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    • sunsunsunS
      sunsunsun @LucH
      last edited by

      @LucH the lack of obvious BBB crossing apparently doesn't negate GABA effects , the basic reason I say that is that gut bacteria producing GABA have been measured to have distinct effect on whole organism

      jamezb46J LucHL 2 Replies Last reply Reply Quote 0
      • jamezb46J
        jamezb46 @sunsunsun
        last edited by

        @sunsunsun I think the trademarked pharmaGABA at least has some evidence behind it that shows it can exert parasympathetic action, possibly via the vagus nerve.

        https://pubmed.ncbi.nlm.nih.gov/30263304/

        https://pubmed.ncbi.nlm.nih.gov/16971751/
        https://www.tesble.com/10.1002/biof.5520260305

        The latter study found that 100 mg PharmaGABA produced better results than l-theanine (200mg) as regards alpha brain waves and beta brain waves, though both interventions produced favorable changes.

        GABA also prevented the decrease in Immunoglobulin A levels (a marker of immune suppression) when subjects were exposed to a stressor (walking a pedestrian bridge when they were afraid of heights) compared to placebo.

        In time there is life but no knowledge; outside time there is knowledge but no life

        sunsunsunS 1 Reply Last reply Reply Quote 1
        • sunsunsunS
          sunsunsun @jamezb46
          last edited by sunsunsun

          @jamezb46 apparently the pharmagaba is a psyop and normal synthetic gaba has the same effect. pharmagaba is produced by microbial fermentation which shouldn't change how the actual end-product works. a gaba researcher actually called them out on it in a submission to a journal or whatever. microbial fermentation to produce pharmaceuticals/supps is actually neat and i have nothing against it.

          jamezb46J 1 Reply Last reply Reply Quote 0
          • jamezb46J
            jamezb46 @sunsunsun
            last edited by

            @sunsunsun Perhaps, but it's possible that the GABA not produced by fermentation has unnatural ratios of the various conformations that GABA can exist in.

            In time there is life but no knowledge; outside time there is knowledge but no life

            LucHL sunsunsunS 2 Replies Last reply Reply Quote 1
            • LucHL
              LucH @jamezb46
              last edited by LucH

              @jamezb46 said in GABA powder:

              Perhaps, but it's possible that the GABA not produced by fermentation has unnatural ratios of the various conformations that GABA can exist in.

              I'd would express it on another way.
              Gut bacteria known to metabolize or grow on GABA
              A number of gut microbes possess the GABA shunt (gad/gab genes), allowing them to use GABA for growth, energy production, or acid resistance.

              Improve transit (MMC) to avoid most of the problems due to excess. No GABA supplement if suspicion of candidiasis.

              @sunsunsun
              I've just finished writing an article on why GABA powder is useful for the microbiota. Not yet posted. Need coffee 😉
              Thanks for contributing: I didn't know (...).

              1 Reply Last reply Reply Quote 1
              • sunsunsunS
                sunsunsun @jamezb46
                last edited by

                @jamezb46 Screenshot 2025-12-10 at 11.39.26 AM.png

                jamezb46J 1 Reply Last reply Reply Quote 0
                • jamezb46J
                  jamezb46 @sunsunsun
                  last edited by jamezb46

                  @sunsunsun

                  I would strongly advise against relying on Chat GPT to get your knowledge. It is frankly abysmal at chemistry. I have asked it specific questions that it gets completely wrong, referring in its answer to completely different molecules.

                  Here are some excerpts from the paper that my claim came from:

                  https://www.sciencedirect.com/science/article/pii/0166128088800848?via%3Dihub

                  "It is believed that the conformational behaviour of GABA and GABA inhibitors is a critical factor for their selective biological property. Experimental analysis on GABA, viz., X-ray crystallography [6-8], IR [9,10] and 1H-NMR spectroscopy [ 11 ], suggest that this amino acid exists mainly as a zwitterion in solid and gaseous state or in solution. Theoretical conformational analysis [12-16] of the isolated molecule predicted the lower energies for the folded conformer with a rotational barrier greater than 40 kcal mol- 1 for the extended conformer.

                  "Theoretical calculations involving solvent effects [ 13,15,17 ] have
                  shown that this rotational barrier is largely reduced in solution. Dipole moment measurements [18,19] favour the fully extended form whereas crystallographic evidence [6-8] supports a conformer which is not fully extended."

                  "Results of ~H-NMR measurements [11], on the other hand, predicted the existence of at least five extended and folded conformers in solution. The biological importance of the GABA conformation (i.e., the biologically active conformer) has been stressed by studies on the stereospecificity of GABA analogues [20-24]. For example, muscimol [25], a potent GABA agonist with respect to neuronal receptors, corresponds to a partially extended form of GABA
                  [24]. On the other hand, a wider range of conformers have been proposed to be the active forms at the perisynaptic uptake system [20,22,24 ]"

                  So, at least according to this paper, the particular effects that a particular GABA analogue has can be explained by whether the analogue resembles the extended or the folded conformation of GABA.

                  That implies that endogenously, there is a meaningful difference between the folded vs the extended form of GABA (if the authors are correct the folded vs extended forms have different affinities at GABA-A vs GABA-B receptors).

                  In time there is life but no knowledge; outside time there is knowledge but no life

                  sunsunsunS 1 Reply Last reply Reply Quote 1
                  • sunsunsunS
                    sunsunsun @jamezb46
                    last edited by

                    @jamezb46 said in GABA powder:

                    Here are some excerpts from the paper that my claim came from:

                    https://www.sciencedirect.com/science/article/pii/0166128088800848?via%3Dihub

                    "It is believed that the conformational behaviour of GABA and GABA inhibitors is a critical factor for their selective biological property. Experimental analysis on GABA, viz., X-ray crystallography [6-8], IR [9,10] and 1H-NMR spectroscopy [ 11 ], suggest that this amino acid exists mainly as a zwitterion in solid and gaseous state or in solution. Theoretical conformational analysis [12-16] of the isolated molecule predicted the lower energies for the folded conformer with a rotational barrier greater than 40 kcal mol- 1 for the extended conformer.

                    "Theoretical calculations involving solvent effects [ 13,15,17 ] have
                    shown that this rotational barrier is largely reduced in solution. Dipole moment measurements [18,19] favour the fully extended form whereas crystallographic evidence [6-8] supports a conformer which is not fully extended."

                    "Results of ~H-NMR measurements [11], on the other hand, predicted the existence of at least five extended and folded conformers in solution. The biological importance of the GABA conformation (i.e., the biologically active conformer) has been stressed by studies on the stereospecificity of GABA analogues [20-24]. For example, muscimol [25], a potent GABA agonist with respect to neuronal receptors, corresponds to a partially extended form of GABA
                    [24]. On the other hand, a wider range of conformers have been proposed to be the active forms at the perisynaptic uptake system [20,22,24 ]"

                    So, at least according to this paper, the particular effects that a particular GABA analogue has can be explained by whether the analogue resembles the extended or the folded conformation of GABA.

                    That implies that endogenously, there is a meaningful difference between the folded vs the extended form of GABA (if the authors are correct the folded vs extended forms have different affinities at GABA-A vs GABA-B receptors).

                    interdasting...

                    jamezb46J 1 Reply Last reply Reply Quote 0
                    • jamezb46J
                      jamezb46 @sunsunsun
                      last edited by jamezb46

                      @sunsunsun The paper could absolutely be wrong, or I could be misinterpreting it, but that was my impression, anyway.

                      In time there is life but no knowledge; outside time there is knowledge but no life

                      1 Reply Last reply Reply Quote 1
                      • LucHL
                        LucH @sunsunsun
                        last edited by

                        @sunsunsun said in GABA powder:

                        the lack of obvious BBB crossing apparently doesn't negate GABA effects , the basic reason I say that is that gut bacteria producing GABA have been measured to have distinct effect on whole organism

                        How is GABA powder useful for microbiota?
                        GABA → succinate → butyrate pathway: The Microbial Power Route.
                        How gut bacteria convert GABA through the shunt and succinate pathway to fuel and protect colonocytes of the linen walls.

                        Many Bacteroides can use GABA as a carbon and nitrogen source for growth. Some other intestinal bacteria can use an alternative pathway, called the GABA shunt.
                        GABA is not a preferred primary carbon source for most gut bacteria as growth is usually stronger on sugars or amino acids like glutamate. But when the main fuel is rationed or when an access route is blocked, an alternate pathway is used. Survival, no longer growing and extending.
                        Butyrate is the star among SCFAs (with propionate) as it upregulates the tight junction proteins (occludin, claudin-1 and -4and ZO-1 (zonulin): Tight junction expression, anti-inflammatory signaling (via HDAC inhibition) and hypoxic barrier maintenance (via oxygen consumption in colonocytes). Butyrate literally energizes the gut barrier.
                        Even if butyrate is the primary fuel for colonocytes, allowing them to function optimally and maintain the physical barrier, you won’t have rich-butyrate food (butter) arrive at destination.
                        Food butyrate doesn’t substitute for microbially produced butyrate in the colon. You need help from the microbiota. Dietary butyrate has systemic anti-inflammatory benefits, may support mitochondrial function and is easy on digestion. But dietary butyrate won’t rebuild a damaged gut barrier the way endogenous microbial butyrate does.
                        Also, pamper your commensal bacteria with a varied supply of useful nutrients...
                        Fig 1. Ingested food following the bacterial pathway.png
                        Butyrate is indirectly enhanced by resistant Starch (potato, rice, bread), Inulin (FOS from onions, garlic, asparagus, bananas, leeks), pectin (apple, citrus fruit, carrot), beta-glucan (oat, mushroom), GOS ((legumes, dairy), XOS (fruits, vegetables, whole grains) when the commensal bacteria feeds on these elements. + Yogurt & Kefir…
                        Note that the GABA shunt requires enzymatic reactions: GABA → Succinate = substrate for some bacteria that convert it into butyrate, a key SCFA. It serves as a signaling molecule that modulates immune and epithelial cell activity.
                        As you know probably, SCFAs—especially butyrate and propionate—upregulate junction proteins:
                         Occludin
                         Claudin-1 and -4
                         ZO-1 (zonulin)
                        Result:
                        ✓ Reduced gut permeability
                        ✓ Less endotoxin (LPS) crossing into the bloodstream
                        ✓ Lower systemic inflammation
                        More info on this link:
                        https://mirzoune-ciboulette.forumactif.org/t2153-english-corner-how-is-gaba-powder-useful-for-microbiota#30480

                        1 Reply Last reply Reply Quote 1
                        • A
                          atlee
                          last edited by

                          @LucH said in GABA powder:

                          microbiota

                          Viral episodes since 2020 seem to have had a dramatic (and lingering) negative effect on the oral and digestive microbiome.
                          Although scientific studies seem to be largely contradictory, I would suggest that Lactic Acid producing bacteria have increased and GABA producing bacteria have decreased.
                          For me, this has resulted in apparent abdominal sensitivity to pain and swelling, and episodes of digestive motility blockage. 200-400mg/d GABA powder has a relaxing effect on the nerves and muscles involved in the tension/distension.
                          At the same time, I find that I have to limit Lactic Acid producing foods: fermented ingestibles: no Kimchi, Sauerkraut, Kefir, Buttermilk, Yogurt.
                          And no Lactobacillus Probiotics.

                          LucHL 1 Reply Last reply Reply Quote 1
                          • LucHL
                            LucH @atlee
                            last edited by

                            @atlee said in GABA powder:

                            200-400mg/d GABA powder has a relaxing effect on the nerves and muscles involved in the tension/distension.

                            Yes, indeed but I won't take gaba powder, nor glycine when there is dysbiosis (overgrowth) or unbalance in the microbiota. Why?
                            let's take 2 strains; E. Coli and candida albicans. They can feed on derived molecules. Make a search with the gaba shunt if you want more details.
                            I've explained this pathway in details on my forum.
                            When suffering from overgrowth, the tactics isn't the same.
                            In summary: Weaken – kick and push out.
                            Coordinated and planned tactic, which results in a structured scheme:
                             Weaken (deprivation of resources but not complete abstinence)
                             Organize to knock out (limiting the ability to adapt)
                             Machin-gun (with increased die-off) + assistance to evacuate LPS endotoxins
                             Consolidation (nutrients useful to ensure diversification of commensal bacteria + enhancing peaceful communication through the vagal nerve between the brain and the stomach).
                            Occupy the place (diversified menus and possible contributions of specific strains depending on the terrain, e.g. if you suffer from allergies / histamine intolerance or not.

                            In prevention, get informed on motility (MMC) if your transit is lazy.
                            Need 30 g fiber (progressive) from veggies and fruits, as a substrate.
                            To set things in order, before it's too late: Quercetin, iodine (with a protocol to open NIS symporters and avoid a Wolff-Chaikoff effect).
                            If in crisis, I'd proceed with essential oils. I did it last year with success, when my transit was rather lazy, with flatulencies and sulphur odors. Details are to be found in my log, on my forum (In French; translator needed). Under control. Have still to take care for histamine excess. I manage rather well, though this last point is not ideal.

                            1 Reply Last reply Reply Quote 1
                            • A
                              atlee
                              last edited by

                              Great summary and suggestions. I spent a lot of my RPF years in this neighborhood, and I am very much aligned with your views.
                              I would add to my post that I have had good success with taking half of my 200-400mg/d GABA powder sublingually. It seems to have very significant sublingual uptake, perhaps by avoiding the gut microbiome.

                              1 Reply Last reply Reply Quote 1
                              • P
                                pittybitty
                                last edited by pittybitty

                                So my own experience is that it works and definitely reaches the brain. It will probably help if you are suffering from depression and/or recovering from taking SRIs like Haidut suggested in one interview but it won't have any "general" health effect, it's not some nutrient you would be deficient in. It just makes you very relaxed after a few hours.

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