4.5 Article

Excess Growth Hormone Alters the Male Mouse Gut Microbiome in an Age-dependent Manner

期刊

ENDOCRINOLOGY
卷 163, 期 7, 页码 -

出版社

ENDOCRINE SOC
DOI: 10.1210/endocr/bqac074

关键词

growth hormone; bGH mice; longitudinal gut microbiome; short-chain fatty acids

资金

  1. National Institutes of Health (NIH) [AG059779]
  2. John J. Kopchick Molecular and Cellular Biology/Translational Biomedical Sciences Research Fellowship
  3. Osteopathic Heritage Foundations
  4. Dual Degree Program at Ohio University Heritage College of Osteopathic Medicine
  5. NIH [U24-DK092993]
  6. Host Response core of Mouse Metabolic Phenotyping Center at UC

向作者/读者索取更多资源

The gut microbiome is influenced by growth hormone, with excess GH leading to changes in microbial composition and impaired fat absorption in mice. This study provides insights into the age-dependent effects of excess GH on the gut microbiome and its metabolic pathways.
The gut microbiome has an important role in host development, metabolism, growth, and aging. Recent research points toward potential crosstalk between the gut microbiota and the growth hormone (GH)/insulin-like growth factor-1 (IGF-1) axis. Our laboratory previously showed that GH excess and deficiency are associated with an altered gut microbial composition in adult mice. Yet, no study to date has examined the influence of GH on the gut microbiome over time. Our study thus tracked the effect of excess GH action on the longitudinal changes in the gut microbial profile (ie, abundance, diversity/maturity, predictive metabolic function, and short-chain fatty acid [SCFA] levels) of bovine GH (bGH) transgenic mice at age 3, 6, and 12 months compared to littermate controls in the context of metabolism, intestinal phenotype, and premature aging. The bGH mice displayed age-dependent changes in microbial abundance, richness, and evenness. Microbial maturity was significantly explained by genotype and age. Moreover, several bacteria (ie, Lactobacillus, Lachnospiraceae, Bifidobacterium, and Faecalibaculum), predictive metabolic pathways (such as SCFA, vitamin B-12, folate, menaquinol, peptidoglycan, and heme B biosynthesis), and SCFA levels (acetate, butyrate, lactate, and propionate) were consistently altered across all 3 time points, differentiating the longitudinal bGH microbiome from controls. Of note, the bGH mice also had significantly impaired intestinal fat absorption with increased fecal output. Collectively, these findings suggest that excess GH alters the gut microbiome in an age-dependent manner with distinct longitudinal microbial and predicted metabolic pathway signatures.

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