Literature DB >> 20651844

Calorie restriction on insulin resistance and expression of SIRT1 and SIRT4 in rats.

Yong-Ru Chen1, Shi-Rong Fang, Yu-Cai Fu, Xiao-Hui Zhou, Ming-Yan Xu, Wen-Can Xu.   

Abstract

The sirtuin proteins are nicotinamide adenine dinucleotide dependent deacetylases and adenosine diphosphate (ADP)-ribosyl transferases associated with metabolic balance and lifespan extension. Sirtuin 1 (SIRT1) and sirtuin 4 (SIRT4) have been reported to regulate insulin secretion, but their association with the development of insulin resistance and nonalcoholic fatty liver disease remain undefined. The aim of this study was to determine the expression of SIRT1 and SIRT4 in the liver and pancreas of rats fed with different diets and analyze the association of these proteins with insulin resistance and nonalcoholic fatty liver disease. Male Sprague-Dawley rats were randomly divided into the following 4 diet treatment groups: normal control (NC), calorie restriction (CR), high-fat (HFa), and high-fructose (HFr), and these groups were maintained for 12 weeks. Blood biochemical analysis and histopathology indicated that HFa and HFr groups were insulin resistant and developed nonalcoholic fatty livers. SIRT1 was present in the nucleus and cytoplasm of the pancreatic beta-cells, while SIRT4 was located in the cytoplasm. Treatment with the CR diet increased the expression of SIRT1 in both the pancreas and liver, while treatment with the HFa and HFr diets caused a decrease. SIRT4 was upregulated in the liver of rats treated with the HFa diet, but did not change with the CR diet treatment. These data suggest that SIRT1 and SIRT4 were both involved in the development of insulin resistance and nonalcoholic fatty liver disease.

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Year:  2010        PMID: 20651844     DOI: 10.1139/O10-010

Source DB:  PubMed          Journal:  Biochem Cell Biol        ISSN: 0829-8211            Impact factor:   3.626


  26 in total

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Review 4.  Translating cell survival and cell longevity into treatment strategies with SIRT1.

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5.  SIRT1 interacts with metabolic transcriptional factors in the pancreas of insulin-resistant and calorie-restricted rats.

Authors:  Yong-Ru Chen; Yu-Lin Lai; Shao-da Lin; Xi-Tao Li; Yu-Cai Fu; Wen-Can Xu
Journal:  Mol Biol Rep       Date:  2013-01-06       Impact factor: 2.316

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8.  Resveratrol enhances exercise training responses in rats selectively bred for high running performance.

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Review 10.  Signaling molecules involved in lipid-induced pancreatic beta-cell dysfunction.

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