DPP-4 inhibitors improve cognition and brain mitochondrial function of insulin-resistant rats

Recent evidence has demonstrated that insulin resistance is related to the development of type 2 diabetes mellitus. Our previous study found that high-fat diet (HFD) consumption caused not only peripheral and brain insulin resistance but also brain mitochondrial dysfunction and cognitive impairment....

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Main Authors: Pintana H., Apaijai N., Chattipakorn N., Chattipakorn S.C.
Format: Article
Language:English
Published: 2014
Online Access:http://www.scopus.com/inward/record.url?eid=2-s2.0-84878781836&partnerID=40&md5=2891413de129d193fc50d23104a00173
http://cmuir.cmu.ac.th/handle/6653943832/4163
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Institution: Chiang Mai University
Language: English
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spelling th-cmuir.6653943832-41632014-08-30T02:35:44Z DPP-4 inhibitors improve cognition and brain mitochondrial function of insulin-resistant rats Pintana H. Apaijai N. Chattipakorn N. Chattipakorn S.C. Recent evidence has demonstrated that insulin resistance is related to the development of type 2 diabetes mellitus. Our previous study found that high-fat diet (HFD) consumption caused not only peripheral and brain insulin resistance but also brain mitochondrial dysfunction and cognitive impairment. Vildagliptin and sitagliptin, dipeptidyl-peptidase-4 inhibitors, are recently developed anti-diabetic drugs. However, the effects of both drugs on cognitive behaviors and brain mitochondrial function in HFD-induced insulin-resistant rats have not yet been investigated. Sixty male Wistar rats were divided into two groups to receive either normal diet or HFD for 12 weeks. Rats in each group were then further divided into three treatment groups to receive either vehicle, vildagliptin (3 mg/kg per day), or sitagliptin (30 mg/kg per day) for 21 days. The cognitive behaviors of the rats were tested using the Morris Water Maze test. Blood samples were collected to determine metabolic parameters and plasma oxidative stress levels. Upon completion of the study, the animals were killed and the brains were removed to investigate brain and hippocampal mitochondrial function as well as to determine oxidative stress levels.We demonstrated that both drugs significantly improved the metabolic parameters and decreased circulating and brain oxidative stress levels in HFD-induced insulin-resistant rats. In addition, both drugs completely prevented brain and hippocampal mitochondrial dysfunction and equally improved the learning behaviors impaired by the HFD. Our findings suggest that the inhibition of dipeptidyl-peptidase-4 enzymes with vildagliptin or sitagliptin in insulinresistant rats not only increases peripheral insulin sensitivity but also decreases brain dysfunction. © 2013 Society for Endocrinology. 2014-08-30T02:35:44Z 2014-08-30T02:35:44Z 2013 Article 00220795 10.1530/JOE-12-0521 23591914 JOENA http://www.scopus.com/inward/record.url?eid=2-s2.0-84878781836&partnerID=40&md5=2891413de129d193fc50d23104a00173 http://cmuir.cmu.ac.th/handle/6653943832/4163 English
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description Recent evidence has demonstrated that insulin resistance is related to the development of type 2 diabetes mellitus. Our previous study found that high-fat diet (HFD) consumption caused not only peripheral and brain insulin resistance but also brain mitochondrial dysfunction and cognitive impairment. Vildagliptin and sitagliptin, dipeptidyl-peptidase-4 inhibitors, are recently developed anti-diabetic drugs. However, the effects of both drugs on cognitive behaviors and brain mitochondrial function in HFD-induced insulin-resistant rats have not yet been investigated. Sixty male Wistar rats were divided into two groups to receive either normal diet or HFD for 12 weeks. Rats in each group were then further divided into three treatment groups to receive either vehicle, vildagliptin (3 mg/kg per day), or sitagliptin (30 mg/kg per day) for 21 days. The cognitive behaviors of the rats were tested using the Morris Water Maze test. Blood samples were collected to determine metabolic parameters and plasma oxidative stress levels. Upon completion of the study, the animals were killed and the brains were removed to investigate brain and hippocampal mitochondrial function as well as to determine oxidative stress levels.We demonstrated that both drugs significantly improved the metabolic parameters and decreased circulating and brain oxidative stress levels in HFD-induced insulin-resistant rats. In addition, both drugs completely prevented brain and hippocampal mitochondrial dysfunction and equally improved the learning behaviors impaired by the HFD. Our findings suggest that the inhibition of dipeptidyl-peptidase-4 enzymes with vildagliptin or sitagliptin in insulinresistant rats not only increases peripheral insulin sensitivity but also decreases brain dysfunction. © 2013 Society for Endocrinology.
format Article
author Pintana H.
Apaijai N.
Chattipakorn N.
Chattipakorn S.C.
spellingShingle Pintana H.
Apaijai N.
Chattipakorn N.
Chattipakorn S.C.
DPP-4 inhibitors improve cognition and brain mitochondrial function of insulin-resistant rats
author_facet Pintana H.
Apaijai N.
Chattipakorn N.
Chattipakorn S.C.
author_sort Pintana H.
title DPP-4 inhibitors improve cognition and brain mitochondrial function of insulin-resistant rats
title_short DPP-4 inhibitors improve cognition and brain mitochondrial function of insulin-resistant rats
title_full DPP-4 inhibitors improve cognition and brain mitochondrial function of insulin-resistant rats
title_fullStr DPP-4 inhibitors improve cognition and brain mitochondrial function of insulin-resistant rats
title_full_unstemmed DPP-4 inhibitors improve cognition and brain mitochondrial function of insulin-resistant rats
title_sort dpp-4 inhibitors improve cognition and brain mitochondrial function of insulin-resistant rats
publishDate 2014
url http://www.scopus.com/inward/record.url?eid=2-s2.0-84878781836&partnerID=40&md5=2891413de129d193fc50d23104a00173
http://cmuir.cmu.ac.th/handle/6653943832/4163
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