Jump to content
  • 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

Monosodium Glutamate And Celiac Disease


NEURO

Recommended Posts

NEURO Newbie

I have been reading some of the old posts about msg and that it is specifically gluten free (unless it is from a wheat source). The research that I have done shows that it is a free form of glutamic acid. I was curious if this extra source of glutamic acid might aid the transglutaminase (tTG) in changing the glutamines at positions p1 and p9 in the HLA-DQ2 and HLA-DQ8 molecules to glutamic acid (due to abundence of glutamic acid or change in pH levels of of the surroundings) causing the T-cell respond to the incorrect sequence in the molecules. Can the presence of the extra glutamic acid trigger a response from the immune system due to sensitivity to the similarity in the change of gluten by tTG?


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



Celiac.com Sponsor (A8-M):



larry mac Enthusiast
I have been reading some of the old posts about msg and that it is specifically gluten free (unless it is from a wheat source). The research that I have done shows that it is a free form of glutamic acid. I was curious if this extra source of glutamic acid might aid the transglutaminase (tTG) in changing the glutamines at positions p1 and p9 in the HLA-DQ2 and HLA-DQ8 molecules to glutamic acid (due to abundence of glutamic acid or change in pH levels of of the surroundings) causing the T-cell respond to the incorrect sequence in the molecules. Can the presence of the extra glutamic acid trigger a response from the immune system due to sensitivity to the similarity in the change of gluten by tTG?

Are you proposing that MSG may mimic gluten intolerance, or add to it? I don't profess to understand all the chemistry, but that sounds pretty far-fetched to me, especially any PH effect. I'm guessing that doctors & researchers would have seen that connection right off. But, who knows, you could win a Nobel prize or something! A quick trip to Open Original Shared Link reveals several interesting aspects of Glutamate & Glutamine ( I take 4.5g daily as a powdered supplement ). BTW, as far as I know, I personally have never had a problem with MSG, so have never paid much attention to it. Please refer to the link for a listing of naturally occurring glutamate levels in food. This is good info I would recommend to everyone.

"Many people believe that MSG Speeds up the digestion of healthy proteins.

As a result of consuming MSG or protein-based foods, a natural elevation of the blood glutamate level will occur. That level will return to "baseline" (or the level before eating) in about three hours, no matter what the source of glutamate.

Glutamine, and the closely-related compound glutamate, are two amino acids that are critical to human health. In humans, animals, and plants, glutamine and glutamate are transformed into each other as part of numerous physiological processes. The roles of these amino acids in human diseases were intensively researched during the past decade and continue to be the subject of scrutiny. One area of interest is their potential health effects when they are provided in addition to the normal dietary intake that is already several grams per day.

Glutamine has been recommended by nutritionists as a dietary supplement for several serious disease conditions and there is growing research support for this action. Hospital dietitians are aware of the value of administering glutamine in parenteral nutrition (IV nutrition) for critically ill patients, and especially for patients who have had intestinal surgery, but physicians rarely recommend glutamine supplementation in other situations for which it may be indicated. Therefore, it is valuable for other health care providers to be familiar with the over-the-counter availability and uses of glutamine for supplementation purposes."

and of special interest to the MSG sensitive:

"(in the United States) Under current FDA regulations, significant amounts of free glutamate can be included in food under the following ingredient labels: MSG, monosodium glutamate, glutamic acid, hydrolyzed protein, autolyzed protein, textured protein, yeast extract, autolyzed yeast extract, protein isolate, soy sauce, modified food starch, modified corn starch, calcium caseinate, and sodium caseinate. In some cases, significant amounts of free glutamate are also added as broth, maltodextrin, seasonings, or natural flavor."

Theres lots more, also click on the glutamic acid link. best regards, lm

maximumbob Newbie

2/5/07

In response to MSG and glutamates, etc., I need to know if "autolyzed (sic) yeast extract: listed in chicken broth, is potent to someone with celiac disease. I suspect it is used as falvoring, i.e. MSG.

My wife was diagnosed in '98 with celiac disease (blood test only), also lactose intolernace, and has lost about 30 pounds in the last three months (shortly after suspect TIA) but may have now stablized at about 106 lbs, dressed, at 5'4". Trying very hard to maintain strict diet and haven't been able to find out if small intestine has flatened villa and/or there is musous damage to wall, which I suspect is the cause for malabsorption. Will find out in a couple of days. Have her on probiotics, two types (Florastor), enzymes, vitamins, etc. She is very depressed but continues to work as OTR with autistic children. Buy from Whole Foods and bread from Celiac Free local restaruant/bakery that has a celiac disease free menu.

Can't find a local GI speacialist or someone locally that knows what they are doing in this area. I guess I need to find a local celiac disease support group.

Tired of printing up list that are all suspect because of changing contents or discoveries that things are now suspect, or or no longer suspect.

Does any one know how the phase two tests is coming along in Palo Alto, Calif. I am sorry but I don't have the specific info as I am work, but it was the company that got a 21 mil grant to proceed with its specicifc molecule testing.

Sorry for covering to many areas.yeast

I do have a toll free number, but being new to this site, not sure that I can provide it.

Any info is appreciated,

Maximumbob

amarieski Apprentice
2/5/07

In response to MSG and glutamates, etc., I need to know if "autolyzed (sic) yeast extract: listed in chicken broth, is potent to someone with celiac disease. I suspect it is used as falvoring, i.e. MSG.

My wife was diagnosed in '98 with celiac disease (blood test only), also lactose intolernace, and has lost about 30 pounds in the last three months (shortly after suspect TIA) but may have now stablized at about 106 lbs, dressed, at 5'4". Trying very hard to maintain strict diet and haven't been able to find out if small intestine has flatened villa and/or there is musous damage to wall, which I suspect is the cause for malabsorption. Will find out in a couple of days. Have her on probiotics, two types (Florastor), enzymes, vitamins, etc. She is very depressed but continues to work as OTR with autistic children. Buy from Whole Foods and bread from Celiac Free local restaruant/bakery that has a celiac disease free menu.

Can't find a local GI speacialist or someone locally that knows what they are doing in this area. I guess I need to find a local celiac disease support group.

Tired of printing up list that are all suspect because of changing contents or discoveries that things are now suspect, or or no longer suspect.

Does any one know how the phase two tests is coming along in Palo Alto, Calif. I am sorry but I don't have the specific info as I am work, but it was the company that got a 21 mil grant to proceed with its specicifc molecule testing.

Sorry for covering to many areas.yeast

I do have a toll free number, but being new to this site, not sure that I can provide it.

Any info is appreciated,

Maximumbob

I know before I was diagnosed with celiac I was told to avoid all msg for reactions, example: chinese food because I felt so terrible after I ate it, neck pain, light headed heart palps and severe fatigue and of course other minor things but now I wonder if it was the celiac? but otherwise there is a list of symptoms in reaction to forms of msg here is that site............. Open Original Shared Link and here is a way to identify hidden types of msg in food labels .......... Open Original Shared Link and here is last but not least the answer to your question, states here that it is a primary source for msg. I hope this helps Open Original Shared Link. and this site but you have to read through it I know its on this page says it may be intolerant for celiacs, I guess be safe than sorry? Open Original Shared Link

tummytroubles Newbie

All I know is that I very much react to MSG. It actually gives me symptoms similar to a mild multiple sclerosis flare up. I don't know if I react because it is related to the whole gluten intolerance thing, or if it because of my MS though.

UR Groovy Explorer
All I know is that I very much react to MSG. It actually gives me symptoms similar to a mild multiple sclerosis flare up. I don't know if I react because it is related to the whole gluten intolerance thing, or if it because of my MS though.

To all you MSG problematic people:

Beware of Tomato juice or over-ripe tomatoes

bluejeangirl Contributor
To all you MSG problematic people:

Beware of Tomato juice or over-ripe tomatoes


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



Celiac.com Sponsor (A8-M):



UR Groovy Explorer

--

  • 5 months later...
GFAngel Newbie

I just wanted to add what I'd recently transcribed from a tv health show I watch. I'm very confused about gluten being in MSG - I've read it is and it isn't. Either way, it doesn't sound very healthy. I thought anyone reading about MSG might be able to use this to further their research:

Your Health with Dr. Richard and Cindy Becker (viewed on KSBI-TV Ch. 52, OKC on Tuesday, July 10, 2007)

Today

Archived

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

  • Get Celiac.com Updates:
    Support Celiac.com:
    Join eNewsletter
    Donate

  • Celiac.com Sponsor (A17):
    Celiac.com Sponsor (A17):





    Celiac.com Sponsors (A17-M):




  • Recent Activity

    1. - trents replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      7

      Help understand results

    2. - Jordan Carlson posted a topic in Post Diagnosis, Recovery & Treatment of Celiac Disease
      0

      Fruits & Veggies

    3. - wellthatsfun posted a topic in Gluten-Free Recipes & Cooking Tips
      0

      heaps of hope!

    4. - Tanisha L commented on Scott Adams's article in Kids and Celiac Disease
      1

      New Study Reveals Age and Racial Gaps in Pediatric Celiac Testing

    5. - knitty kitty replied to mamaof7's topic in Parents, Friends and Loved Ones of Celiacs
      7

      Help understand results

  • Celiac.com Sponsor (A19):
  • Member Statistics

    • Total Members
      132,997
    • Most Online (within 30 mins)
      7,748

    IwannabHealthy
    Newest Member
    IwannabHealthy
    Joined
  • Celiac.com Sponsor (A20):
  • Celiac.com Sponsor (A22):
  • Forum Statistics

    • Total Topics
      121.5k
    • Total Posts
      1m
  • Celiac.com Sponsor (A21):
  • Upcoming Events

  • Posts

    • trents
      Actually, it would be more correct to say that the genetic potential to develop celiac disease is passed down from parents to children. About 40% of the general population has the genetic potential to develop celiac disease but only about 1% of the general population actually do. But it is also true that the offspring of those who do have active celiac disease are at a considerably higher risk of developing active celiac disease than those of parents who have the genes but don't develop the disease. Some recent, larger studies put the risk at near 50% for the first degree relatives of those who have active celiac disease.
    • Jordan Carlson
      Hello everyone! Been a while since I posted. The past few moths have been the best by for recovery for myself. I have been the least bloated I have ever been, my constant throat clearing is almost gone, I have stopped almost all medication I was prevously taking (was taking vyvanse for adhd, pristiq for anxiety,fomotadine/blexten for histamine blockers and singulair). Only thing I take now is Tecta. I also no longer get any rashes after eating. Things are going very well. Most success came actually once I upped my B12 daily dose to 5,000 mcg. I do have one thing I am un able to figure out and want to see if anyone else has this issue or has experience working around it. Ever since I was born I have always had a issue getting fruits and veggies down. No matter how hard I tried, it would always result in gagging or throwing up. Always just thought I was a picky eater. Now that my stomach and system has healed enough that I can feel when something is off almost istantly, I notice that after eating most fruits (sometimes I am ok with bananas) and veggies, my stomach instantly starts burning and my heart starts to pound and I get really anxious as if my body doesnt know what to do with what just enetered it. So I am thinking now that this is what probably was going on when I was born and my body started rejecting it before which caused this weird sensory issue with it causing the gagging. Hoping someone has some exprience with this as well because I would love to be able to enjoy a nice fruit smoothie once in a while haha. Thanks everyone!
    • wellthatsfun
      i know i've been rather cynical and sad about being fully diagnosed in june 2025, but my boyfriend has been consistently showing me the wonderful world that is gluten free cooking and baking. in the past couple of days he's made me a gluten free rice paper-wrapped spanakopita "pastry", plus a wonderful mac and cheese bechamel-ish sauce with gluten free pasta (san remo brand if you're in australia/if you can get your hands on it wherever you are).  those meals are notably gluten free, but mainly he's been making me easy gluten free meals - chili mince with white rice and sour cream, chicken soup with homemade stock from the chicken remains, and roast chickens with rice flour gravy and roast veggies. i'm a bit too thankful and grateful lol. how lucky could i possibly be? and, of course, for those who don't have someone to cook for them, it's quite easy to learn to cook for yourself. i've been making a lot of meals for us too. honestly, cooking is pretty darn fun! knowing basic knife skills and sanitary practices are all you really need. experimenting with spices will help you get on track to creating some really flavourful and yummy dishes. coeliac is a pain, but you can use it to your advantage. healthier eating and having fun in the kitchen are major upsides. much luck to all of you! let's be healthy!
    • knitty kitty
      That test is saying that your daughter is not making normal amounts of any IGA antibodies.  She's not making normal amounts of antibodies against gliadin, not against bacteria, not against viruses.  She is deficient in total IGA, so the test for antigliadin antibodies is not valid.  The test was a failure.  The test only works if all different kinds of antibodies were being made.  Your daughter is not making all different kinds of antibodies, so the test results are moot.  Your daughter should have the DGP IgG and TTG IgG tests done.   The tests should be performed while she is still consuming gluten.  Stopping and restarting a gluten containing diet can make her more sick, just like you refuse to eat gluten for testing.  Call the doctor's office, request both the IGG tests. Request to be put on the cancellation list for an appointment sooner.  Ask for genetic testing.   Celiac disease is passed on from parents to children.  You and all seven children should be tested for genes for Celiac disease.  Your parents, your siblings and their children should be tested as well.  Eating gluten is not required for genetic testing because your genes don't change.  Genetic testing is not a diagnosis of Celiac disease.  Just having the genes means there is the potential of developing Celiac disease if the Celiac genes are activated.  Genetic testing helps us decide if the Celiac genes are activated when coupled with physical symptoms, antibody testing, and biopsy examination. It's frustrating when doctors get it wrong and we suffer for it.  Hang in there.  You're a good mom for pursuing this!  
    • knitty kitty
      @hjayne19, So glad you found the information helpful.  I know how difficult my struggle with anxiety has been.  I've been finding things that helped me and sharing that with others makes my journey worthwhile. I like Life Extension Bioactive Complete B Complex.  It contains the easily activated forms of B vitamins needed by people with the MTHFR genetic variation often found with Celiac disease.   Avoid B Complex vitamins if they contain Thiamine Mononitrate if possible.  (Read the ingredients listing.)  Thiamine Mononitrate is the "shelf-stable" form of B 1 that the body can't utilize.  B vitamins breakdown when exposed to heat and light, and over time.  So "shelf-stable" forms won't breakdown sitting on a shelf in a bright store waiting to be bought.  (It's also very cheap.)  Thiamine Mononitrate is so shelf-stable that the body only absorbs about thirty percent of it, and less than that is utilized.  It takes thiamine already in the body to turn Thiamine Mononitrate into an active form.   I take MegaBenfotiamine by Life Extension.  Benfotiamine has been shown to promote intestinal healing, neuropathy, brain function, glycemic control, and athletic performance.   I take TTFD-B1 Max by Maxlife Naturals, Ecological Formulas Allthiamine (TTFD), or Thiamax by EO Nutrition.  Thiamine Tetrahydrofurfuryl Disulfide (TTFD for short) gets into the brain and makes a huge difference with the anxiety and getting the brain off the hamster wheel.  Especially when taken with Magnesium Threonate.   Any form of Thiamine needs Magnesium to make life sustaining enzymes and energy.  I like NeuroMag by Life Extension.  It contains Magnesium Threonate, a form of magnesium that easily crosses the blood brain barrier.  My brain felt like it gave a huge sigh of relief and relaxed when I started taking this and still makes a difference daily.   Other brands of supplements i like are Now Foods, Amazing Formulas, Doctor's Best, Nature's Way, Best Naturals, Thorne, EO Nutrition. Naturewise.  But I do read the ingredients labels all the time just to be sure they are gluten and dairy free. Glad to help with further questions.  
×
×
  • Create New...

Important Information

NOTICE: This site places This site places cookies on your device (Cookie settings). on your device. Continued use is acceptance of our Terms of Use, and Privacy Policy.