 years, ME/CFS since 2001) also has a nickel problem, although in her case we know of the problem only through lymphocyte nickel sensitivity tests. I was very interested and also concerned to see from your post that nickel can end up in the mitochondria, and looked for information about this. So far I didn`t find anything on nickel specifically, but I have found an article which concerns ultrafine particles (UFP). The ultrafine particles seem to be released into the air for instance during fuel combustion (e.g. car exhaust). They get deep down in the lungs and from there into the bloodstream. The article mentions the content of metals in the UFPs. It seems from other articles that I have read that nickel can be one of the metals found in ultrafine particles. The article is: " Ultrafine Particulate Pollutants Induce Oxidative Stress and Mitochondrial Damage " http://tinyurl.com/f3yvv There are photos of the ultrafine particles inside mitochondria, photos of damaged cristae, and of damaged mitochondria. I hope you will post as you find out more, especially I hope you find solutions for detoxification and prevention. Wishing you all the best ne > > I have high nickel and glutathione conjugates in mitochondria. > > Pictures showed glutathione conjugates with nickel in the > mitochondria, that I have an odd appearance of the inside of the > mitochondrial membrane and also few cristae in the membrane (TL > sites are on the christae). This list is intended for patients to share personal experiences with each other, not to give medical advice. If you are interested in any treatment discussed here, please consult your doctor. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 22, 2006 Report Share Posted June 22, 2006 Hi, I spoke to my doc today. She thinks that the high nickel-glutathione conjugates means that I am detoxifying the nickel. She said something about sometimes some glutathione will detach from the conjugates, but wasn't concerned about that. She also agrees with my suggestion that I could be remobilising some nickel with my FIR saunaing. Its a mystery to her too why nickel didn't come up in the glutathione-S- transferase tests 7 years ago. So it is unknown whether the nickel is a newish problem or not. She did say that it may be possible for some chemicals that has been lying around in tissues out of the way for a long time to start being detoxified at a later time. Cheers, Carol > > Hi Rich and CArol, > Wouldn't the fact that the nickel is bound to glutathione mean it is in > the process of being detoxified and so CArol's body is capable of > detoxifiying it ? > > > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 22, 2006 Report Share Posted June 22, 2006 Hi Carol Thanks for sharing your results. I also have recently had the CFS profile done by Dr . My SODase result is low at 39% and indicates a deficiency of Zinc and Copper. My ADP to ATP conversion (whole cells)is rather poor. My Translocator Protein in is normal but TP out is rather poor. Can you tell me if you requested further investigation of the TP problem or did your Dr recommend it? Thanks > > Hi, > > A while back I posted that I have a very poor conversion of ADP to > ATP and part of that was thought to be caused by receptor site > blockage. > > I've recently had the translocator test done which looks at the > mitochondrial membrane and translocator protein (TL)(TL is used to > transport ATP and ADP across the mitochondiral membrane - I think it > might be the site of ADP to ATP conversion too, but not 100% sure on > this). I've just got the results back. > > I have high nickel and glutathione conjugates in mitochondria. > > Pictures showed glutathione conjugates with nickel in the > mitochondria, that I have an odd appearance of the inside of the > mitochondrial membrane and also few cristae in the membrane (TL > sites are on the christae). I had a low normal magnesium and > potassium. Calcium at the outer mitochondrial membrane was a high > normal. Other mitochondrial results were normal (i.e. no organic > sulphates, peptide complexes, lactic acid, keto-acids, > organochlorides, PCBs, PBBs, dichlorobenzene, organophosphates, > DNA/RNA). > > Serum liver derived glutathione-S-transferase was high - 53 (normal > range 12-46) and red cell glutathione-S-transferase 157 (range 68- > 167). Glutathione levels were normal at 1.94 mmmol/l . Affinity > chromatography showed an enzyme band consistent with exposure to > toxic metals. Atomic emission analysis showed the presence of nickel > in the abnormal form of the enzyme. The high serum glutathione-S- > transferase was unusual as nickel is usually detoxified by red cells > and not the liver. > > The results mean that I have nickel poisoning and that nickel will > be causing some energy problems. I've also got Lyme borreliosis, > and I've heard that heavy metal problems are common with lyme. > > Cheers, > Carol > Quote Link to comment Share on other sites More sharing options...
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