The gut microbiota changed by ketogenic diets contribute to glucose intolerance rather than lipid accumulation

Front Endocrinol (Lausanne). 2024 Sep 27:15:1446287. doi: 10.3389/fendo.2024.1446287. eCollection 2024.

Abstract

The ketogenic diet (KD) is a popular option for managing body weight, though its influence on glucose and lipid metabolism was still inconclusive. Gut microbiota is modulated by dietary pattens and has been associated with the changes of metabolic homeostasis induced by KD. Here, we found that two types of KDs, KD1 (8.8% carbohydrate, 73.4% fat, 17.9% protein, 5.7 kcal/g) and KD2 (0.4% carbohydrate, 93.2% fat, 6.4% protein, 6.7 kcal/g), induced changes of gut microbiota and its metabolites, contributing to glucose intolerance but not lipid accumulation in mice. Following a 2-week intervention with KDs, mice fed on KD1 displayed symptoms related to obesity, whereas KD2-fed mice exhibited a decrease in body weight but had severe hepatic lipid accumulation and abnormal fatty acid metabolism, while both KDs led to significant glucose intolerance. Compared to the mice fed on a standard chow diet, the conventional mice fed on both KD1 and KD2 had significant shifted gut microbiota, lower levels of short chain fatty acids (SCFAs) and composition alteration of cecal bile acids. By using an antibiotic cocktail (ABX) to deplete most of the gut microbiota in mice, we found the disturbances induced by KDs in lipid metabolism were similar in the ABX-treated mice to their conventional companions, but the disturbances in glucose metabolism were absent in the ABX-treated mice. In conclusion, these findings suggest that ketogenic diets disrupted glucose and lipid metabolism, at least in mice, and highlight the gut microbial culprits associated with KD induced glucose intolerance rather than lipid accumulation.

Keywords: SCFA; bile acid; glucose and lipid metabolism; gut microbiota; ketogenic diet.

MeSH terms

  • Animals
  • Diet, Ketogenic* / adverse effects
  • Gastrointestinal Microbiome* / drug effects
  • Glucose Intolerance* / etiology
  • Glucose Intolerance* / metabolism
  • Lipid Metabolism* / drug effects
  • Liver / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL*
  • Obesity / etiology
  • Obesity / metabolism
  • Obesity / microbiology

Grants and funding

The author(s) declare financial support was received for the research, authorship, and/or publication of this article. This work was supported by grants from the National Key Research and Development Project (2022YFF1100103 and 2019YFA0905602) and the National Natural Science Foundation of China (31922003 and 81871091).