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高脂饮食可能通过诱导微生物群失调增加胰岛素抵抗的风险。

High-fat diet may increase the risk of insulin resistance by inducing dysbiosis.

作者信息

Abbasi Ebrahim, Khodadadi Iraj

机构信息

Nutrition Health Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.

出版信息

Metabol Open. 2025 Jul 22;27:100381. doi: 10.1016/j.metop.2025.100381. eCollection 2025 Sep.

Abstract

High-fat diet (HFD) poses various health risks, such as obesity, insulin resistance (IR), fatty liver, gut microbiota dysbiosis, cognitive impairment, inflammation, and oxidative stress. HFD can alter gastrointestinal function and structure, resulting in changes of the intestinal mucosa, gastric secretions, intestinal connective tissue, intestinal motility, intestinal metabolomics profiles, and intestinal microbiota. The intestine and its microbiota process nutrients and produce molecules that can regulate insulin action and secretion. Changes in the gut microbiome (dysbiosis) and their products may have long-term effects that are not fully understood. Gut microbiota have long been documented to induce metabolic endotoxemia by releasing lipopolysaccharide, which causes systemic inflammation and insulin resistance (IR). HFD may has direct roles in the development of insulin resistance (IR). HFD can induce dysbiosis by reducing SCFAs and decreasing the activation of free fatty acid receptors (FFARs). Furthermore, HFD can increase the activation of the toll-like receptor (TLR) pathway. Hence, HFD by inducing inflammation, oxidative stress, endotoxemia, and hyperglycemia can increase the risk of IR. Therefore, this review aims to delineate the role of gut microbiota directly or indirectly involved in HFD-induced IR. These findings may clarify valuable preventive and therapeutic targets for countermeasures to IR in people who use the Western diet.

摘要

高脂饮食(HFD)会带来各种健康风险,如肥胖、胰岛素抵抗(IR)、脂肪肝、肠道微生物群失调、认知障碍、炎症和氧化应激。高脂饮食会改变胃肠道功能和结构,导致肠黏膜、胃分泌物、肠道结缔组织、肠道蠕动、肠道代谢组学谱和肠道微生物群发生变化。肠道及其微生物群处理营养物质并产生可调节胰岛素作用和分泌的分子。肠道微生物群的变化(失调)及其产物可能具有尚未完全了解的长期影响。长期以来,有文献记载肠道微生物群通过释放脂多糖诱导代谢性内毒素血症,从而导致全身炎症和胰岛素抵抗(IR)。高脂饮食可能在胰岛素抵抗(IR)的发展中起直接作用。高脂饮食可通过减少短链脂肪酸和降低游离脂肪酸受体(FFARs)的激活来诱导失调。此外,高脂饮食可增加Toll样受体(TLR)途径的激活。因此,高脂饮食通过诱导炎症、氧化应激、内毒素血症和高血糖症会增加胰岛素抵抗的风险。因此,本综述旨在阐明肠道微生物群直接或间接参与高脂饮食诱导的胰岛素抵抗的作用。这些发现可能会为采用西方饮食的人群对抗胰岛素抵抗的预防和治疗措施阐明有价值的靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40e4/12309925/2d23cf19d11b/gr1.jpg

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