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Male castration increases adiposity via small intestinal microbial alterations
Author(s) -
Whon Tae Woong,
Kim Hyun Sik,
Shin NaRi,
Jung Eun Sung,
Tak Euon Jung,
Sung Hojun,
Jung MiJa,
Jeong YunSeok,
Hyun DongWook,
Kim Pil Soo,
Jang Yu Kyung,
Lee Choong Hwan,
Bae JinWoo
Publication year - 2020
Publication title -
embo reports
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 4.584
H-Index - 184
eISSN - 1469-3178
pISSN - 1469-221X
DOI - 10.15252/embr.202050663
Subject(s) - biology , castration , metabolomics , phenotype , gut flora , phenocopy , obesity , medicine , endocrinology , hormone , immunology , genetics , bioinformatics , gene
Castration of young males is widely used in the cattle industry to improve meat quality, but the mechanism linking hypogonadism and host metabolism is not clear. Here, we use metataxonomic and metabolomic approaches to evaluate the intestinal microbiota and host metabolism in male, castrated male (CtM), and female cattle. After pubescence, the CtM cattle harbor distinct ileal microbiota dominated by the family Peptostreptococcaceae and exhibit distinct serum and muscle amino acid profiles (i.e., highly abundant branched‐chain amino acids), with increased extra‐ and intramuscular fat storage. We also evaluate the causative factor(s) that underpin the alteration of the intestinal microbiota and host metabolic phenotype in response to hypogonadism. Castration of male mice phenocopies both the intestinal microbial alterations and obese‐prone metabolism observed in cattle. Antibiotic treatment and fecal microbiota transplantation experiments in a mouse model confirm that the intestinal microbial alterations associated with hypogonadism are a key contributor to the obese phenotype in the CtM animals. Collectively, targeting the gut microbiota is a potential therapeutic strategy for the treatment of both hypogonadism and obesity.

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