代谢物
肠道菌群
化学
新陈代谢
脂质代谢
甘油三酯
内分泌学
内科学
糖尿病
胆固醇
药理学
生物化学
生物
医学
作者
Xiaoyue Li,Zhu‐Lin Yu,Ying‐Cai Zhao,Dandan Wang,Changhu Xue,Tiantian Zhang,Yuming Wang
标识
DOI:10.1002/mnfr.202300443
摘要
Scope Gut microbiota can convert a variety of alkaloids and TMAO into TMA, which is then transported by the blood to the liver, and converted into TMAO. In recent years, TMAO has attracted wide attention as a metabolic risk factor in cardiovascular disease, diabetes, and other diseases. However, it is still unclear about the role of gut microbial metabolite TMA in the adverse health impacts of TMAO. Methods and results Male C57BL/6J is treated with intraperitoneal (i.p.) or oral TMAO for 8 weeks, the area under the OGTT curve of oral group is significantly increased by about 15% compared to the control and injection groups. Serum triglyceride levels in the oral group are significantly higher by 28.2% and 24.6% than those in the control and injection groups, respectively. Meanwhile, cholesterol content in serum is significantly elevated by 27.6% and 30.7%. Similarly, proinflammatory factors gene expressions are significantly increased with oral but not i.p. TMAO intervention. Furthermore, transformation in HepG2 cells shows that TMAO could not be converted into TMA by hepatocytes. Conclusion The adverse effects of TMAO on glucose and lipid metabolism in C57BL/6J mice may act through gut microbiota metabolite TMA.
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