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trish,

I think it's always best to take aminos with food, and with a wide spectrum

of other aminos, just as we do in nature. They can be taken in isolation for

various therapeutic purposes but the theoretical risks increase in that

case. Tyrosine and phenylalanine for example can raise blood pressure in

some people, and as we've alluded to here recently cysteine is hazardous to

nerve cells via its conversion to cysteic acid and cysteine sulfinic acid

(both excitotoxins). Glutamic acid (glutamate) and aspartate are also

excitotoxins, and there are certainly other risks inherent in other aminos

as well. But those risks are relatively small and significant only when

taken in high concentrations, especially on an empty stomach.

I'm not aware of any specific amino combinations that are more hazardous

than the individual aminos taken separately.

-gts

> amino's

>

>

> I'm trying to determine which amino's interfere pathways of other

> amino's. ... various recommended protocols suggest that we take

> single & combo aminos on an empty stomach... as I understand it,

> some of he reasons relate to pathway interference, & some

> reasons relate to interference from hormonal/body activities that

> are the result of eating. Are there any definie no-no's in amino

> combo's? Does know where I could find that information?

> Thank you for any thoughts.

> Trishj

>

>

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On Thu, 21 Jun 2001 06:56:24 -0400

" trish " <zedora@...> wrote:

> I'm trying to determine which amino's interfere pathways

> of other amino's. ... various recommended protocols

> suggest that we take single & combo aminos on an empty

> stomach... as I understand it, some of he reasons relate

> to pathway interference, & some reasons relate to

> interference from hormonal/body activities that are the

> result of eating. Are there any definie no-no's in amino

> combo's? Does know where I could find that

> information? Thank you for any thoughts.

> Trishj

>

Amino acids may be categorized as large or small and polar

or non-polar. Each of the resultant sub-categories has a

separate transporter through the blood-brain barrier. Those

transporters are all downregulated by insulin while a

separate transporter specific to tryptophan is insulin

dependent.

If one seeks the highest peak level of an ingested isolated

amino acid in the brain, one should not consume it with any

other amino acid that falls in the same sub-category. I'll

try to find my old reference but do recollect arginine,

ornithine and lysine to be in the same subcategory. That

argues against the GH-releasing mixes that include lysine.

On the average 40-42% of ingested amino acids are deaminated

and converted to glucose in the liver. A large bolus of any

amino-acid mix will yield an insulin spike driven by the

glucose availability. That spike will reduce the peak

concentration of any ingested amino acid other than

tryptophan. For that reason, one might choose not to combine

aminos regardless of subclass if the resulting dose is more

than a few grams.

The latter effect is probably protective in that glutamine

and glutamate are most prone to be deaminated. The supposed

excitotoxic effects of consuming either in quantity may well

be opposed by reduced transport and by parallel increases in

availability of glucose and tryptophan. This is clearly an

area for in-vivo research.

For muscles, insulin enhances the absorption and utilization

of all amino acids. Combining carbs with protein after a

workout is a good idea.

Only combine aminos with other food if you are compensating

for the shortage of a limiting amino acid in that other

food. Tissues, especially muscle can't hold much free-aminos

but can create protein at an amazing rate. Aminos can be

used as drugs or as protein building blocks. The latter

preempts the former. An expensive amino mixed with all the

others required to build muscle proteins (for instance) will

be rapidly dissipated. It will not do so if those other

required aminos aren't present. Coingested food also

competes for transport from the gut and will delay

absorption of the expensive amino.

One obvious area of research would be to determine whether a

relatively cheap product that the liver readily degrades

(such as glutamine) could saturate the liver enzymes and

sacrificially protect a more expensive product such as

L-carnosine from degradation.

Bob Cruder

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On Thu, 21 Jun 2001 06:56:24 -0400

" trish " <zedora@...> wrote:

> I'm trying to determine which amino's interfere pathways

> of other amino's. ... various recommended protocols

> suggest that we take single & combo aminos on an empty

> stomach... as I understand it, some of he reasons relate

> to pathway interference, & some reasons relate to

> interference from hormonal/body activities that are the

> result of eating. Are there any definie no-no's in amino

> combo's? Does know where I could find that

> information? Thank you for any thoughts.

> Trishj

>

Amino acids may be categorized as large or small and polar

or non-polar. Each of the resultant sub-categories has a

separate transporter through the blood-brain barrier. Those

transporters are all downregulated by insulin while a

separate transporter specific to tryptophan is insulin

dependent.

If one seeks the highest peak level of an ingested isolated

amino acid in the brain, one should not consume it with any

other amino acid that falls in the same sub-category. I'll

try to find my old reference but do recollect arginine,

ornithine and lysine to be in the same subcategory. That

argues against the GH-releasing mixes that include lysine.

On the average 40-42% of ingested amino acids are deaminated

and converted to glucose in the liver. A large bolus of any

amino-acid mix will yield an insulin spike driven by the

glucose availability. That spike will reduce the peak

concentration of any ingested amino acid other than

tryptophan. For that reason, one might choose not to combine

aminos regardless of subclass if the resulting dose is more

than a few grams.

The latter effect is probably protective in that glutamine

and glutamate are most prone to be deaminated. The supposed

excitotoxic effects of consuming either in quantity may well

be opposed by reduced transport and by parallel increases in

availability of glucose and tryptophan. This is clearly an

area for in-vivo research.

For muscles, insulin enhances the absorption and utilization

of all amino acids. Combining carbs with protein after a

workout is a good idea.

Only combine aminos with other food if you are compensating

for the shortage of a limiting amino acid in that other

food. Tissues, especially muscle can't hold much free-aminos

but can create protein at an amazing rate. Aminos can be

used as drugs or as protein building blocks. The latter

preempts the former. An expensive amino mixed with all the

others required to build muscle proteins (for instance) will

be rapidly dissipated. It will not do so if those other

required aminos aren't present. Coingested food also

competes for transport from the gut and will delay

absorption of the expensive amino.

One obvious area of research would be to determine whether a

relatively cheap product that the liver readily degrades

(such as glutamine) could saturate the liver enzymes and

sacrificially protect a more expensive product such as

L-carnosine from degradation.

Bob Cruder

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Another question Bob,

When taking L Carnosine (1 gr) in the mornings on an empty stomach, am I

simplly wasting it? Also, it produces a tingling sensation in my arms and

legs not unlike a very minor Niacin flush. This lasts for 1 1/2 hours.

(definitely Carnosine dependent, as when I don't take it I don't have this

very noticible reaction) Does this mean that it is being absorbed?

Any illumination appreciated! And thanks for the very clear explanation of

how Aminos work in tandem and with food.

MM

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Get your FREE download of MSN Explorer at http://explorer.msn.com

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That's the same response I recieved from l-carnosine ( 0.500g) - I was a

little alarmed by this and I have not tried it since, does anyone know if

this is a neutral side effect?

Re: amino's

> Another question Bob,

> When taking L Carnosine (1 gr) in the mornings on an empty stomach, am I

> simplly wasting it? Also, it produces a tingling sensation in my arms and

> legs not unlike a very minor Niacin flush. This lasts for 1 1/2 hours.

> (definitely Carnosine dependent, as when I don't take it I don't have this

> very noticible reaction) Does this mean that it is being absorbed?

> Any illumination appreciated! And thanks for the very clear explanation of

> how Aminos work in tandem and with food.

> MM

>

> _________________________________________________________________

> Get your FREE download of MSN Explorer at http://explorer.msn.com

>

>

>

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WOW ! I have been taking carnosine for about 6 months had have terrible

flushing..my doctor said it was rosacea..which is a name they give facial

flushing when they can not figure out why. I would like to know if you get

flushing too?? I get it again about 4 hours after I take it when I eat

lunch. Would love to hear back from you..

Re: amino's

>

>

> > Another question Bob,

> > When taking L Carnosine (1 gr) in the mornings on an empty stomach, am I

> > simplly wasting it? Also, it produces a tingling sensation in my arms

and

> > legs not unlike a very minor Niacin flush. This lasts for 1 1/2 hours.

> > (definitely Carnosine dependent, as when I don't take it I don't have

this

> > very noticible reaction) Does this mean that it is being absorbed?

> > Any illumination appreciated! And thanks for the very clear explanation

of

> > how Aminos work in tandem and with food.

> > MM

> >

> > _________________________________________________________________

> > Get your FREE download of MSN Explorer at http://explorer.msn.com

> >

> >

> >

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I need to clarify - I do not get the redness/flushing, however, I do get the

tingling sensation in my forearms and thighs for about 60 minutes.

Re: amino's

> >

> >

> > > Another question Bob,

> > > When taking L Carnosine (1 gr) in the mornings on an empty stomach, am

I

> > > simplly wasting it? Also, it produces a tingling sensation in my arms

> and

> > > legs not unlike a very minor Niacin flush. This lasts for 1 1/2 hours.

> > > (definitely Carnosine dependent, as when I don't take it I don't have

> this

> > > very noticible reaction) Does this mean that it is being absorbed?

> > > Any illumination appreciated! And thanks for the very clear

explanation

> of

> > > how Aminos work in tandem and with food.

> > > MM

> > >

> > > _________________________________________________________________

> > > Get your FREE download of MSN Explorer at http://explorer.msn.com

> > >

> > >

> > >

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Dear ,

No facial flushing, just the tingling. Who knows? Maybe it is harmless. But

then again, carnosine hasn't been tested thoroughly in humans, just rodents

and in vitro.

Best wishes

MM

_________________________________________________________________

Get your FREE download of MSN Explorer at http://explorer.msn.com

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On Fri, 22 Jun 2001 08:01:40 -0000

" Mambo Mambo " <mambomambo@...> wrote:

> When taking L Carnosine (1 gr) in the mornings on an

> empty stomach, am I

> simplly wasting it?

LEF claims that small doses are degraded by carnosinase in

liver but that large doses such as yours saturate the

liver's metabolic capacity and largely survive. I originally

questioned this but they did follow up with enough murine

studies to justify the dosage.

>Also, it produces a tingling

> sensation in my arms and

> legs not unlike a very minor Niacin flush. This lasts for

> 1 1/2 hours.

> (definitely Carnosine dependent, as when I don't take it

> I don't have this

> very noticible reaction) Does this mean that it is being

> absorbed?

I can't say whether your reacting to the carnosine itself or

to a metabolite. I get a niacin-like flush from both GABA

and glycine but need at least a 2-gram dosage of either.

I do have a hypothesis. Carnosine is a dipeptide

made up of the amino acids beta-alanine and l-histidine.

L-histidine is the precursor from which the body synthesizes

histamine. Histamine is what is normally released from mast

cells in response to injury or allergens. It is also

released by a few chemical triggers such as capsaicin from

red pepper or fast-release niacin.

My guess is that carnosine is breaking down somewhere and

the body is unable to store the free histidine so it gets

converted into histamine. For my hypothesis to be correct,

the rate-limiter for histamine production must be the

availability of L-histidine. I can't think of any other

synthesis that doesn't have a controlling feedback loop.

Another related hypothesis is that L-carnosine doesn't

normally circulate in the plasma. The liver doesn't normally

destroy desirable products. L-carnosine is probably

synthesized within the target cells. Your symptom may be

telling you that the L-carnosine is making it to locations

where it would not otherwise be present.

The information on carnosine available at www.lef.org has

expanded significantly since my last visit. I've got to give

them credit for all the research citations and the mix of

in-vivo with in-vitro. Thanks for reminding me about

L-carnosine. I'm impressed enough to add it back to my

personal protocol. I still have an unopened bottle of powder

from Beyond-A-Century which (for now) is the lowest-cost

provider.

I also found some interesting quotes there:

" Glutamate binding to its cellular receptors nearly doubled

in the carnosine treated group. Since glutamate is the main

excitatory neurotransmitter, this may explain the more

normal behavioral reactivity of the carnosine-fed mice. "

" Carnosine and glutamate are found together in presynaptic

terminals in the brain. Experimental evidence shows that

carnosine protects cells against excitotoxic death,

supporting the notion that carnosine serves the same purpose

in the brain. An interesting Russian study showed that rat

cerebellar cells incubated in carnosine were resistant to

excitotoxic cell death from the glutamate analogs NMDA and

kainite (Boldyrev A et al.,1999). "

The above continues to build my personal hypothesis that

glutamate is a net plus for brain function and that

excitotoxicity depends on hypoxia or lack of protective

factors. One might want to temporarily reduce glutamate

activity in the latter situations but to do so in general is

to induce senescent behavior sooner.

Bob Cruder

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  • 1 year later...

I am posting about this again because it's driving me crazy. Every time I

take my amino's they feeds my bad bacteria and I feel terrible. Is this just

something I have to deal with or have some of you found a good amino acid

supplement (not whey) that does not do this and does not make you feel

terrible?

I need to take amino's to help with detoxing and muscle building and with

everything else they are supposed to do. I feel better in the area's I just

mentioned when taking amino's but I can't stand how my stomach feels when I

take them because the amino's feed my bad bacteria. Thank you,

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I can't stand how my stomach feels when I

> take them because the amino's feed my bad bacteria. Thank you,

, I take LPP brand of predigested protein, 3 grams a day but I

do not know if predigested protein still feeds the bad bacteria??

Bob

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