Alpha-Lipoic Acid Regulates Lipid Metabolism through Induction of SIRT1 and Activation of AMP-Activated Protein Kinase

博士 === 臺北醫學大學 === 醫學科學研究所 === 100 === Obesity and diseases associated with obesity such as dyslipidemia, fatty liver, non-alcoholic steatotic hepatitis, and metabolic syndrome are increasingly important causes of morbidity and mortality in the general population worldwide.  Sirtuin 1 (SIRT1) is a...

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Main Authors: Weu-Lu Chen, 陳韋陸
Other Authors: Horng-Mo Lee
Format: Others
Language:zh-TW
Published: 2011
Online Access:http://ndltd.ncl.edu.tw/handle/83699811242337545521
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spelling ndltd-TW-100TMC055340062015-10-13T22:07:38Z http://ndltd.ncl.edu.tw/handle/83699811242337545521 Alpha-Lipoic Acid Regulates Lipid Metabolism through Induction of SIRT1 and Activation of AMP-Activated Protein Kinase 硫辛酸透過SIRT1及AMPK蛋白對脂肪代謝的調控 Weu-Lu Chen 陳韋陸 博士 臺北醫學大學 醫學科學研究所 100 Obesity and diseases associated with obesity such as dyslipidemia, fatty liver, non-alcoholic steatotic hepatitis, and metabolic syndrome are increasingly important causes of morbidity and mortality in the general population worldwide.  Sirtuin 1 (SIRT1) is a longevity-associated protein, which regulates energy metabolism and lifespan in response to nutrient deprivation. SIRT1 was proposed to be a therapeutic target for obesity and metabolic syndrome. Alpha-lipoic acid (ALA) is a powerful antioxidant, which has been shown to decrease hypothalamic AMPK and thus appetite, and exerts anti-obesity effects. More importantly, ALA activates AMPK signaling pathway in a variety of cells. In the present study, we investigated whether ALA exerts a lipid-lowering effect through regulation of SIRT1 activation and expression in C2C12 myotubes. ALA increased the NAD+-to-NADH ratio to enhance SIRT1 activity and expression in C2C12 myotubes. After deacetylation of LKB-1 by activated SIRT1, ALA increased AMPK and ACC phosphorylation, which increased palmitate β-oxidation in C2C12 myotubes. Treatment of cells with nicotinamide, or transfection with SIRT1 siRNA reduced ALA-mediated AMPK/ACC phosphorylation and palmitate β-oxidation suggesting that SIRT1 is an upstream regulator of AMPK. ALA increased ATGL and suppressed FAS protein expressions, leading to a decrease of intracellular triacylglycerol accumulation in C2C12 myotubes. Oral administration of ALA in type 2 diabetic mice fed a high-fat diet and db/db mice dramatically reduced the body weight and visceral fat content. ALA activates both SIRT1 and AMPK and leads to lipid lowering effects in vitro and in vivo. These findings suggest that ALA may exert beneficial effects in the treatment of dyslipidemia and obesity. Horng-Mo Lee 李宏謨 2011 學位論文 ; thesis 103 zh-TW
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description 博士 === 臺北醫學大學 === 醫學科學研究所 === 100 === Obesity and diseases associated with obesity such as dyslipidemia, fatty liver, non-alcoholic steatotic hepatitis, and metabolic syndrome are increasingly important causes of morbidity and mortality in the general population worldwide.  Sirtuin 1 (SIRT1) is a longevity-associated protein, which regulates energy metabolism and lifespan in response to nutrient deprivation. SIRT1 was proposed to be a therapeutic target for obesity and metabolic syndrome. Alpha-lipoic acid (ALA) is a powerful antioxidant, which has been shown to decrease hypothalamic AMPK and thus appetite, and exerts anti-obesity effects. More importantly, ALA activates AMPK signaling pathway in a variety of cells. In the present study, we investigated whether ALA exerts a lipid-lowering effect through regulation of SIRT1 activation and expression in C2C12 myotubes. ALA increased the NAD+-to-NADH ratio to enhance SIRT1 activity and expression in C2C12 myotubes. After deacetylation of LKB-1 by activated SIRT1, ALA increased AMPK and ACC phosphorylation, which increased palmitate β-oxidation in C2C12 myotubes. Treatment of cells with nicotinamide, or transfection with SIRT1 siRNA reduced ALA-mediated AMPK/ACC phosphorylation and palmitate β-oxidation suggesting that SIRT1 is an upstream regulator of AMPK. ALA increased ATGL and suppressed FAS protein expressions, leading to a decrease of intracellular triacylglycerol accumulation in C2C12 myotubes. Oral administration of ALA in type 2 diabetic mice fed a high-fat diet and db/db mice dramatically reduced the body weight and visceral fat content. ALA activates both SIRT1 and AMPK and leads to lipid lowering effects in vitro and in vivo. These findings suggest that ALA may exert beneficial effects in the treatment of dyslipidemia and obesity.
author2 Horng-Mo Lee
author_facet Horng-Mo Lee
Weu-Lu Chen
陳韋陸
author Weu-Lu Chen
陳韋陸
spellingShingle Weu-Lu Chen
陳韋陸
Alpha-Lipoic Acid Regulates Lipid Metabolism through Induction of SIRT1 and Activation of AMP-Activated Protein Kinase
author_sort Weu-Lu Chen
title Alpha-Lipoic Acid Regulates Lipid Metabolism through Induction of SIRT1 and Activation of AMP-Activated Protein Kinase
title_short Alpha-Lipoic Acid Regulates Lipid Metabolism through Induction of SIRT1 and Activation of AMP-Activated Protein Kinase
title_full Alpha-Lipoic Acid Regulates Lipid Metabolism through Induction of SIRT1 and Activation of AMP-Activated Protein Kinase
title_fullStr Alpha-Lipoic Acid Regulates Lipid Metabolism through Induction of SIRT1 and Activation of AMP-Activated Protein Kinase
title_full_unstemmed Alpha-Lipoic Acid Regulates Lipid Metabolism through Induction of SIRT1 and Activation of AMP-Activated Protein Kinase
title_sort alpha-lipoic acid regulates lipid metabolism through induction of sirt1 and activation of amp-activated protein kinase
publishDate 2011
url http://ndltd.ncl.edu.tw/handle/83699811242337545521
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