Cardioprotective effects of metformin and vildagliptin in adult rats with insulin resistance induced by a high-fat diet
Insulin resistance has been shown to be associated with cardiac sympathovagal imbalance, myocardial dysfunction, and cardiac mitochondrial dysfunction. Whereas metformin is a widely used antidiabetic drug to improve insulin resistance, vildagliptin is a novel oral antidiabetic drug in a group of dip...
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th-cmuir.6653943832-513662018-09-04T06:00:50Z Cardioprotective effects of metformin and vildagliptin in adult rats with insulin resistance induced by a high-fat diet Nattayaporn Apaijai Hiranya Pintana Siriporn C. Chattipakorn Nipon Chattipakorn Biochemistry, Genetics and Molecular Biology Insulin resistance has been shown to be associated with cardiac sympathovagal imbalance, myocardial dysfunction, and cardiac mitochondrial dysfunction. Whereas metformin is a widely used antidiabetic drug to improve insulin resistance, vildagliptin is a novel oral antidiabetic drug in a group of dipeptidyl peptidase-4 inhibitors in which its cardiac effect is unclear. This study aimed to determine the cardiovascular effects of metformin and vildagliptin in rats with insulin resistance induced by high-fat diet. Male Wistar rats were fed with either a normal diet or high-fat diet (n=24 each) for 12 wk. Rats in each group were divided into three subgroups to receive the vehicle, metformin (30 mg/kg, twice daily), or vildagliptin (3 mg/kg, once daily) for another 21 d. Heart rate variability (HRV), cardiac function, and cardiac mitochondrial function were determined and compared among these treatment groups. Rats exposed to a high-fat diet developed increased body weight, visceral fat, plasma insulin, cholesterol, oxidative stress, depressed HRV, and cardiac mitochondrial dysfunction. Metformin and vildagliptin did not alter body weight and plasma glucose levels but decreased the plasma insulin, total cholesterol, and oxidative stress levels. Although both metformin and vildagliptin attenuated the depressed HRV, cardiac dysfunction, and cardiac mitochondrial dysfunction, vildagliptin was more effective in this prevention. Furthermore, only vildagliptin prevented cardiac mitochondrial membrane depolarization caused by consumption of a high-fat diet. We concluded that vildagliptin is more effective in preventing cardiac sympathovagal imbalance and cardiac dysfunction, as well as cardiac mitochondrial dysfunction, than metformin in rats with insulin resistance induced by high-fat diet. Copyright © 2012 by The Endocrine Society. 2018-09-04T06:00:50Z 2018-09-04T06:00:50Z 2012-08-01 Journal 19457170 00137227 2-s2.0-84864382843 10.1210/en.2012-1262 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84864382843&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/51366 |
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Biochemistry, Genetics and Molecular Biology Nattayaporn Apaijai Hiranya Pintana Siriporn C. Chattipakorn Nipon Chattipakorn Cardioprotective effects of metformin and vildagliptin in adult rats with insulin resistance induced by a high-fat diet |
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Insulin resistance has been shown to be associated with cardiac sympathovagal imbalance, myocardial dysfunction, and cardiac mitochondrial dysfunction. Whereas metformin is a widely used antidiabetic drug to improve insulin resistance, vildagliptin is a novel oral antidiabetic drug in a group of dipeptidyl peptidase-4 inhibitors in which its cardiac effect is unclear. This study aimed to determine the cardiovascular effects of metformin and vildagliptin in rats with insulin resistance induced by high-fat diet. Male Wistar rats were fed with either a normal diet or high-fat diet (n=24 each) for 12 wk. Rats in each group were divided into three subgroups to receive the vehicle, metformin (30 mg/kg, twice daily), or vildagliptin (3 mg/kg, once daily) for another 21 d. Heart rate variability (HRV), cardiac function, and cardiac mitochondrial function were determined and compared among these treatment groups. Rats exposed to a high-fat diet developed increased body weight, visceral fat, plasma insulin, cholesterol, oxidative stress, depressed HRV, and cardiac mitochondrial dysfunction. Metformin and vildagliptin did not alter body weight and plasma glucose levels but decreased the plasma insulin, total cholesterol, and oxidative stress levels. Although both metformin and vildagliptin attenuated the depressed HRV, cardiac dysfunction, and cardiac mitochondrial dysfunction, vildagliptin was more effective in this prevention. Furthermore, only vildagliptin prevented cardiac mitochondrial membrane depolarization caused by consumption of a high-fat diet. We concluded that vildagliptin is more effective in preventing cardiac sympathovagal imbalance and cardiac dysfunction, as well as cardiac mitochondrial dysfunction, than metformin in rats with insulin resistance induced by high-fat diet. Copyright © 2012 by The Endocrine Society. |
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Nattayaporn Apaijai Hiranya Pintana Siriporn C. Chattipakorn Nipon Chattipakorn |
author_facet |
Nattayaporn Apaijai Hiranya Pintana Siriporn C. Chattipakorn Nipon Chattipakorn |
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Nattayaporn Apaijai |
title |
Cardioprotective effects of metformin and vildagliptin in adult rats with insulin resistance induced by a high-fat diet |
title_short |
Cardioprotective effects of metformin and vildagliptin in adult rats with insulin resistance induced by a high-fat diet |
title_full |
Cardioprotective effects of metformin and vildagliptin in adult rats with insulin resistance induced by a high-fat diet |
title_fullStr |
Cardioprotective effects of metformin and vildagliptin in adult rats with insulin resistance induced by a high-fat diet |
title_full_unstemmed |
Cardioprotective effects of metformin and vildagliptin in adult rats with insulin resistance induced by a high-fat diet |
title_sort |
cardioprotective effects of metformin and vildagliptin in adult rats with insulin resistance induced by a high-fat diet |
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2018 |
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https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84864382843&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/51366 |
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