Alqudah Sara, DeLucia Beckey, Osborn Lucas J, Markley Rachel L, Bobba Viharika, Preston Sarah M, Thambidurai Tharika, Nia Layan Hamidi, Fulmer Clifton G, Sangwan Naseer, Nemet Ina, Claesen Jan
Department of Cardiovascular and Metabolic Sciences, Lerner Research Institute of the Cleveland Clinic; Cleveland, OH, USA.
Center for Microbiome and Human Health, Lerner Research Institute of the Cleveland Clinic; Cleveland, OH, USA.
bioRxiv. 2025 May 18:2025.05.18.654739. doi: 10.1101/2025.05.18.654739.
Obesity-associated metabolic disorders such as type 2 diabetes mellitus and metabolic dysfunction associated fatty liver disease are major global health concerns, yet current pharmacological treatments often present with major side-effects. Dietary interventions including polyphenol-rich foods offer a promising complementary option for obesity amelioration, but their efficacy is dependent on specific gut microbial metabolism and the underlying molecular mechanisms mostly remain elusive. Here, we demonstrated that dietary elderberry (Eld) extract abrogates the effects of an obesogenic diet in a gut microbiota-dependent manner, by preventing insulin resistance and reducing hepatic steatosis in mice. We developed a targeted, quantitative liquid chromatography-tandem mass spectrometry method for detection of gut bacterial polyphenol catabolites and identified hydrocinnamic acid as a key microbial metabolite, enriched in the portal vein plasma of Eld supplemented animals. Next, we showed that hydrocinnamic acid potently activates hepatic AMP-activated protein kinase α, explaining its role in improved liver lipid homeostasis. Furthermore, we uncovered the metabolic pathway cumulating in hydrocinnamic acid production in the common gut commensal . Our characterization of hydrocinnamic acid as a diet-derived, and microbiota-dependent metabolite with insulin-sensitizing and anti-steatotic activities will contribute to microbiome-targeted dietary interventions to prevent and treat obesity-associated metabolic diseases.
肥胖相关的代谢紊乱,如2型糖尿病和代谢功能障碍相关脂肪性肝病,是全球主要的健康问题,但目前的药物治疗往往存在严重的副作用。包括富含多酚的食物在内的饮食干预为改善肥胖提供了一种有前景的补充选择,但其功效取决于特定的肠道微生物代谢,其潜在的分子机制大多仍不清楚。在这里,我们证明了膳食接骨木提取物通过预防小鼠胰岛素抵抗和减少肝脏脂肪变性,以肠道微生物群依赖的方式消除致肥胖饮食的影响。我们开发了一种靶向定量液相色谱-串联质谱法来检测肠道细菌多酚分解代谢物,并确定氢化肉桂酸是一种关键的微生物代谢物,在补充接骨木提取物的动物的门静脉血浆中含量丰富。接下来,我们表明氢化肉桂酸能有效激活肝脏中的AMP激活蛋白激酶α,解释了其在改善肝脏脂质稳态中的作用。此外,我们还揭示了普通肠道共生菌中积累氢化肉桂酸的代谢途径。我们将氢化肉桂酸表征为一种具有胰岛素增敏和抗脂肪变性活性的饮食来源且依赖微生物群的代谢物,这将有助于以微生物群为靶点的饮食干预,以预防和治疗肥胖相关的代谢疾病。