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Telmisartan is effective to ameliorate metabolic syndrome in rat model – a preclinical report
BACKGROUND: Metabolic syndrome (MS) is known to be associated with hypertension, insulin resistance, and dyslipidemia, and it raises the risk for cardiovascular diseases and diabetes mellitus. Telmisartan is used in clinic as an angiotensin II receptor blocker and it is also identified as activating...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6290862/ https://www.ncbi.nlm.nih.gov/pubmed/30584345 http://dx.doi.org/10.2147/DMSO.S187092 |
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author | Cheng, Kai-Chun Li, Yingxiao Chang, Wei-Ting Kuo, Feng Yu Chen, Zhih-Cherng Cheng, Juei-Tang |
author_facet | Cheng, Kai-Chun Li, Yingxiao Chang, Wei-Ting Kuo, Feng Yu Chen, Zhih-Cherng Cheng, Juei-Tang |
author_sort | Cheng, Kai-Chun |
collection | PubMed |
description | BACKGROUND: Metabolic syndrome (MS) is known to be associated with hypertension, insulin resistance, and dyslipidemia, and it raises the risk for cardiovascular diseases and diabetes mellitus. Telmisartan is used in clinic as an angiotensin II receptor blocker and it is also identified as activating peroxisome proliferator-activated receptors δ (PPARδ). Activation of PPARδ produced beneficial effects on fatty acid metabolism and glucose metabolism. This study aims to investigate the effects of telmisartan on the modulation of MS in rats fed a high-fat/high-sodium diet. METHODS: Rats were fed with a high-fat/high-sodium diet and received injections of streptozotocin at low dose to induce MS. Then, rats with MS were treated with telmisartan. The weight, glucose tolerance, and insulin sensitivity were measured. The lipid profiles were also obtained. The weights of retroperitoneal and epididymal fat pads were determined. The role of PPARδ in telmisartan treatment was identified in rats pretreated with the specific antagonist GSK0660. RESULTS: The results showed that telmisartan, but not losartan, significantly reduced plasma glucose and plasma insulin, and improved insulin resistance in rats with MS. Telmisartan also decreased blood pressure and lipids more significantly than losartan. Moreover, GSK0660 effectively reversed the effects of telmisartan in the MS rats. In the MS group, telmisartan activated PPARδ to enhance the levels of phosphorylated GLUT4 in muscle or the expression of phosphoenolpyruvate carboxykinase (PEPCK) in the liver, which was also abolished by GSK0660. Telmisartan is useful to ameliorate hypertension and insulin resistance in rats with MS. Telmisartan improves the insulin resistance through increased expression of GLUT4 and down-regulation of PEPCK via PPARδ-dependent mechanisms. CONCLUSION: Telmisartan has been proven to ameliorate MS, particularly in the prediabetes state. Therefore, telmisartan is suitable to develop for the management of MS in clinics. |
format | Online Article Text |
id | pubmed-6290862 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-62908622018-12-24 Telmisartan is effective to ameliorate metabolic syndrome in rat model – a preclinical report Cheng, Kai-Chun Li, Yingxiao Chang, Wei-Ting Kuo, Feng Yu Chen, Zhih-Cherng Cheng, Juei-Tang Diabetes Metab Syndr Obes Original Research BACKGROUND: Metabolic syndrome (MS) is known to be associated with hypertension, insulin resistance, and dyslipidemia, and it raises the risk for cardiovascular diseases and diabetes mellitus. Telmisartan is used in clinic as an angiotensin II receptor blocker and it is also identified as activating peroxisome proliferator-activated receptors δ (PPARδ). Activation of PPARδ produced beneficial effects on fatty acid metabolism and glucose metabolism. This study aims to investigate the effects of telmisartan on the modulation of MS in rats fed a high-fat/high-sodium diet. METHODS: Rats were fed with a high-fat/high-sodium diet and received injections of streptozotocin at low dose to induce MS. Then, rats with MS were treated with telmisartan. The weight, glucose tolerance, and insulin sensitivity were measured. The lipid profiles were also obtained. The weights of retroperitoneal and epididymal fat pads were determined. The role of PPARδ in telmisartan treatment was identified in rats pretreated with the specific antagonist GSK0660. RESULTS: The results showed that telmisartan, but not losartan, significantly reduced plasma glucose and plasma insulin, and improved insulin resistance in rats with MS. Telmisartan also decreased blood pressure and lipids more significantly than losartan. Moreover, GSK0660 effectively reversed the effects of telmisartan in the MS rats. In the MS group, telmisartan activated PPARδ to enhance the levels of phosphorylated GLUT4 in muscle or the expression of phosphoenolpyruvate carboxykinase (PEPCK) in the liver, which was also abolished by GSK0660. Telmisartan is useful to ameliorate hypertension and insulin resistance in rats with MS. Telmisartan improves the insulin resistance through increased expression of GLUT4 and down-regulation of PEPCK via PPARδ-dependent mechanisms. CONCLUSION: Telmisartan has been proven to ameliorate MS, particularly in the prediabetes state. Therefore, telmisartan is suitable to develop for the management of MS in clinics. Dove Medical Press 2018-12-07 /pmc/articles/PMC6290862/ /pubmed/30584345 http://dx.doi.org/10.2147/DMSO.S187092 Text en © 2018 Cheng et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. |
spellingShingle | Original Research Cheng, Kai-Chun Li, Yingxiao Chang, Wei-Ting Kuo, Feng Yu Chen, Zhih-Cherng Cheng, Juei-Tang Telmisartan is effective to ameliorate metabolic syndrome in rat model – a preclinical report |
title | Telmisartan is effective to ameliorate metabolic syndrome in rat model – a preclinical report |
title_full | Telmisartan is effective to ameliorate metabolic syndrome in rat model – a preclinical report |
title_fullStr | Telmisartan is effective to ameliorate metabolic syndrome in rat model – a preclinical report |
title_full_unstemmed | Telmisartan is effective to ameliorate metabolic syndrome in rat model – a preclinical report |
title_short | Telmisartan is effective to ameliorate metabolic syndrome in rat model – a preclinical report |
title_sort | telmisartan is effective to ameliorate metabolic syndrome in rat model – a preclinical report |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6290862/ https://www.ncbi.nlm.nih.gov/pubmed/30584345 http://dx.doi.org/10.2147/DMSO.S187092 |
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