Vildagliptin and caloric restriction for cardioprotection in pre-diabetic rats

© 2017 Society for Endocrinology. Long-term high-fat diet (HFD) consumption causes cardiac dysfunction. Although calorie restriction (CR) has been shown to be useful in obesity, we hypothesized that combined CR with dipeptidyl peptidase-4 (DPP-4) inhibitor provides greater efficacy than monotherapy...

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Main Authors: Pongpan Tanajak, Hiranya Pintana, Natthaphat Siri-Angkul, Juthamas Khamseekaew, Nattayaporn Apaijai, Siriporn C. Chattipakorn, Nipon Chattipakorn
Format: Journal
Published: 2018
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http://cmuir.cmu.ac.th/jspui/handle/6653943832/56814
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spelling th-cmuir.6653943832-568142018-09-05T03:49:49Z Vildagliptin and caloric restriction for cardioprotection in pre-diabetic rats Pongpan Tanajak Hiranya Pintana Natthaphat Siri-Angkul Juthamas Khamseekaew Nattayaporn Apaijai Siriporn C. Chattipakorn Nipon Chattipakorn Biochemistry, Genetics and Molecular Biology Medicine © 2017 Society for Endocrinology. Long-term high-fat diet (HFD) consumption causes cardiac dysfunction. Although calorie restriction (CR) has been shown to be useful in obesity, we hypothesized that combined CR with dipeptidyl peptidase-4 (DPP-4) inhibitor provides greater efficacy than monotherapy in attenuating cardiac dysfunction and metabolic impairment in HFDinduced obese-insulin resistant rats. Thirty male Wistar rats were divided into 2 groups to be fed on either a normal diet (ND, n = 6) or a HFD (n = 24) for 12 weeks. Then, HFD rats were divided into 4 subgroups (n = 6/subgroup) to receive just the vehicle, CR diet (60% of mean energy intake and changed to ND), vildagliptin (3 mg/kg/day) or combined CR and vildagliptin for 4 weeks. Metabolic parameters, heart rate variability (HRV), cardiac mitochondrial function, left ventricular (LV) and fibroblast growth factor (FGF) 21 signaling pathway were determined. Rats on a HFD developed insulin and FGF21 resistance, oxidative stress, cardiac mitochondrial dysfunction and impaired LV function. Rats on CR alone showed both decreased body weight and visceral fat accumulation, whereas vildagliptin did not alter these parameters. Rats in CR, vildagliptin and CR plus vildagliptin subgroups had improved insulin sensitivity and oxidative stress. However, vildagliptin improved heart rate variability (HRV), cardiac mitochondrial function and LV function better than the CR. Chronic HFD consumption leads to obese-insulin resistance and FGF21 resistance. Although CR is effective in improving metabolic regulation, vildagliptin provides greater efficacy in preventing cardiac dysfunction by improving anti-apoptosis and FGF21 signaling pathways and attenuating cardiac mitochondrial dysfunction in obese-insulin-resistant rats. 2018-09-05T03:30:35Z 2018-09-05T03:30:35Z 2017-01-01 Journal 14796805 00220795 2-s2.0-85011977227 10.1530/JOE-16-0406 https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85011977227&origin=inward http://cmuir.cmu.ac.th/jspui/handle/6653943832/56814
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
topic Biochemistry, Genetics and Molecular Biology
Medicine
spellingShingle Biochemistry, Genetics and Molecular Biology
Medicine
Pongpan Tanajak
Hiranya Pintana
Natthaphat Siri-Angkul
Juthamas Khamseekaew
Nattayaporn Apaijai
Siriporn C. Chattipakorn
Nipon Chattipakorn
Vildagliptin and caloric restriction for cardioprotection in pre-diabetic rats
description © 2017 Society for Endocrinology. Long-term high-fat diet (HFD) consumption causes cardiac dysfunction. Although calorie restriction (CR) has been shown to be useful in obesity, we hypothesized that combined CR with dipeptidyl peptidase-4 (DPP-4) inhibitor provides greater efficacy than monotherapy in attenuating cardiac dysfunction and metabolic impairment in HFDinduced obese-insulin resistant rats. Thirty male Wistar rats were divided into 2 groups to be fed on either a normal diet (ND, n = 6) or a HFD (n = 24) for 12 weeks. Then, HFD rats were divided into 4 subgroups (n = 6/subgroup) to receive just the vehicle, CR diet (60% of mean energy intake and changed to ND), vildagliptin (3 mg/kg/day) or combined CR and vildagliptin for 4 weeks. Metabolic parameters, heart rate variability (HRV), cardiac mitochondrial function, left ventricular (LV) and fibroblast growth factor (FGF) 21 signaling pathway were determined. Rats on a HFD developed insulin and FGF21 resistance, oxidative stress, cardiac mitochondrial dysfunction and impaired LV function. Rats on CR alone showed both decreased body weight and visceral fat accumulation, whereas vildagliptin did not alter these parameters. Rats in CR, vildagliptin and CR plus vildagliptin subgroups had improved insulin sensitivity and oxidative stress. However, vildagliptin improved heart rate variability (HRV), cardiac mitochondrial function and LV function better than the CR. Chronic HFD consumption leads to obese-insulin resistance and FGF21 resistance. Although CR is effective in improving metabolic regulation, vildagliptin provides greater efficacy in preventing cardiac dysfunction by improving anti-apoptosis and FGF21 signaling pathways and attenuating cardiac mitochondrial dysfunction in obese-insulin-resistant rats.
format Journal
author Pongpan Tanajak
Hiranya Pintana
Natthaphat Siri-Angkul
Juthamas Khamseekaew
Nattayaporn Apaijai
Siriporn C. Chattipakorn
Nipon Chattipakorn
author_facet Pongpan Tanajak
Hiranya Pintana
Natthaphat Siri-Angkul
Juthamas Khamseekaew
Nattayaporn Apaijai
Siriporn C. Chattipakorn
Nipon Chattipakorn
author_sort Pongpan Tanajak
title Vildagliptin and caloric restriction for cardioprotection in pre-diabetic rats
title_short Vildagliptin and caloric restriction for cardioprotection in pre-diabetic rats
title_full Vildagliptin and caloric restriction for cardioprotection in pre-diabetic rats
title_fullStr Vildagliptin and caloric restriction for cardioprotection in pre-diabetic rats
title_full_unstemmed Vildagliptin and caloric restriction for cardioprotection in pre-diabetic rats
title_sort vildagliptin and caloric restriction for cardioprotection in pre-diabetic rats
publishDate 2018
url https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85011977227&origin=inward
http://cmuir.cmu.ac.th/jspui/handle/6653943832/56814
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