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Distinct Time Course of the Decrease in Hepatic AMP-Activated Protein Kinase and Akt Phosphorylation in Mice Fed a High Fat Diet

AMP-activated protein kinase (AMPK) plays an important role in insulin resistance, which is characterized by the impairment of the insulin-Akt signaling pathway. However, the time course of the decrease in AMPK and Akt phosphorylation in the liver during the development of obesity and insulin resist...

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Autores principales: Shiwa, Mami, Yoneda, Masayasu, Okubo, Hirofumi, Ohno, Haruya, Kobuke, Kazuhiro, Monzen, Yuko, Kishimoto, Rui, Nakatsu, Yusuke, Asano, Tomoichiro, Kohno, Nobuoki
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534138/
https://www.ncbi.nlm.nih.gov/pubmed/26266809
http://dx.doi.org/10.1371/journal.pone.0135554
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author Shiwa, Mami
Yoneda, Masayasu
Okubo, Hirofumi
Ohno, Haruya
Kobuke, Kazuhiro
Monzen, Yuko
Kishimoto, Rui
Nakatsu, Yusuke
Asano, Tomoichiro
Kohno, Nobuoki
author_facet Shiwa, Mami
Yoneda, Masayasu
Okubo, Hirofumi
Ohno, Haruya
Kobuke, Kazuhiro
Monzen, Yuko
Kishimoto, Rui
Nakatsu, Yusuke
Asano, Tomoichiro
Kohno, Nobuoki
author_sort Shiwa, Mami
collection PubMed
description AMP-activated protein kinase (AMPK) plays an important role in insulin resistance, which is characterized by the impairment of the insulin-Akt signaling pathway. However, the time course of the decrease in AMPK and Akt phosphorylation in the liver during the development of obesity and insulin resistance caused by feeding a high fat diet (HFD) remains controversial. Moreover, it is unclear whether the impairment of AMPK and Akt signaling pathways is reversible when changing from a HFD to a standard diet (SD). Male ddY mice were fed the SD or HFD for 3 to 28 days, or fed the HFD for 14 days, followed by the SD for 14 days. We examined the time course of the expression and phosphorylation levels of AMPK and Akt in the liver by immunoblotting. After 3 days of feeding on the HFD, mice gained body weight, resulting in an increased oil red O staining, indicative of hepatic lipid accumulation, and significantly decreased AMPK phosphorylation, in comparison with mice fed the SD. After 14 days on the HFD, systemic insulin resistance occurred and Akt phosphorylation significantly decreased. Subsequently, a change from the HFD to SD for 3 days, after 14 days on the HFD, ameliorated the impairment of AMPK and Akt phosphorylation and systemic insulin resistance. Our findings indicate that AMPK phosphorylation decreases early upon feeding a HFD and emphasizes the importance of prompt lifestyle modification for decreasing the risk of developing diabetes.
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spelling pubmed-45341382015-08-24 Distinct Time Course of the Decrease in Hepatic AMP-Activated Protein Kinase and Akt Phosphorylation in Mice Fed a High Fat Diet Shiwa, Mami Yoneda, Masayasu Okubo, Hirofumi Ohno, Haruya Kobuke, Kazuhiro Monzen, Yuko Kishimoto, Rui Nakatsu, Yusuke Asano, Tomoichiro Kohno, Nobuoki PLoS One Research Article AMP-activated protein kinase (AMPK) plays an important role in insulin resistance, which is characterized by the impairment of the insulin-Akt signaling pathway. However, the time course of the decrease in AMPK and Akt phosphorylation in the liver during the development of obesity and insulin resistance caused by feeding a high fat diet (HFD) remains controversial. Moreover, it is unclear whether the impairment of AMPK and Akt signaling pathways is reversible when changing from a HFD to a standard diet (SD). Male ddY mice were fed the SD or HFD for 3 to 28 days, or fed the HFD for 14 days, followed by the SD for 14 days. We examined the time course of the expression and phosphorylation levels of AMPK and Akt in the liver by immunoblotting. After 3 days of feeding on the HFD, mice gained body weight, resulting in an increased oil red O staining, indicative of hepatic lipid accumulation, and significantly decreased AMPK phosphorylation, in comparison with mice fed the SD. After 14 days on the HFD, systemic insulin resistance occurred and Akt phosphorylation significantly decreased. Subsequently, a change from the HFD to SD for 3 days, after 14 days on the HFD, ameliorated the impairment of AMPK and Akt phosphorylation and systemic insulin resistance. Our findings indicate that AMPK phosphorylation decreases early upon feeding a HFD and emphasizes the importance of prompt lifestyle modification for decreasing the risk of developing diabetes. Public Library of Science 2015-08-12 /pmc/articles/PMC4534138/ /pubmed/26266809 http://dx.doi.org/10.1371/journal.pone.0135554 Text en © 2015 Shiwa et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Shiwa, Mami
Yoneda, Masayasu
Okubo, Hirofumi
Ohno, Haruya
Kobuke, Kazuhiro
Monzen, Yuko
Kishimoto, Rui
Nakatsu, Yusuke
Asano, Tomoichiro
Kohno, Nobuoki
Distinct Time Course of the Decrease in Hepatic AMP-Activated Protein Kinase and Akt Phosphorylation in Mice Fed a High Fat Diet
title Distinct Time Course of the Decrease in Hepatic AMP-Activated Protein Kinase and Akt Phosphorylation in Mice Fed a High Fat Diet
title_full Distinct Time Course of the Decrease in Hepatic AMP-Activated Protein Kinase and Akt Phosphorylation in Mice Fed a High Fat Diet
title_fullStr Distinct Time Course of the Decrease in Hepatic AMP-Activated Protein Kinase and Akt Phosphorylation in Mice Fed a High Fat Diet
title_full_unstemmed Distinct Time Course of the Decrease in Hepatic AMP-Activated Protein Kinase and Akt Phosphorylation in Mice Fed a High Fat Diet
title_short Distinct Time Course of the Decrease in Hepatic AMP-Activated Protein Kinase and Akt Phosphorylation in Mice Fed a High Fat Diet
title_sort distinct time course of the decrease in hepatic amp-activated protein kinase and akt phosphorylation in mice fed a high fat diet
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4534138/
https://www.ncbi.nlm.nih.gov/pubmed/26266809
http://dx.doi.org/10.1371/journal.pone.0135554
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