4.7 Article

Roux-en-Y gastric bypass surgery in Zucker rats induces bacterial and systemic metabolic changes independent of caloric restriction-induced weight loss

期刊

GUT MICROBES
卷 13, 期 1, 页码 -

出版社

TAYLOR & FRANCIS INC
DOI: 10.1080/19490976.2021.1875108

关键词

Bariatric surgery; bile acids; metabolism; microbiota; microbiome

资金

  1. Diabetes Research & Wellness Foundation
  2. Interdisciplinary Centre for Clinical Research (IZKF) [Z-3/44]
  3. Medical Research Council New Investigator Grant [MR/L009803/1]
  4. European Research Council (ERC) Starting Grant [715662]
  5. STRATiGRAD doctoral training program at Imperial College London
  6. Pre-clinical Staff Scholarship at Faculty of Medicine, Khon Kaen University
  7. Department of Jobs, Tourism, Science and Innovation, Government of Western Australian Premier's Fellowship
  8. NIHR Imperial Biomedical Research Centre (BRC)
  9. MRC [MR/P002536/1] Funding Source: UKRI

向作者/读者索取更多资源

The study investigated weight loss-independent bacterial and metabolic changes following RYGB surgery, discovering distinct metabolic and bacterial disturbances induced by the surgery. These findings provide insights into potential therapeutic targets for metabolic diseases.
Mechanisms of Roux-en-Y gastric bypass (RYGB) surgery are not fully understood. This study aimed to investigate weight loss-independent bacterial and metabolic changes, as well as the absorption of bacterial metabolites and bile acids through the hepatic portal system following RYGB surgery. Three groups of obese Zucker (fa/fa) rats were included: RYGB (n = 11), sham surgery and body weight matched with RYGB (Sham-BWM, n = 5), and sham surgery fed ad libitum (Sham-obese, n = 5). Urine and feces were collected at multiple time points, with portal vein and peripheral blood obtained at the end of the study. Metabolic phenotyping approaches and 16S rRNA gene sequencing were used to determine the biochemical and bacterial composition of the samples, respectively. RYGB surgery-induced distinct metabolic and bacterial disturbances, which were independent of weight loss through caloric restriction. RYGB resulted in lower absorption of phenylalanine and choline, and higher urinary concentrations of host-bacterial co-metabolites (e.g., phenylacetylglycine, indoxyl sulfate), together with higher fecal trimethylamine, suggesting enhanced bacterial aromatic amino acid and choline metabolism. Short chain fatty acids (SCFAs) were lower in feces and portal vein blood from RYGB group compared to Sham-BWM, accompanied with lower abundances of Lactobacillaceae, and Ruminococcaceae known to contain SCFA producers, indicating reduced bacterial fiber fermentation. Fecal gamma -amino butyric acid (GABA) was found in higher concentrations in RYGB than that in Sham groups and could play a role in the metabolic benefits associated with RYGB surgery. While no significant difference in urinary BA excretion, RYGB lowered both portal vein and circulating BA compared to Sham groups. These findings provide a valuable resource for how dynamic, multi-systems changes impact on overall metabolic health, and may provide potential therapeutic targets for developing downstream non-surgical treatment for metabolic disease.

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