--- source_url: https://hangovr180.com/science/dhm/brain-aging.md canonical_url: https://hangovr180.com/science/dhm/brain-aging generated_at: 2026-06-28T19:53:17Z build_id: ebfcfef page_type: science-leaf claim_ids: [SF-26, SF-23, SF-18] --- # DHM AND BRAIN AGING *Brain aging is a separate conversation from alcohol metabolism, and the DHM neuroprotection literature is small but consistent across labs and crosses into Alzheimer's models.* These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. ## A Different Conversation Than Alcohol Most of what we publish about DHM is about alcohol -- how it gets metabolized, how it touches the GABA-A receptor, how it changes what you feel the next day. The brain aging research is a separate line of investigation. It started in animal models of Alzheimer's disease and expanded into broader neurodegeneration and oxidative-stress aging models, and the findings are surprisingly consistent across labs[1]. DHM crosses the blood-brain barrier. That is the first thing to know, because most flavonoids don't, or do so poorly. A 2021 mass-spec study identified intact DHM and its primary metabolites in the brain tissue of mice after oral dosing, with kinetics that lined up with the behavioral effects researchers had been measuring[2]. ## Two Mechanisms in the Aging Brain The first mechanism is anti-inflammatory. Microglia, the immune cells of the brain, get progressively more activated with age, and chronic microglial activation is one of the cellular signatures of aging brain tissue. (this is something I had to read three times before it really clicked, honestly.) In APP/PS1 transgenic mice -- a standard Alzheimer's model -- DHM suppressed activation of the NLRP3 inflammasome in microglia and reduced markers of neuroinflammation[3]. > **Claim [SF-26]:** Protects against occasional neuroinflammation. † > > † These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. The second mechanism is energetic. DHM activates the AMPK/SIRT1 signaling pathway, which in plain terms means it pushes brain cells toward the metabolic state they sit in when young and well-rested, rather than the state they drift into with age and stress. The same study that mapped this in Alzheimer's-model rats also showed reduced hippocampal cell death and improved cognitive performance on standard maze tasks[4]. ## What "Attenuates Brain Aging" Actually Means > **Claim [SF-23]:** Attenuates the rate of brain aging. † > > † These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. Brain aging in animal studies is typically operationalized as a combination of cognitive performance, oxidative stress markers, neuroinflammation markers, and synaptic protein levels. DHM moves all four of those measures in the right direction in the published mouse data, in the studies that have looked, at least. > **Claim [SF-18]:** Promotes brain health and cognitive function. † > > † These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. That is not the same as "DHM prevents Alzheimer's in humans." We do not have human clinical trials at that scale, and we should not pretend we do. What we have is a body of preclinical work showing the mechanisms are real, the compound reaches the relevant tissue, and the behavioral outcomes in animals improve in directions that are consistent with brain-protective effects. ## Why I Care About This Personally I am 50-plus, and my interest in this category started with hangovers but extended pretty quickly into what alcohol does to the brain over decades. One of the more uncomfortable things you learn going through the alcohol-and-brain literature is how much of the cognitive cost of drinking is cumulative rather than acute. DHM is one of the few compounds in the supplement world where the brain-aging research and the alcohol research overlap in mechanism, which is part of why we built the formula around it. The 2020 Liang study on DHM and the hippocampus also looked at gephyrin, a scaffolding protein that holds GABA-A receptors at the synapse, and found that DHM helps preserve gephyrin levels under chronic alcohol stress[5]. Synaptic infrastructure matters more for long-term cognitive function than most people realize, and seeing a single compound that moves both inflammation markers adn synaptic structure in the same direction is unusual. ## What This Page Is Not Claiming DHM is not a cognitive enhancer. The brain-aging research is preclinical, not clinical, and the supplement industry routinely overstates what animal data implies about human outcomes. We include DHM in the formula primarily for its alcohol-related effects, with the brain-aging research as a supporting line of evidence rather than the headline claim. For the alcohol-metabolism side, see [How DHM Works: The ADH/ALDH Pathway](/science/dhm/adh-aldh-pathway). For the GABA mechanism, see [DHM and GABA Modulation](/science/dhm/gaba-modulation). ## Citations 1. Carry E, et al. [Preclinical Research of Dihydromyricetin for Brain Aging and Neurodegenerative Diseases](https://pmc.ncbi.nlm.nih.gov/articles/PMC6859532/). PMC6859532. 2. Silva J, et al. [Identification of Dihydromyricetin and Metabolites in Serum and Brain Associated with Acute Anti-Ethanol Intoxicating Effects in Mice](https://pmc.ncbi.nlm.nih.gov/articles/PMC8307506/). PMC8307506. 3. Feng J, et al. [Dihydromyricetin Inhibits Microglial Activation and Neuroinflammation by Suppressing NLRP3 Inflammasome Activation in APP/PS1 Transgenic Mice](https://pmc.ncbi.nlm.nih.gov/articles/PMC6282966/). PMC6282966. 4. Sun P, et al. [Protective Role of Dihydromyricetin in Alzheimer's Disease Rat Model Associated with Activating AMPK/SIRT1 Signaling Pathway](https://pmc.ncbi.nlm.nih.gov/articles/PMC6328867/). PMC6328867. 5. Liang J, et al. [Modulation of Hippocampal GABAergic Neurotransmission and Gephyrin Levels by Dihydromyricetin Improves Anxiety](https://pmc.ncbi.nlm.nih.gov/articles/PMC7364153/). PMC7364153. ## Read Next - [How DHM Works -- The ADH/ALDH Pathway](/science/dhm/adh-aldh-pathway) - [DHM and GABA Modulation](/science/dhm/gaba-modulation) - [DHM Dose-Response -- Why 1,500mg](/science/dhm/dose-response) - [DHM -- The Hub](/science/dhm) **Written by Mark Scott** - Co-Formulator, Hangovr180® | Co-Inventor, [US Application 18/698,010](https://patents.google.com/patent/US20250073201A1) Mark Scott conducted approximately 150 personal formulation tests over six months to develop the H180 ingredient combination. [Editorial standards](/editorial-standards) --- These statements have not been evaluated by the Food and Drug Administration. This product is not intended to diagnose, treat, cure, or prevent any disease. Hangovr180® is a dietary supplement. Individual results may vary. Consult your healthcare provider before use if you have any medical conditions or take medications. [US Application 18/698,010](https://patents.google.com/patent/US20250073201A1). Canonical: https://hangovr180.com/science/dhm/brain-aging