Hormonal
Dihydromyricetin (DHM) supplementation improves insulin resistance and glucose tolerance in high-fat diet-induced mice by modulating gut microbiota to increase chenodeoxycholic acid (CDCA), which inhibits farnesoid X receptor (FXR) expression in intestinal L cells, thereby increasing glucagon gene (Gcg) mRNA expression and enhancing glucagon-like peptide-1 (GLP-1) secretion.
This research suggests that Dihydromyricetin (DHM), a compound found in plants like Ampelopsis grossedentata, may help improve insulin sensitivity and blood sugar control by changing gut bacteria to produce more beneficial bile acids (CDCA). This process boosts GLP-1, a hormone that helps regulate blood sugar. While this was shown in mice fed a high-fat diet, it points to the importance of gut health in metabolic function. For humans, this implies that dietary sources of DHM or gut-health-supporting strategies might be a complementary approach to managing insulin resistance, though human dosing and efficacy are not yet established.
DHM could ameliorate GLP-1 level and insulin resistance by modulation of gut microbiota and the metabolites, particularly the regulation of chenodeoxycholic acid (CDCA) content, followed by the inhibition of farnesoid X receptor (FXR) expression in intestinal L cells and increased glucagon gene (Gcg) mRNA expression and GLP-1 secretion.
Why this rating
The study uses a well-designed animal model with mechanistic depth (transplantation, antibiotic depletion) but lacks human clinical data.
Source
Dihydromyricetin Promotes Glucagon‐Like Peptide‐1 Secretion and Improves Insulin Resistance by Modulation of the Gut Microbiota‐CDCA Pathway
Pengfei Li et al. · Molecular Nutrition & Food Research · 2025
DOI 10.1002/mnfr.202400491
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