Shen Jinxin, Zhou Yi, Yang Daijun, Liu Ruonan, Zhu Xiaoling, Liu Rui
College of Food Science and Technology, Huazhong Agricultural University, Wuhan 430070, China.
Hubei Provincial Institute for Food Supervision and Test, Wuhan 430075, China.
Nutrients. 2025 Jul 5;17(13):2228. doi: 10.3390/nu17132228.
: Obesity-associated metabolic disorders represent a critical global health challenge, which necessitates innovative strategies targeting lipid metabolism. Peanut skin procyanidins (PSPs), abundant bioactive compounds derived from agricultural by-products, show potential in lipid regulation, but molecular mechanisms remain unclear. : This study integrated hepatic metabolomics, network pharmacology, and gut microbiota analysis to systematically decipher the mechanisms for PSP to ameliorate high-fat diet (HFD)-induced lipid metabolism disorders. : PSP intervention significantly attenuated HFD-induced increases in LDL-C, TG, and TC levels and effectively mitigated hepatic lipid accumulation. Metabolomics revealed that PSP reshaped hepatic lipid dynamics by modulating glycerophospholipid, linoleic acid, arachidonic acid, tryptophan, and nitrogen metabolism. Subsequent network pharmacology identified , , , and as the core targets, and PSP could markedly suppress their HFD-induced overexpression. Furthermore, PSP selectively reshaped the gut microbiota, enriching beneficial genera such as and while reducing the abundance of harmful bacteria within Firmicutes. PICRUSt-based functional prediction indicated that PSP alters gut microbial glutamine synthetase activity. : Mechanistically, PSP regulates lipid metabolism by downregulating , , , and expression, remodeling gut microbiota structure, and increasing hepatic glutamine level. These findings provide novel insights into value-added utilization of agricultural byproducts and development of targeted intervention strategies for metabolic diseases.
肥胖相关的代谢紊乱是一项严峻的全球健康挑战,这需要针对脂质代谢的创新策略。花生皮原花青素(PSP)是源自农业副产品的丰富生物活性化合物,在脂质调节方面显示出潜力,但分子机制仍不清楚。本研究整合了肝脏代谢组学、网络药理学和肠道微生物群分析,以系统地解读PSP改善高脂饮食(HFD)诱导的脂质代谢紊乱的机制。PSP干预显著减轻了HFD诱导的低密度脂蛋白胆固醇(LDL-C)、甘油三酯(TG)和总胆固醇(TC)水平升高,并有效减轻了肝脏脂质积累。代谢组学表明,PSP通过调节甘油磷脂、亚油酸、花生四烯酸、色氨酸和氮代谢来重塑肝脏脂质动态。随后的网络药理学确定[具体基因名称1]、[具体基因名称2]、[具体基因名称3]和[具体基因名称4]为核心靶点,并且PSP可以显著抑制它们在HFD诱导下的过表达。此外,PSP选择性地重塑肠道微生物群,富集有益菌属如[有益菌属名称1]和[有益菌属名称2],同时降低厚壁菌门内有害细菌的丰度。基于PICRUSt的功能预测表明,PSP改变肠道微生物谷氨酰胺合成酶活性。从机制上讲,PSP通过下调[具体基因名称1]、[具体基因名称2]、[具体基因名称3]和[具体基因名称4]的表达、重塑肠道微生物群结构以及提高肝脏谷氨酰胺水平来调节脂质代谢。这些发现为农业副产品的增值利用和代谢疾病靶向干预策略的开发提供了新的见解。