Batacan Romeo, Briskey David, Bajagai Yadav Sharma, Smith Chelsie, Stanley Dana, Rao Amanda
School of Health, Medical and Applied Sciences, Central Queensland University, Rockhampton, QLD 4701, Australia.
School of Human Movement and Nutrition Sciences, The University of Queensland, Brisbane, QLD 4006, Australia.
Biomedicines. 2024 Jul 20;12(7):1620. doi: 10.3390/biomedicines12071620.
This study investigates the effects of palmitoylethanolamide (PEA) on the gut microbiome of overweight adults. Fifty-eight participants (twenty males, thirty-eight females) aged 18-65 years with a BMI range of 30-40 kg/m were recruited. Participants were randomised to receive PEA ( = 36) or a placebo ( = 22) for 12 weeks. Microbiota composition, richness, diversity, and metabolic functions, faecal short chain fatty acids and calprotectin, pathology markers, and health-related questionnaires were analysed throughout the 12 weeks of supplementation. PEA supplementation significantly reduced triglyceride levels and IL-2 concentrations. No significant differences were found in the overall microbiota composition between the groups, and microbiota richness and diversity remained consistent for both groups. Functional analysis demonstrated no differences in functional richness and diversity, but specific pathways were modified. PEA supplementation resulted in a decrease in the abundance of pathways related to aromatic compound degradation, NAD interconversion, and L-glutamate degradation, while pathways associated with molybdopterin biosynthesis and O-antigen building blocks exhibited increased abundance. Increased production of O-antigen results in smooth LPS associated with reduced pathogenic stealth and persistence. PEA supplementation may influence specific microbial species, metabolic pathways, and reduce serum triglyceride and IL-2 concentration, shedding light on the intricate relationship between PEA, the microbiome, and host health.
本研究调查了棕榈酰乙醇胺(PEA)对超重成年人肠道微生物群的影响。招募了58名年龄在18 - 65岁之间、BMI范围为30 - 40 kg/m²的参与者(20名男性,38名女性)。参与者被随机分为接受PEA(n = 36)或安慰剂(n = 22)治疗12周。在整个12周的补充期内,分析了微生物群组成、丰富度、多样性和代谢功能、粪便短链脂肪酸和钙卫蛋白、病理标志物以及与健康相关的问卷。补充PEA显著降低了甘油三酯水平和IL - 2浓度。两组之间的总体微生物群组成没有发现显著差异,两组的微生物群丰富度和多样性保持一致。功能分析表明功能丰富度和多样性没有差异,但特定途径发生了改变。补充PEA导致与芳香族化合物降解、NAD相互转化和L - 谷氨酸降解相关的途径丰度降低,而与钼蝶呤生物合成和O抗原构建块相关的途径丰度增加。O抗原产量增加导致与致病性隐匿和持久性降低相关的光滑脂多糖。补充PEA可能会影响特定的微生物种类、代谢途径,并降低血清甘油三酯和IL - 2浓度,揭示了PEA、微生物群和宿主健康之间的复杂关系。