Calorie restriction prevents the development of insulin resistance and impaired insulin signaling in skeletal muscle of ovariectomized rats

Insulin resistance of skeletal muscle glucose transport due to prolonged loss of ovarian function in ovariectomized (OVX) rats is accompanied by other features of the metabolic syndrome and may be confounded by increased calorie consumption. In this study, we investigated the role of calorie consump...

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Main Authors: Prasannarong,M., Vichaiwong,K., Saengsirisuwan,V.
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Published: Elsevier 2015
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spelling th-cmuir.6653943832-380992015-06-16T07:38:24Z Calorie restriction prevents the development of insulin resistance and impaired insulin signaling in skeletal muscle of ovariectomized rats Prasannarong,M. Vichaiwong,K. Saengsirisuwan,V. Molecular Medicine Molecular Biology Insulin resistance of skeletal muscle glucose transport due to prolonged loss of ovarian function in ovariectomized (OVX) rats is accompanied by other features of the metabolic syndrome and may be confounded by increased calorie consumption. In this study, we investigated the role of calorie consumption in the development of insulin resistance in OVX rats. In addition, we examined the cellular mechanisms underlying skeletal muscle insulin resistance in OVX rats. Female Sprague-Dawley rats were ovariectomized (OVX) or sham-operated (SHAM). OVX rats either had free access to food, pair feeding (PF) with SHAM or received a 35% reduction in food intake (calorie restriction; CR) for 12weeks. Compared with SHAM, ovariectomy induced skeletal muscle insulin resistance, which was associated with decreases (32-70%) in tyrosine phosphorylation of the insulin receptor and insulin receptor substrate-1 (IRS-1), IRS-1 associated p85 subunit of phosphatidylinositol 3-kinase (PI3-kinase), and Akt Ser 473 phosphorylation whereas insulin-stimulated phosphorylation of IRS-1 Ser 307, SAPK/JNK Thr 183/Tyr 185, and p38 mitogen-activated protein kinase (MAPK) Thr 180/Tyr 182 was increased (24-62%). PF improved the serum lipid profile but did not restore insulin-stimulated glucose transport, indicating that insulin resistance in OVX rats is a consequence of ovarian hormone deprivation. In contrast, impaired insulin sensitivity and defective insulin signaling were not observed in the skeletal muscle of OVX+CR rats. Therefore, we provide evidence for the first time that CR effectively prevents the development of insulin resistance and impaired insulin signaling in the skeletal muscle of OVX rats. © 2012 Elsevier B.V. 2015-06-16T07:38:24Z 2015-06-16T07:38:24Z 2012-06-01 Article 09254439 2-s2.0-84859056344 10.1016/j.bbadis.2012.02.018 22406051 http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84859056344&origin=inward http://cmuir.cmu.ac.th/handle/6653943832/38099 Elsevier
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Molecular Medicine
Molecular Biology
spellingShingle Molecular Medicine
Molecular Biology
Prasannarong,M.
Vichaiwong,K.
Saengsirisuwan,V.
Calorie restriction prevents the development of insulin resistance and impaired insulin signaling in skeletal muscle of ovariectomized rats
description Insulin resistance of skeletal muscle glucose transport due to prolonged loss of ovarian function in ovariectomized (OVX) rats is accompanied by other features of the metabolic syndrome and may be confounded by increased calorie consumption. In this study, we investigated the role of calorie consumption in the development of insulin resistance in OVX rats. In addition, we examined the cellular mechanisms underlying skeletal muscle insulin resistance in OVX rats. Female Sprague-Dawley rats were ovariectomized (OVX) or sham-operated (SHAM). OVX rats either had free access to food, pair feeding (PF) with SHAM or received a 35% reduction in food intake (calorie restriction; CR) for 12weeks. Compared with SHAM, ovariectomy induced skeletal muscle insulin resistance, which was associated with decreases (32-70%) in tyrosine phosphorylation of the insulin receptor and insulin receptor substrate-1 (IRS-1), IRS-1 associated p85 subunit of phosphatidylinositol 3-kinase (PI3-kinase), and Akt Ser 473 phosphorylation whereas insulin-stimulated phosphorylation of IRS-1 Ser 307, SAPK/JNK Thr 183/Tyr 185, and p38 mitogen-activated protein kinase (MAPK) Thr 180/Tyr 182 was increased (24-62%). PF improved the serum lipid profile but did not restore insulin-stimulated glucose transport, indicating that insulin resistance in OVX rats is a consequence of ovarian hormone deprivation. In contrast, impaired insulin sensitivity and defective insulin signaling were not observed in the skeletal muscle of OVX+CR rats. Therefore, we provide evidence for the first time that CR effectively prevents the development of insulin resistance and impaired insulin signaling in the skeletal muscle of OVX rats. © 2012 Elsevier B.V.
format Article
author Prasannarong,M.
Vichaiwong,K.
Saengsirisuwan,V.
author_facet Prasannarong,M.
Vichaiwong,K.
Saengsirisuwan,V.
author_sort Prasannarong,M.
title Calorie restriction prevents the development of insulin resistance and impaired insulin signaling in skeletal muscle of ovariectomized rats
title_short Calorie restriction prevents the development of insulin resistance and impaired insulin signaling in skeletal muscle of ovariectomized rats
title_full Calorie restriction prevents the development of insulin resistance and impaired insulin signaling in skeletal muscle of ovariectomized rats
title_fullStr Calorie restriction prevents the development of insulin resistance and impaired insulin signaling in skeletal muscle of ovariectomized rats
title_full_unstemmed Calorie restriction prevents the development of insulin resistance and impaired insulin signaling in skeletal muscle of ovariectomized rats
title_sort calorie restriction prevents the development of insulin resistance and impaired insulin signaling in skeletal muscle of ovariectomized rats
publisher Elsevier
publishDate 2015
url http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84859056344&origin=inward
http://cmuir.cmu.ac.th/handle/6653943832/38099
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