Guest guest Posted July 1, 2007 Report Share Posted July 1, 2007 A New Line Of Communication Between Nervous System Cells Discovered By Weizmann Scientists Main Category: Neurology / Neuroscience News Article Date: 30 Jun 2007 - 13:00 PDT In a host of neurological diseases, including multiple sclerosis (MS) and several neuropathies, the protective covering surrounding the nerves - an insulating material called myelin - is damaged. Scientists at the Weizmann Institute of Science have now discovered an important new line of communication between nervous system cells that is crucial to the development of myelinated nerves - a discovery that may aid in restoring the normal function of the affected nerve fibers. Nerve cells (neurons) have long, thin extensions called axons that can reach up to a meter and or more in length. Often, these extensions are covered by myelin, which is formed by a group of specialized cells called glia. Glial cells revolve around the axon, laying down the myelin sheath in segments, leaving small nodes of exposed nerve in between. More than just protection for the delicate axons, the myelin covering allows nerve signals to jump instantaneously between nodes, making the transfer of these signals quick and efficient. When myelin is missing or damaged, the nerve signals can't skip properly down the axons, leading to abnormal function of the affected nerve and often to its degeneration. In research published recently in Nature Neuroscience, Weizmann Institute scientists Prof. Elior Peles, graduate student Ivo Spiegel, and their colleagues in the Molecular Cell Biology Department and in the United States, have now provided a vital insight into the mechanism by which glial cells recognize and myelinate axons. How do the glial cells and the axon coordinate this process " The Weizmann Institute team found a pair of proteins that pass messages from axons to glial cells. These proteins, called Necl1 and Necl4, belong to a larger family of cell adhesion molecules, so called because they sit on the outer membranes of cells and help them to stick together. Peles and his team discovered that even when removed from their cells, Necl1, normally found on the axon surface, and Necl4, which is found on the glial cell membrane, adhere tightly together. When these molecules are in their natural places, they not only create physical contact between axon and glial cell, but also serve to transfer signals to the cell interior, initiating changes needed to undertake myelination. The scientists found that production of Necl4 in the glial cells rises when they come into close contact with an unmyelinated axon, and as the process of myelination begins. They observed that if Necl4 is absent in the glial cells, or if they blocked the attachment of Necl4 to Necl1, the axons that were contacted by glial cells did not myelinate. In the same time period, myelin wrapping was already well underway around most of the axons in the control group. " What we've discovered is a completely new means of communication between these nervous system cells, " says Peles. " The drugs now used to treat MS and other degenerative diseases in which myelin is affected can only slow the disease, but not stop or cure it. Today, we can't reverse the nerve damage caused by these disorders. But if we can understand the mechanisms that control the process of wrapping the axons by their protective sheath, we might be able to recreate that process in patients. " ### http://www.medicalnewstoday.com/medicalnews.php?newsid=75315 & nfid=rssfeeds Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2007 Report Share Posted July 2, 2007 Well said! There are so many people just waiting for miracle cures from toxic drugs when the answer is to give your body the nutrition it needs and in time it will heal itself!! I don't let any toxic drug to pass my lips and that also would include LDN. Gill (UK) rich perillo wrote: > > All very impressive retoric, but I do'nt see anything in referance to Toxins " the cause " , or nutrients " to repair " is never there. It's the same with cancer research for the past 60 years, we're so close, all we need is more money, and nothing changes. We're made out of nutrients but thats not what they [research]. Can't patent nutrients. No big profits.........RP Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2007 Report Share Posted July 2, 2007 Hi Gill, I take LDN. What proof do you have that it is toxic? Regards, Dudley Delany http://profiles.yahoo.com/dudley_delany Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2007 Report Share Posted July 2, 2007 Hi Rich, Do you have proof that LDN is toxic? Regards, Dudley Delany http://profiles.yahoo.com/dudley_delany Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2007 Report Share Posted July 2, 2007 And I agree with you Gill, for the most part, regarding drugs. But I would recommend LDN in " low dose " if it is helpfull. ....RP Gill Butts wrote: Well said! There are so many people just waiting for miracle cures from toxic drugs when the answer is to give your body the nutrition it needs and in time it will heal itself!! I don't let any toxic drug to pass my lips and that also would include LDN. Gill (UK) rich perillo wrote: > > All very impressive retoric, but I do'nt see anything in referance to Toxins " the cause " , or nutrients " to repair " is never there. It's the same with cancer research for the past 60 years, we're so close, all we need is more money, and nothing changes. We're made out of nutrients but thats not what they [research]. Can't patent nutrients. No big profits.........RP --------------------------------- Looking for earth-friendly autos? Browse Top Cars by " Green Rating " at Yahoo! Autos' Green Center. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2007 Report Share Posted July 2, 2007 Hi Nina, LDN stands for " Low Dose Naltrexone. " For more information about LDN, visit http://tinyurl.com/2boot2 All the best, Dudley Delany http://profiles.yahoo.com/dudley_delany Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2007 Report Share Posted July 2, 2007 Good morning Dudley, I do'nt have any proof myself, but the manufacturer of Naltrexone warns, do not take it if you have liver disease, and it can cause vomiting, joint,muscle and stomach pain, nausea, fatigue, nervousness, headach and so on. But the normal dose I believe is 150mg for a different condition. I am not opposed to 'low dose'. ....RP DudleyDelany@... wrote: Hi Rich, Do you have proof that LDN is toxic? Regards, Dudley Delany http://profiles.yahoo.com/dudley_delany --------------------------------- Get the free Yahoo! toolbar and rest assured with the added security of spyware protection. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2007 Report Share Posted July 2, 2007 Thanks, very much, Dudley! :-) Nina DudleyDelany@... wrote: Hi Nina, LDN stands for " Low Dose Naltrexone. " For more information about LDN, visit http://tinyurl.com/2boot2 All the best, Dudley Delany http://profiles.yahoo.com/dudley_delany --------------------------------- Get your own web address. Have a HUGE year through Yahoo! Small Business. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2007 Report Share Posted July 2, 2007 Hi Rich, The normal dose of Naltrexone is 50 mg daily. It is the dose considered " safe " by the FDA. The dose recommended for MS is less than one tenth of that and is generally considered nontoxic. Dudley Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2007 Report Share Posted July 2, 2007 You're very welcome, Nina. Glad to be of service! Dudley http://profiles.yahoo.com/dudley_delany Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2007 Report Share Posted July 2, 2007 Thank you Dudley, the normal dose is 50mg a day. The PDR says you can take 150mg every three days if you wish. That is NOT the dose for M/S you all. ....RP DudleyDelany@... wrote: Hi Rich, The normal dose of Naltrexone is 50 mg daily. It is the dose considered " safe " by the FDA. The dose recommended for MS is less than one tenth of that and is generally considered nontoxic. Dudley --------------------------------- Got a little couch potato? Check out fun summer activities for kids. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 2, 2007 Report Share Posted July 2, 2007 Thanks for this information. I hope there continues to be studies of how to live with or how to cure MS and I appreciate reading of these studies. Whether I use any of these cures is my decision in the end but I am glad people are looking. MS Article A New Line Of Communication Between Nervous System Cells Discovered By Weizmann Scientists Main Category: Neurology / Neuroscience News Article Date: 30 Jun 2007 - 13:00 PDT In a host of neurological diseases, including multiple sclerosis (MS) and several neuropathies, the protective covering surrounding the nerves - an insulating material called myelin - is damaged. Scientists at the Weizmann Institute of Science have now discovered an important new line of communication between nervous system cells that is crucial to the development of myelinated nerves - a discovery that may aid in restoring the normal function of the affected nerve fibers. Nerve cells (neurons) have long, thin extensions called axons that can reach up to a meter and or more in length. Often, these extensions are covered by myelin, which is formed by a group of specialized cells called glia. Glial cells revolve around the axon, laying down the myelin sheath in segments, leaving small nodes of exposed nerve in between. More than just protection for the delicate axons, the myelin covering allows nerve signals to jump instantaneously between nodes, making the transfer of these signals quick and efficient. When myelin is missing or damaged, the nerve signals can't skip properly down the axons, leading to abnormal function of the affected nerve and often to its degeneration. In research published recently in Nature Neuroscience, Weizmann Institute scientists Prof. Elior Peles, graduate student Ivo Spiegel, and their colleagues in the Molecular Cell Biology Department and in the United States, have now provided a vital insight into the mechanism by which glial cells recognize and myelinate axons. How do the glial cells and the axon coordinate this process " The Weizmann Institute team found a pair of proteins that pass messages from axons to glial cells. These proteins, called Necl1 and Necl4, belong to a larger family of cell adhesion molecules, so called because they sit on the outer membranes of cells and help them to stick together. Peles and his team discovered that even when removed from their cells, Necl1, normally found on the axon surface, and Necl4, which is found on the glial cell membrane, adhere tightly together. When these molecules are in their natural places, they not only create physical contact between axon and glial cell, but also serve to transfer signals to the cell interior, initiating changes needed to undertake myelination. The scientists found that production of Necl4 in the glial cells rises when they come into close contact with an unmyelinated axon, and as the process of myelination begins. They observed that if Necl4 is absent in the glial cells, or if they blocked the attachment of Necl4 to Necl1, the axons that were contacted by glial cells did not myelinate. In the same time period, myelin wrapping was already well underway around most of the axons in the control group. " What we've discovered is a completely new means of communication between these nervous system cells, " says Peles. " The drugs now used to treat MS and other degenerative diseases in which myelin is affected can only slow the disease, but not stop or cure it. Today, we can't reverse the nerve damage caused by these disorders. But if we can understand the mechanisms that control the process of wrapping the axons by their protective sheath, we might be able to recreate that process in patients. " ### http://www.medicaln ewstoday. com/medicalnews. php?newsid= 75315 & nfid= rssfeeds <!-- #ygrp-mlmsg {font-size:13px;font-family:arial, helvetica, clean, sans-serif;} #ygrp-mlmsg table {font-size:inherit;font:100%;} #ygrp-mlmsg select, input, textarea {font:99% arial, helvetica, clean, sans-serif;} #ygrp-mlmsg pre, code {font:115% monospace;} #ygrp-mlmsg * {line-height:1.22em;} #ygrp-text{ font-family:Georgia; } #ygrp-text p{ margin:0 0 1em 0;} #ygrp-tpmsgs{ font-family:Arial; clear:both;} #ygrp-vitnav{ padding-top:10px;font-family:Verdana;font-size:77%;margin:0;} #ygrp-vitnav a{ padding:0 1px;} #ygrp-actbar{ clear:both;margin:25px 0;white-space:nowrap;color:#666;text-align:right;} #ygrp-actbar .left{ float:left;white-space:nowrap;} ..bld{font-weight:bold;} #ygrp-grft{ font-family:Verdana;font-size:77%;padding:15px 0;} #ygrp-ft{ font-family:verdana;font-size:77%;border-top:1px solid #666; padding:5px 0; } #ygrp-mlmsg #logo{ padding-bottom:10px;} #ygrp-vital{ background-color:#e0ecee;margin-bottom:20px;padding:2px 0 8px 8px;} #ygrp-vital #vithd{ font-size:77%;font-family:Verdana;font-weight:bold;color:#333;text-transform:upp\ ercase;} #ygrp-vital ul{ padding:0;margin:2px 0;} #ygrp-vital ul li{ list-style-type:none;clear:both;border:1px solid #e0ecee; } #ygrp-vital ul li .ct{ font-weight:bold;color:#ff7900;float:right;width:2em;text-align:right;padding-ri\ ght:.5em;} #ygrp-vital ul li .cat{ font-weight:bold;} #ygrp-vital a { text-decoration:none;} #ygrp-vital a:hover{ text-decoration:underline;} #ygrp-sponsor #hd{ color:#999;font-size:77%;} #ygrp-sponsor #ov{ padding:6px 13px;background-color:#e0ecee;margin-bottom:20px;} #ygrp-sponsor #ov ul{ padding:0 0 0 8px;margin:0;} #ygrp-sponsor #ov li{ list-style-type:square;padding:6px 0;font-size:77%;} #ygrp-sponsor #ov li a{ text-decoration:none;font-size:130%;} #ygrp-sponsor #nc { background-color:#eee;margin-bottom:20px;padding:0 8px;} #ygrp-sponsor .ad{ padding:8px 0;} #ygrp-sponsor .ad #hd1{ font-family:Arial;font-weight:bold;color:#628c2a;font-size:100%;line-height:122%\ ;} #ygrp-sponsor .ad a{ text-decoration:none;} #ygrp-sponsor .ad a:hover{ text-decoration:underline;} #ygrp-sponsor .ad p{ margin:0;} o {font-size:0;} ..MsoNormal { margin:0 0 0 0;} #ygrp-text tt{ font-size:120%;} blockquote{margin:0 0 0 4px;} ..replbq {margin:4;} --> ________________________________________________________________________________\ ____ Yahoo!7 Mail has just got even bigger and better with unlimited storage on all webmail accounts. http://au.docs.yahoo.com/mail/unlimitedstorage.html Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 3, 2007 Report Share Posted July 3, 2007 My understanding is that any medication is not natural and not good for the liver. However, in dealing with MS, one must weigh the risks and benefits of various treatments. I would prefer to be on no meds, but I do take LDN to help control the disease progression. If I ever feel I have cured my MS, I will stop the LDN. > > Good morning Dudley, I do'nt have any proof myself, but the manufacturer of Naltrexone warns, do not take it if you have liver disease, and it can cause vomiting, joint,muscle and stomach pain, Quote Link to comment Share on other sites More sharing options...
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