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Gut Microbiota Metabolite TMA May Mediate the Effects of TMAO on Glucose and Lipid Metabolism in C57BL/6J Mice. | LitMetric

Gut Microbiota Metabolite TMA May Mediate the Effects of TMAO on Glucose and Lipid Metabolism in C57BL/6J Mice.

Mol Nutr Food Res

SKL of Marine Food Processing & Safety Control, College of Food Science and Engineering, Ocean University of China, No.1299 Sansha Road, Qingdao, Shandong Province, 266404, P. R. China.

Published: March 2024

AI Article Synopsis

  • Gut microbiota convert various alkaloids and TMAO into TMA, which is linked to cardiovascular and metabolic diseases, but the specific role of TMA in health impacts of TMAO remains unclear.
  • In a study with male C57BL/6J mice, oral TMAO treatment for 8 weeks significantly increased glucose and lipid levels, as indicated by higher OGTT curves and elevated triglyceride and cholesterol levels, compared to control groups.
  • The findings suggest that TMAO negatively affects glucose and lipid metabolism in mice potentially through its conversion to TMA by gut microbiota, highlighting the need for further research on this pathway.

Article Abstract

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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Source
http://dx.doi.org/10.1002/mnfr.202300443DOI Listing

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