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Relationship between gut environment, feces-to-food ratio, and androgen deficiency-induced metabolic disorders

Androgen action generates sex-related differences that include changes in the gut microbiota composition. Hypoandrogenism and hyperandrogenism in males and females, respectively, are associated with the prevalence of metabolic disorders. Our recent work showed that male androgen receptor knockout (A...

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Autores principales: Harada, Naoki, Minami, Yukari, Hanada, Kazuki, Hanaoka, Ryo, Kobayashi, Yasuyuki, Izawa, Takeshi, Sato, Takashi, Kato, Shigeaki, Inui, Hiroshi, Yamaji, Ryoichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7781658/
https://www.ncbi.nlm.nih.gov/pubmed/32991827
http://dx.doi.org/10.1080/19490976.2020.1817719
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author Harada, Naoki
Minami, Yukari
Hanada, Kazuki
Hanaoka, Ryo
Kobayashi, Yasuyuki
Izawa, Takeshi
Sato, Takashi
Kato, Shigeaki
Inui, Hiroshi
Yamaji, Ryoichi
author_facet Harada, Naoki
Minami, Yukari
Hanada, Kazuki
Hanaoka, Ryo
Kobayashi, Yasuyuki
Izawa, Takeshi
Sato, Takashi
Kato, Shigeaki
Inui, Hiroshi
Yamaji, Ryoichi
author_sort Harada, Naoki
collection PubMed
description Androgen action generates sex-related differences that include changes in the gut microbiota composition. Hypoandrogenism and hyperandrogenism in males and females, respectively, are associated with the prevalence of metabolic disorders. Our recent work showed that male androgen receptor knockout (ARKO) mice developed high-fat diet (HFD)-dependent sarcopenic abdominal obesity, hyperglycemia, and hepatic steatosis, leading to early death. The ARKO mice also exhibited alterations in intestinal microbiota but did not experience metabolic abnormalities when administered with antibiotics. Here, we show that time-dependent changes in feed efficiency (ratio of body weight gain to food intake) and weight of dried feces-to-food ratio could be good markers for changes in gut microbiota. Turicibacter spp., Lactobacillus spp., and L. reuteri increased in the gut in both HFD-fed ARKO and castrated mice having metabolic abnormalities. HFD-fed ARKO mice showed increased plasma levels of aspartate, but not alanine, aminotransferase. Changes in the gut microbiome appear to provoke androgen deficiency-induced metabolic diseases, leading to early mortality.
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spelling pubmed-77816582021-01-14 Relationship between gut environment, feces-to-food ratio, and androgen deficiency-induced metabolic disorders Harada, Naoki Minami, Yukari Hanada, Kazuki Hanaoka, Ryo Kobayashi, Yasuyuki Izawa, Takeshi Sato, Takashi Kato, Shigeaki Inui, Hiroshi Yamaji, Ryoichi Gut Microbes Addendum Androgen action generates sex-related differences that include changes in the gut microbiota composition. Hypoandrogenism and hyperandrogenism in males and females, respectively, are associated with the prevalence of metabolic disorders. Our recent work showed that male androgen receptor knockout (ARKO) mice developed high-fat diet (HFD)-dependent sarcopenic abdominal obesity, hyperglycemia, and hepatic steatosis, leading to early death. The ARKO mice also exhibited alterations in intestinal microbiota but did not experience metabolic abnormalities when administered with antibiotics. Here, we show that time-dependent changes in feed efficiency (ratio of body weight gain to food intake) and weight of dried feces-to-food ratio could be good markers for changes in gut microbiota. Turicibacter spp., Lactobacillus spp., and L. reuteri increased in the gut in both HFD-fed ARKO and castrated mice having metabolic abnormalities. HFD-fed ARKO mice showed increased plasma levels of aspartate, but not alanine, aminotransferase. Changes in the gut microbiome appear to provoke androgen deficiency-induced metabolic diseases, leading to early mortality. Taylor & Francis 2020-09-29 /pmc/articles/PMC7781658/ /pubmed/32991827 http://dx.doi.org/10.1080/19490976.2020.1817719 Text en © 2020 The Author(s). Published with license by Taylor & Francis Group, LLC. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Addendum
Harada, Naoki
Minami, Yukari
Hanada, Kazuki
Hanaoka, Ryo
Kobayashi, Yasuyuki
Izawa, Takeshi
Sato, Takashi
Kato, Shigeaki
Inui, Hiroshi
Yamaji, Ryoichi
Relationship between gut environment, feces-to-food ratio, and androgen deficiency-induced metabolic disorders
title Relationship between gut environment, feces-to-food ratio, and androgen deficiency-induced metabolic disorders
title_full Relationship between gut environment, feces-to-food ratio, and androgen deficiency-induced metabolic disorders
title_fullStr Relationship between gut environment, feces-to-food ratio, and androgen deficiency-induced metabolic disorders
title_full_unstemmed Relationship between gut environment, feces-to-food ratio, and androgen deficiency-induced metabolic disorders
title_short Relationship between gut environment, feces-to-food ratio, and androgen deficiency-induced metabolic disorders
title_sort relationship between gut environment, feces-to-food ratio, and androgen deficiency-induced metabolic disorders
topic Addendum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7781658/
https://www.ncbi.nlm.nih.gov/pubmed/32991827
http://dx.doi.org/10.1080/19490976.2020.1817719
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