Jump to content
This site uses cookies. Continued use is acceptance of our Terms of Use and Privacy Policy. More Info... ×
  • Welcome to Celiac.com!

    You have found your celiac tribe! Join us and ask questions in our forum, share your story, and connect with others.




  • Celiac.com Sponsor (A1):



    Celiac.com Sponsor (A1-M):


  • Get Celiac.com Updates:
    Support Our Content
    eNewsletter
    Donate

Glutamine For Intestinal Healing


Lizz7711

Recommended Posts

Lizz7711 Apprentice

On another thread we were discussing the issue of taking l-glutamine for intestinal healing. I have my concerns based on the body's ability to convert glutamine to free glutamic acid if there is already enough glutamine in the system, then it crosses the blood/brain barrier and can do damage. But, maybe taking glutamine in this form is safe. Does anyone have any experience with this amino acid? Any positive results or negative effects?

thanks!

Here's what I posted on the other thread (I don't know how to put the link on here so I just copied and pasted!):

Basically, glutamine is the same as glutamic acid...just different forms of the same amino acid. glutamine, or glutamic acid is naturally present in many foods, mostly meat, dairy...and when it is bound to proteins, it is largely harmless, although I think you can still get too much..for instance, parmesan cheese is way high in glutamic acid and my daughter reacts to it like MSG. But when it is separated from proteins, as in the case of MSG, isolated soy protein etc, it becomes an excitotoxin in our brains. To make a supplement called glutamine, they MUST be separating it from it's natural protein buddies found in food, so this is why i'm very worried about taking it. There's a great book written by Russell Blaylock called "Excitotoxins: the taste that kills"--he's a neurosurgeon and is very worried about these compounds, especially glutamate and aspartate.

Anyway, here is some info from wikipedia, this talks about the role of glutamate as a neurotransmitter and how, while it can be beneficial, TOO MUCH can cause it to cross the blood/brain barrier.

Open Original Shared Link

Glutamic acid (abbreviated as Glu or E; the abbreviation Glx or Z represents either glutamic acid or glutamine). The carboxylate anion of glutamic acid is known as glutamate, and this is one of the 20 proteinogenic amino acids. It is not among the human essential amino acids.

Glutamate transporters[3] are found in neuronal and glial membranes. They rapidly remove glutamate from the extracellular space. In brain injury or disease, they can work in reverse and excess glutamate can accumulate outside cells. This process causes calcium ions to enter cells via NMDA receptor channels, leading to neuronal damage and eventual cell death, and is called excitotoxicity. The mechanisms of cell death include

Damage to mitochondria from excessively high intracellular Ca2+;[4]

Glu/Ca2+-mediated promotion of transcription factors for pro-apoptotic genes, or downregulation of transcription factors for anti-apoptotic genes.

Excitotoxicity due to glutamate occurs as part of the ischemic cascade and is associated with stroke and diseases like amyotrophic lateral sclerosis, lathyrism, autism, some forms of mental retardation and Alzheimer's disease.

Glutamic acid has been implicated in epileptic seizures. Microinjection of glutamic acid into neurons produces spontaneous depolarisations around one second apart, and this firing pattern is similar to what is known as paroxysmal depolarizing shift in epileptic attacks. This change in the resting membrane potential at seizure foci could cause spontaneous opening of voltage-activated calcium channels, leading to glutamic acid release and further depolarization.

________________________

Here's another site about glutamine: Open Original Shared Link

It sounds like it may possibly be safe to take it if you're sure you don't already have brain damage. Thjat's the tricky part...how do we know what the accumulation of glutamine is in our system? My dad's mom had alzheimer's and they say for people with alzheimer's to NOT take it, so I think i'll not let my dad try it. But I myself might at least try it, guess that's the only way to know what it's effect is eh?


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Cinnamon Apprentice

I tried giving it to my son awhile back, and he reacted badly to it. I'd read so many good things about it being so helpful for intestinal healing, and hadn't made the association between glutamine and glutamate, but I think you are right. If a person is sensitive to MSG, they shouldn't try it. If a person has any neurological symptoms, they shouldn't try it. But for someone who only has intestinal issues and can tolerate MSG, it might be fine. I could probablyuse it since none of that stuff bothers me at all. I used to drink Diet Coke by the gallon, and MSG is no problem. But some people are really sensitive, like my son. And all you hear when you research glutamine is how great it is, so it's good to put this out there. It isn't good for everyone.

Cinnamon Apprentice

Oh, just to clarify, my son has neurological symptoms of celiac. He had been having what appeared to be partial seizures, though we don't know for sure since he never had one during an EEG. He had ataxia symptoms, brain fog, rashes, but didn't have the traditional digestive symptoms, so he's not the textbook celiac type.

RiceGuy Collaborator

I agree that L-Glutamine could cross the blood-brain barrier. What I have yet to verify is if the supplements have a form which is bound up in another molecule. I'm guessing not, and L-Glutamine is the kind of glutamic acid which makes MSG do what it does.

Even if a person doesn't have any noticeable negative reaction to it, how would one be certain that there isn't any damage being done? After all, even with Celiac, many people are asymptomatic.

Lizz7711 Apprentice

I've been re-reading portions of the book "Excitotoxins: the Taste that Kills" by Russell Blaylock, MD and it seems clear from his studies as a neurosurgeon, that high levels of glutamine/glutamate or aspartate are damaging to EVERYONE, even if not noticable, but especially to those with neurological/degenerative diseases or brain damage. So I think it's good that you realized how bad it is for your son. But I also think you should avoid it as much as possible for yourself...some damage is unfelt and unseen until all of a sudden a person gets something like Alzheimer's ya know?

I think it isn't good for anyone. :)

thanks for your comments!

I tried giving it to my son awhile back, and he reacted badly to it. I'd read so many good things about it being so helpful for intestinal healing, and hadn't made the association between glutamine and glutamate, but I think you are right. If a person is sensitive to MSG, they shouldn't try it. If a person has any neurological symptoms, they shouldn't try it. But for someone who only has intestinal issues and can tolerate MSG, it might be fine. I could probablyuse it since none of that stuff bothers me at all. I used to drink Diet Coke by the gallon, and MSG is no problem. But some people are really sensitive, like my son. And all you hear when you research glutamine is how great it is, so it's good to put this out there. It isn't good for everyone.
Lizz7711 Apprentice
I agree that L-Glutamine could cross the blood-brain barrier. What I have yet to verify is if the supplements have a form which is bound up in another molecule. I'm guessing not, and L-Glutamine is the kind of glutamic acid which makes MSG do what it does.

Even if a person doesn't have any noticeable negative reaction to it, how would one be certain that there isn't any damage being done? After all, even with Celiac, many people are asymptomatic.

I think even if the glutamine was bound with another molecule, it would still be dangerous esp. for those already sensitive to MSG etc. Although we do eat many foods that have glutamine in them and it is not inherently bad for us, it seems that many people get too much from many sources and once it reaches a certain threshold, accumulates outside the brain and then crosses the blood/brain barrier.

Here is an excerpt from the book "Excitotoxins: The Taste that Kills" by Russell Blaylock, MD p. 204, 208-209. It's taken from a section where he is talking about strokes.

"The pathological findings seen with strokes closely resemble the selective neuron damage observed with excitotoxins. I have tried to demonstrate that excitotoxins, especially glutamate and aspartate, play a major role in strokes and conditions in which oxygen is in short supply. This excitotoxin accumulation is secondary to release withing the brain itself and not due to that taken in the diet. But, knowing that the blood-brain barrier is damaged by strokes and during hypoxia, one logically must assume that high levels of dietary excitotoxins can pose a significatnt threat to ther survival of these floundering neurons in the penumbra zone. In addition , we know that some people are unable to metabolize glutamate from their diet, resulting in abnormal, toxic accumulations in the blood, and hence, within the injured brain. At present we have no inexpenseive way to determine who these unfortunate people are.

We have seen that our normal diet contains enormous amounts of excitotoxins in various forms. Those in liquid form, such as NutraSweet sweetened beverages and MSG containing soups, are more rapidly completely absorbed and therefore pose the greatest risk. Some hospitals add these excitotoxin food additives to the patient's food. In fact, several nutritionists are recommending that glutamine (the precursor of glutamate) be added to the diet of seriously ill patients to improve intestinal function. And cardiologists in some medical centers hae concocted a cocktail containing high concentrations of MSG, with the idea that the glutamate will imporve cardiac function. Patinets on the heart pump frequently have multiple micro-strokes, which would make them very susceptible to occult brain damage. In my opinion, this practice should be stopped".

It is clear from the rest of the book, that glutamate and aspartate are excitotoxins that damage neurons in all people, and so should be avoided even if you don't notice any effects, as you said RiceGuy--it can be silent damage just like silent celiac disease!

My big question now is this: to me it seems that the reason some people like myself and my daughter, have multiple chemical sensitivities and react to MSG and aspartame, must be that there is damage to the blood-brain barrier and more molecules are crossing than they are in other people. Initiailly I was thinking this was due to leaky gut. But when I inhale chemicals...it's not going through my intestine and into the blood stream but through my lungs and into the blood stream. So the common point, is that they are crossing the BLOOD-BRAIN BARRIER and causing distress (headaches, mood changes, rage attacks etc) same thing with gluten. So while I can work on fixing the leaky gut to lower it happening so rapidly from foods, how do I heal the blood-brain barrier leak???

Any thoughts on that? lol :)

Cinnamon Apprentice

Yes, good point. Just because there are no symptoms doesn't mean damage isn't being done. And even though glutamine is naturally occurring in common foods doesn't mean it's safe to super-concentrate it and take large megadoses, especially since it enters the brain. Best to stay away from it. There are other healing supplements out there. We liked Slippery Elm.


Celiac.com Sponsor (A8):
Celiac.com Sponsor (A8):



Celiac.com Sponsor (A8-M):



Lizz7711 Apprentice
Yes, good point. Just because there are no symptoms doesn't mean damage isn't being done. And even though glutamine is naturally occurring in common foods doesn't mean it's safe to super-concentrate it and take large megadoses, especially since it enters the brain. Best to stay away from it. There are other healing supplements out there. We liked Slippery Elm.

For anyone who reads through the other thread on L-glutamine...take a read of this one as well. In the other thread (from 2005), they discount Dr. Russell Blaylock's research on l-glutamine. Let me just say that this guy is a NEUROSURGEON. And he has over 500 scientific references in his book "Excitotoxins". I"m not saying he can't be wrong on occasioin...but this is something he has spent his life studying and I think i'd trust his view a little more than Dr. Mercola on this point.

I'm not saying it is for sure bad for everyone...but for those with any neurological involvemnet, leaky BBB, I personally would recommend caution/avoidance.

Archived

This topic is now archived and is closed to further replies.


  • Celiac.com Sponsor (A19):



  • Member Statistics

    • Total Members
      126,091
    • Most Online (within 30 mins)
      7,748

    Order Codeine Online Chris
    Newest Member
    Order Codeine Online Chris
    Joined

  • Celiac.com Sponsor (A20):


  • Forum Statistics

    • Total Topics
      120.9k
    • Total Posts
      69.2k

  • Celiac.com Sponsor (A22):





  • Celiac.com Sponsor (A21):



  • Upcoming Events

  • Posts

    • Kathleen JJ
      @cristiana Do you have any suggestions for the gummy bear type of candy? Because that is what is getting passed around. Someone told me "you will have to read all labels thoroughly from now on" but to be honest: I don't know what I'm looking for that should or should not be there? And is the notion "gluten free" trustable? And what about "may contain residual gluten"? Is that safe?
    • Kathleen JJ
      @trents The first thought indeed I had was 'thank god it's not cancer' and of course, there are many, many, many worse diagnoses to get. But this doesn't mean it doesn't come as a shock. I read a lot of the time 'the most common symptoms are...' and then all the things he doesn't have, but never do I find a list of less common symptoms (bar @Wheatwackeds examples - and also non of these are present). I get that severe pains can be a symptom, though the fact that they were omnipresent for 10 days (the exact time his viral values were up) and then 6 weeks later 1 episode also when the family was going through a stomach bug, and since then (nor ever before) none, this logically seems more related to a virus then a symptom of Coeliac, as I'd think this would have to be more present on a regular basis? He always has loved gluten-containing food and at that time was rather having less of it (due to the bug and feeling a little under the weather so eating more yoghurt and the likes then cookies) then more of it. It just doesn't sound all that logical. That being said, I comprehend AND accept that things can not always be logical.   I am trying to understand what you are saying about the tolerance - so as long as he eats gluten, he will have some tolerance to it, but when he stops, and say accidentally ingests something, he will react more as the tolerance is lower? It sounds so illogical (hmm, I see a pattern with myself: really looking for logic in a very illogical condition). And how do you interpret the values very 6 months as you maybe don't know there has been an accidental intake?  Do the values ever go down to zero or is it a question of getting them mainly lower and can they never go down to normal rates?   Normally results of his biopsy are coming in on monday, a little chance they come in today. I've been checking my mail every 10 seconds 🤦🏻‍♀️, this will not be a productive working day I fear 🙄. Then we know the values, but we only have an appointment with the specialized pediatrician and dietitian on December 6d (which in Belgium is a children's holiday comparable to Santa Clause). So we'll get the full "introduction" to the disorder and approach then.   I did talk to the pediatrician and gastrointestinal doctor who did the gastroscopy asking their advice about a plan I was having: to wait to start the diet after the holiday season, we will be abroad in a hotel and to start there in this very new world feels quite stressful for us, but even worse: it will start this journey in a lot of negativity. So our plan is to have a "yummy" party after we return from our trip, during Christmas holidays, inviting some of his friends and buying and making a vast array of gluten free goodies and having them sample and score it. This way it feels like a festive thing AND we can immediately find some things (hopefully) he genuinely like.   Both doctors agreed with this approach as this was truly an accidental find and hadn't we tested his blood 2 weeks ago chances were we'd only have found out in a year or 2 so those extra few weeks will not make the difference.   So now I'm gathering information, talking to people to know where there's good stuff...     But what keeps on being quite ununderstandable to me (I hope this will get explained on December 6th) is how it works. So it's auto-immune, meaning gluten trigger an immune response. Is this a black and white thing? Does 1 grain of wheat trigger the same response as a full bowl of spaghetti? And I mean this on a bowel and organs level, not on a symptoms level, as I gather (is this correct?) that not having any symptoms does not mean that his bowel doesn't get attacked?   I know it all could be worse, I truly do, but to be honest, this is the 4th "anvil falling on my head out of a clear blue sky" diagnosis that I got for one of my most loved people. First my mother was diagnosed with presenile dementia without anyone in the family having it. Then my unborn daughter turned out to have a chromosomal defect that made that she could only live inside of me and died when she was born, then my sister turned out to have (a tested non genetic 🤯) form of presenile dementia as well, with me being her only caretaker as my mother passed away a few years ago and she has no family of her own. And now this. And this is absolutely not only the least of this row but of course not even in the same ball park. But for my resilience and bearing capacity this just feels not little as it affects the life of my little boy...    
    • Wheatwacked
      Could be the Ozampic is masking your expected symptoms.  Like an analgesic masks pain.  Qzampic slows digestion to lower the rate glucose enters the intestine to slow its effect on glucose level.  It seems it might also slow down the gluten entry into the intestine, reducing its trigger level for the antibodies.  Ultimately the damage from gluten is the same, just not as fast so the pain is less.  Sourdough bread has less gluten.  Ozampic siows its entry.
    • Wheatwacked
      You can sell it better if the whole family does gluten free.  If he does have Celiac Diease, it is genetic so either you, your spouse, or both have a 40% chance of also having Celiac.  There are over 200 non classic symptoms also caused by celiac disease not often considered by doctors. Joint pain, muscle pain, muscle cramps, osteoporosis, and allergies for starters.  
    • Wheatwacked
      Hello @MHavoc, thank you for your question and welcome to the clinic. First, has the contstipation abated with the GFD? If your are pursuing further diagnostics you must continue to eat gluten. Each lab has their own reference range for their test, but they indicate an H for high.  Typically anything above 11 is considered positive. Mild chronic inflammation (gastritis) can interfere with intrinsic factor for B12 leading to low B12 causing low MCHC (anemia). So what is causing your gastritis?  A high tTG IgA level generally indicates potential gastrointestinal problems most commonly associated with celiac disease.  Although the biopsy is the Gold Standard for diagnosis, not finding damage in the biopsy does not rule out Celiac Disease. It means they did not find damage where they looked.  The small intestine is over 20 feet long. Many here have been blood positive and biopsy negative, it just delays the diagnosis until you have enough damage to find and fit their diagnostic profile. The Ttg-iga is not only sensitive (90%) but highly specific (98%) and won’t show positive until the damage is severe.  It is estimated that 40% of first degree relatives of diagnosed Celiacs have undiagnosed Celiac Disease, so your sister is a big risk factor in whether you have it. Are You Confused About Your Celiac Disease Lab Results?  This article explains it better and is quite readable. Celiac Disease can cause deficient vitamin D.  Low vitamin D compromises the immune system.  Any other symptoms? liver enzymes?  Recent cold or flue? Celiac Disease and the malabsorption it causes through vitamin and mineral deficiencies can elicit symptoms not usually associated with Celiac Disease. Case in point maybe your gastritis and anemia.  
×
×
  • Create New...