生酮饮食诱导胆汁酸通过减少热量吸收防止肥胖

IF 18.9 1区 医学 Q1 ENDOCRINOLOGY & METABOLISM Nature metabolism Pub Date : 2024-06-27 DOI:10.1038/s42255-024-01072-1
Xiao Li, Jie Yang, Xiaofeng Zhou, Chen Dai, Mengmeng Kong, Linshan Xie, Chenglin Liu, Yilian Liu, Dandan Li, Xiaonan Ma, Yuxiang Dai, Yan Sun, Zhijie Jian, Xiaohuan Guo, Xu Lin, Yixue Li, Liang Sun, Xin Liu, Li Jin, Huiru Tang, Yan Zheng, Shangyu Hong
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摘要

长期以来,人们一直采用低碳水化合物生酮饮食(KD)来减肥,但其基本机制仍难以捉摸。有人认为肠道微生物群和代谢物介导了摄入 KD 引起的代谢变化,但具体涉及哪些肠道微生物或代谢物尚不清楚。在这里,我们发现食用 KD 会提高小鼠血清中牛磺酸去氧胆酸(TDCA)和牛磺酸去氧胆酸(TUDCA)的水平,从而降低体重和空腹血糖水平。从机理上讲,喂食 KD 会降低编码胆盐水解酶 (BSH) 的肠道细菌鼠乳杆菌 ASF361 的丰度。L. murinus ASF361 的减少或 BSH 活性的抑制会增加 TDCA 和 TUDCA 的循环水平,从而通过抑制肠道碳酸酐酶 1 的表达来减少能量吸收,导致体重减轻。研究发现,在多种小鼠模型中,TDCA 和 TUDCA 治疗可防止肥胖及其并发症。此外,在一项针对健康人类参与者(n = 416)的观察性研究中,以及一项针对超重或肥胖参与者(n = 25)的低碳水化合物 KD 干预性研究中,都持续观察到了上述胆汁酸、微生物 BSH 和代谢特征之间的关联。总之,我们发现了一种独特的宿主-肠道微生物群代谢相互作用机制,即食用 KD 可降低体重和空腹血糖水平。我们的研究结果支持将 TDCA 和 TUDCA 作为 KD 之外的两种治疗肥胖症及其并发症的候选药物。
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Ketogenic diet-induced bile acids protect against obesity through reduced calorie absorption
The low-carbohydrate ketogenic diet (KD) has long been practiced for weight loss, but the underlying mechanisms remain elusive. Gut microbiota and metabolites have been suggested to mediate the metabolic changes caused by KD consumption, although the particular gut microbes or metabolites involved are unclear. Here, we show that KD consumption enhances serum levels of taurodeoxycholic acid (TDCA) and tauroursodeoxycholic acid (TUDCA) in mice to decrease body weight and fasting glucose levels. Mechanistically, KD feeding decreases the abundance of a bile salt hydrolase (BSH)-coding gut bacterium, Lactobacillus murinus ASF361. The reduction of L. murinus ASF361 or inhibition of BSH activity increases the circulating levels of TDCA and TUDCA, thereby reducing energy absorption by inhibiting intestinal carbonic anhydrase 1 expression, which leads to weight loss. TDCA and TUDCA treatments have been found to protect against obesity and its complications in multiple mouse models. Additionally, the associations among the abovementioned bile acids, microbial BSH and metabolic traits were consistently observed both in an observational study of healthy human participants (n = 416) and in a low-carbohydrate KD interventional study of participants who were either overweight or with obesity (n = 25). In summary, we uncover a unique host–gut microbiota metabolic interaction mechanism for KD consumption to decrease body weight and fasting glucose levels. Our findings support TDCA and TUDCA as two promising drug candidates for obesity and its complications in addition to a KD. A ketogenic diet can reduce calorie absorption and protect against obesity by inducing changes to the gut microbiota and the bile acid pool.
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来源期刊
Nature metabolism
Nature metabolism ENDOCRINOLOGY & METABOLISM-
CiteScore
27.50
自引率
2.40%
发文量
170
期刊介绍: Nature Metabolism is a peer-reviewed scientific journal that covers a broad range of topics in metabolism research. It aims to advance the understanding of metabolic and homeostatic processes at a cellular and physiological level. The journal publishes research from various fields, including fundamental cell biology, basic biomedical and translational research, and integrative physiology. It focuses on how cellular metabolism affects cellular function, the physiology and homeostasis of organs and tissues, and the regulation of organismal energy homeostasis. It also investigates the molecular pathophysiology of metabolic diseases such as diabetes and obesity, as well as their treatment. Nature Metabolism follows the standards of other Nature-branded journals, with a dedicated team of professional editors, rigorous peer-review process, high standards of copy-editing and production, swift publication, and editorial independence. The journal has a high impact factor, has a certain influence in the international area, and is deeply concerned and cited by the majority of scholars.
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