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Unsuppressed lipolysis in adipocytes is linked with enhanced gluconeogenesis and altered bile acid physiology in Insr(P1195L/+) mice fed high-fat-diet

High-fat diet (HFD) triggers insulin resistance and diabetes mellitus, but their link remains unclear. Characterization of overt hyperglycemia in insulin receptor mutant (Insr(P1195L/+)) mice exposed to HFD (Insr(P1195L/+)/HFD mice) revealed increased glucose-6-phosphatase (G6pc) expression in liver...

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Autores principales: Lee, Eun Young, Sakurai, Kenichi, Zhang, Xilin, Toda, Chitoku, Tanaka, Tomoaki, Jiang, Meizi, Shirasawa, Takuji, Tachibana, Kaori, Yokote, Koutaro, Vidal-Puig, Antonio, Minokoshi, Yasuhiko, Miki, Takashi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4663474/
https://www.ncbi.nlm.nih.gov/pubmed/26615883
http://dx.doi.org/10.1038/srep17565
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author Lee, Eun Young
Sakurai, Kenichi
Zhang, Xilin
Toda, Chitoku
Tanaka, Tomoaki
Jiang, Meizi
Shirasawa, Takuji
Tachibana, Kaori
Yokote, Koutaro
Vidal-Puig, Antonio
Minokoshi, Yasuhiko
Miki, Takashi
author_facet Lee, Eun Young
Sakurai, Kenichi
Zhang, Xilin
Toda, Chitoku
Tanaka, Tomoaki
Jiang, Meizi
Shirasawa, Takuji
Tachibana, Kaori
Yokote, Koutaro
Vidal-Puig, Antonio
Minokoshi, Yasuhiko
Miki, Takashi
author_sort Lee, Eun Young
collection PubMed
description High-fat diet (HFD) triggers insulin resistance and diabetes mellitus, but their link remains unclear. Characterization of overt hyperglycemia in insulin receptor mutant (Insr(P1195L/+)) mice exposed to HFD (Insr(P1195L/+)/HFD mice) revealed increased glucose-6-phosphatase (G6pc) expression in liver and increased gluconeogenesis from glycerol. Lipolysis in white adipose tissues (WAT) and lipolysis-induced blood glucose rise were increased in Insr(P1195L/+)/HFD mice, while wild-type WAT transplantation ameliorated the hyperglycemia and the increased G6pc expression. We found that the expressions of genes involved in bile acid (BA) metabolism were altered in Insr(P1195L/+)/HFD liver. Among these, the expression of Cyp7a1, a BA synthesis enzyme, was insulin-dependent and was markedly decreased in Insr(P1195L/+)/HFD liver. Reduced Cyp7a1 expression in Insr(P1195L/+)/HFD liver was rescued by WAT transplantation, and the expression of Cyp7a1 was suppressed by glycerol administration in wild-type liver. These findings suggest that unsuppressed lipolysis in adipocytes elicited by HFD feeding is linked with enhanced gluconeogenesis from glycerol and with alterations in BA physiology in Insr(P1195L/+)/HFD liver.
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spelling pubmed-46634742015-12-03 Unsuppressed lipolysis in adipocytes is linked with enhanced gluconeogenesis and altered bile acid physiology in Insr(P1195L/+) mice fed high-fat-diet Lee, Eun Young Sakurai, Kenichi Zhang, Xilin Toda, Chitoku Tanaka, Tomoaki Jiang, Meizi Shirasawa, Takuji Tachibana, Kaori Yokote, Koutaro Vidal-Puig, Antonio Minokoshi, Yasuhiko Miki, Takashi Sci Rep Article High-fat diet (HFD) triggers insulin resistance and diabetes mellitus, but their link remains unclear. Characterization of overt hyperglycemia in insulin receptor mutant (Insr(P1195L/+)) mice exposed to HFD (Insr(P1195L/+)/HFD mice) revealed increased glucose-6-phosphatase (G6pc) expression in liver and increased gluconeogenesis from glycerol. Lipolysis in white adipose tissues (WAT) and lipolysis-induced blood glucose rise were increased in Insr(P1195L/+)/HFD mice, while wild-type WAT transplantation ameliorated the hyperglycemia and the increased G6pc expression. We found that the expressions of genes involved in bile acid (BA) metabolism were altered in Insr(P1195L/+)/HFD liver. Among these, the expression of Cyp7a1, a BA synthesis enzyme, was insulin-dependent and was markedly decreased in Insr(P1195L/+)/HFD liver. Reduced Cyp7a1 expression in Insr(P1195L/+)/HFD liver was rescued by WAT transplantation, and the expression of Cyp7a1 was suppressed by glycerol administration in wild-type liver. These findings suggest that unsuppressed lipolysis in adipocytes elicited by HFD feeding is linked with enhanced gluconeogenesis from glycerol and with alterations in BA physiology in Insr(P1195L/+)/HFD liver. Nature Publishing Group 2015-11-30 /pmc/articles/PMC4663474/ /pubmed/26615883 http://dx.doi.org/10.1038/srep17565 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Lee, Eun Young
Sakurai, Kenichi
Zhang, Xilin
Toda, Chitoku
Tanaka, Tomoaki
Jiang, Meizi
Shirasawa, Takuji
Tachibana, Kaori
Yokote, Koutaro
Vidal-Puig, Antonio
Minokoshi, Yasuhiko
Miki, Takashi
Unsuppressed lipolysis in adipocytes is linked with enhanced gluconeogenesis and altered bile acid physiology in Insr(P1195L/+) mice fed high-fat-diet
title Unsuppressed lipolysis in adipocytes is linked with enhanced gluconeogenesis and altered bile acid physiology in Insr(P1195L/+) mice fed high-fat-diet
title_full Unsuppressed lipolysis in adipocytes is linked with enhanced gluconeogenesis and altered bile acid physiology in Insr(P1195L/+) mice fed high-fat-diet
title_fullStr Unsuppressed lipolysis in adipocytes is linked with enhanced gluconeogenesis and altered bile acid physiology in Insr(P1195L/+) mice fed high-fat-diet
title_full_unstemmed Unsuppressed lipolysis in adipocytes is linked with enhanced gluconeogenesis and altered bile acid physiology in Insr(P1195L/+) mice fed high-fat-diet
title_short Unsuppressed lipolysis in adipocytes is linked with enhanced gluconeogenesis and altered bile acid physiology in Insr(P1195L/+) mice fed high-fat-diet
title_sort unsuppressed lipolysis in adipocytes is linked with enhanced gluconeogenesis and altered bile acid physiology in insr(p1195l/+) mice fed high-fat-diet
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4663474/
https://www.ncbi.nlm.nih.gov/pubmed/26615883
http://dx.doi.org/10.1038/srep17565
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