Telmisartan ameliorates hyperglycemia and metabolic profile in nonobese Cohen-Rosenthal diabetic hypertensive rats via peroxisome proliferator activator receptor-g activation

The importance of hypertension treatment has expanded beyond blood pressure management to include additional risk factors, mainly diabetes. It was considered of interest to test the effect of telmisartan, an angiotensin receptor 1 antagonist and peroxisome proliferator activator receptor-g partial a...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Metabolism, clinical and experimental clinical and experimental, 2010-08, Vol.59 (8), p.1200-1209
Hauptverfasser: Younis, Firas, Stern, Naftali, Limor, Rona, Oron, Yoram, Zangen, Sarah, Rosenthal, Talma
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 1209
container_issue 8
container_start_page 1200
container_title Metabolism, clinical and experimental
container_volume 59
creator Younis, Firas
Stern, Naftali
Limor, Rona
Oron, Yoram
Zangen, Sarah
Rosenthal, Talma
description The importance of hypertension treatment has expanded beyond blood pressure management to include additional risk factors, mainly diabetes. It was considered of interest to test the effect of telmisartan, an angiotensin receptor 1 antagonist and peroxisome proliferator activator receptor-g partial agonist, on Cohen-Rosenthal diabetic hypertensive nonobese (CRDH) rats, a unique model combining both pathologies. Its effect was examined on fat-derived and inflammatory agents in CRDH. To determine the extent of the drug's peroxisome proliferator activator receptor-g modulating beneficial metabolic actions, results were compared with those obtained with valsartan and rosiglitazone in CRDH and Cohen diabetic rat (CDR). Telmisartan and valsartan were given in drinking water at 3 and 12 mg/kg/d, whereas rosiglitazone (3 mg/kg/d) was given as food admixture for a period of 5 months. Blood pressure, glucose, insulin, adiponectin, leptin, and tumor necrosis factor a were examined. Telmisartan and valsartan significantly (P < .01) reduced blood pressure, whereas telmisartan and rosiglitazone considerably reduced blood glucose levels to normoglycemic levels (P < .01) in these 2 strains. Insulin levels were not affected by telmisartan and valsartan but were slightly reduced by rosiglitazone in CDR. In contrast to valsartan, adiponectin was significantly (60%, P < .01) increased by telmisartan in both CDR and CRDH, whereas rosiglitazone induced a 60% and 180% increase in CRDH and CDR animals, respectively, on day 30 of treatment. Co-treatment with GW9662 averted telmisartan-induced rise of adiponectin. Tumor necrosis factor a declined in telmisartan-treated rats, less so with rosiglitazone, but not valsartan. Telmisartan also induced downsizing of epididymal adipocytes compared with valsartan. Leptin levels were significantly increased by valsartan (P < .05) but reduced by telmisartan and rosiglitazone. The telmisartan-induced increase in adiponectin was most probably associated with a decrease in glucose and tumor necrosis factor a levels. Therefore, in addition to its hypotensive effect, telmisartan demonstrated beneficial thiazolidinedione-like effects.
doi_str_mv 10.1016/j.metabol.2009.11.013
format Article
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_754880413</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>754880413</sourcerecordid><originalsourceid>FETCH-proquest_miscellaneous_7548804133</originalsourceid><addsrcrecordid>eNqNz8FOwzAMBuAcQGIwHgHJN04tztq13XkCcUa7T27nrpnSpMTZxF6KZyRM487Jv-xfn2SlnjTmGnX1cshHjtR6my8QV7nWOeriRs0QF1WG5Wp5p-5FDohY1001U98btqMRCpEc0MjW-ECRBYbzxGFvzx2PhoDcDq6w6WAKvjeWwThw3vmWhWHtB3bZhxd2cSALO0Mtx1S-QJGdmBNDsgVOCUw7_2XEj_yrWdNzOvkA1EVzuqTAHU8pZPu_pfFurm57ssKP1_mgnt9eN-v3LCGfR5a4Tc90bC059kfZ1suyabDURfH_5g9Vh286</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>754880413</pqid></control><display><type>article</type><title>Telmisartan ameliorates hyperglycemia and metabolic profile in nonobese Cohen-Rosenthal diabetic hypertensive rats via peroxisome proliferator activator receptor-g activation</title><source>Elsevier ScienceDirect Journals Complete</source><creator>Younis, Firas ; Stern, Naftali ; Limor, Rona ; Oron, Yoram ; Zangen, Sarah ; Rosenthal, Talma</creator><creatorcontrib>Younis, Firas ; Stern, Naftali ; Limor, Rona ; Oron, Yoram ; Zangen, Sarah ; Rosenthal, Talma</creatorcontrib><description>The importance of hypertension treatment has expanded beyond blood pressure management to include additional risk factors, mainly diabetes. It was considered of interest to test the effect of telmisartan, an angiotensin receptor 1 antagonist and peroxisome proliferator activator receptor-g partial agonist, on Cohen-Rosenthal diabetic hypertensive nonobese (CRDH) rats, a unique model combining both pathologies. Its effect was examined on fat-derived and inflammatory agents in CRDH. To determine the extent of the drug's peroxisome proliferator activator receptor-g modulating beneficial metabolic actions, results were compared with those obtained with valsartan and rosiglitazone in CRDH and Cohen diabetic rat (CDR). Telmisartan and valsartan were given in drinking water at 3 and 12 mg/kg/d, whereas rosiglitazone (3 mg/kg/d) was given as food admixture for a period of 5 months. Blood pressure, glucose, insulin, adiponectin, leptin, and tumor necrosis factor a were examined. Telmisartan and valsartan significantly (P &lt; .01) reduced blood pressure, whereas telmisartan and rosiglitazone considerably reduced blood glucose levels to normoglycemic levels (P &lt; .01) in these 2 strains. Insulin levels were not affected by telmisartan and valsartan but were slightly reduced by rosiglitazone in CDR. In contrast to valsartan, adiponectin was significantly (60%, P &lt; .01) increased by telmisartan in both CDR and CRDH, whereas rosiglitazone induced a 60% and 180% increase in CRDH and CDR animals, respectively, on day 30 of treatment. Co-treatment with GW9662 averted telmisartan-induced rise of adiponectin. Tumor necrosis factor a declined in telmisartan-treated rats, less so with rosiglitazone, but not valsartan. Telmisartan also induced downsizing of epididymal adipocytes compared with valsartan. Leptin levels were significantly increased by valsartan (P &lt; .05) but reduced by telmisartan and rosiglitazone. The telmisartan-induced increase in adiponectin was most probably associated with a decrease in glucose and tumor necrosis factor a levels. Therefore, in addition to its hypotensive effect, telmisartan demonstrated beneficial thiazolidinedione-like effects.</description><identifier>ISSN: 0026-0495</identifier><identifier>DOI: 10.1016/j.metabol.2009.11.013</identifier><language>eng</language><subject>Adipocytes</subject><ispartof>Metabolism, clinical and experimental, 2010-08, Vol.59 (8), p.1200-1209</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Younis, Firas</creatorcontrib><creatorcontrib>Stern, Naftali</creatorcontrib><creatorcontrib>Limor, Rona</creatorcontrib><creatorcontrib>Oron, Yoram</creatorcontrib><creatorcontrib>Zangen, Sarah</creatorcontrib><creatorcontrib>Rosenthal, Talma</creatorcontrib><title>Telmisartan ameliorates hyperglycemia and metabolic profile in nonobese Cohen-Rosenthal diabetic hypertensive rats via peroxisome proliferator activator receptor-g activation</title><title>Metabolism, clinical and experimental</title><description>The importance of hypertension treatment has expanded beyond blood pressure management to include additional risk factors, mainly diabetes. It was considered of interest to test the effect of telmisartan, an angiotensin receptor 1 antagonist and peroxisome proliferator activator receptor-g partial agonist, on Cohen-Rosenthal diabetic hypertensive nonobese (CRDH) rats, a unique model combining both pathologies. Its effect was examined on fat-derived and inflammatory agents in CRDH. To determine the extent of the drug's peroxisome proliferator activator receptor-g modulating beneficial metabolic actions, results were compared with those obtained with valsartan and rosiglitazone in CRDH and Cohen diabetic rat (CDR). Telmisartan and valsartan were given in drinking water at 3 and 12 mg/kg/d, whereas rosiglitazone (3 mg/kg/d) was given as food admixture for a period of 5 months. Blood pressure, glucose, insulin, adiponectin, leptin, and tumor necrosis factor a were examined. Telmisartan and valsartan significantly (P &lt; .01) reduced blood pressure, whereas telmisartan and rosiglitazone considerably reduced blood glucose levels to normoglycemic levels (P &lt; .01) in these 2 strains. Insulin levels were not affected by telmisartan and valsartan but were slightly reduced by rosiglitazone in CDR. In contrast to valsartan, adiponectin was significantly (60%, P &lt; .01) increased by telmisartan in both CDR and CRDH, whereas rosiglitazone induced a 60% and 180% increase in CRDH and CDR animals, respectively, on day 30 of treatment. Co-treatment with GW9662 averted telmisartan-induced rise of adiponectin. Tumor necrosis factor a declined in telmisartan-treated rats, less so with rosiglitazone, but not valsartan. Telmisartan also induced downsizing of epididymal adipocytes compared with valsartan. Leptin levels were significantly increased by valsartan (P &lt; .05) but reduced by telmisartan and rosiglitazone. The telmisartan-induced increase in adiponectin was most probably associated with a decrease in glucose and tumor necrosis factor a levels. Therefore, in addition to its hypotensive effect, telmisartan demonstrated beneficial thiazolidinedione-like effects.</description><subject>Adipocytes</subject><issn>0026-0495</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2010</creationdate><recordtype>article</recordtype><recordid>eNqNz8FOwzAMBuAcQGIwHgHJN04tztq13XkCcUa7T27nrpnSpMTZxF6KZyRM487Jv-xfn2SlnjTmGnX1cshHjtR6my8QV7nWOeriRs0QF1WG5Wp5p-5FDohY1001U98btqMRCpEc0MjW-ECRBYbzxGFvzx2PhoDcDq6w6WAKvjeWwThw3vmWhWHtB3bZhxd2cSALO0Mtx1S-QJGdmBNDsgVOCUw7_2XEj_yrWdNzOvkA1EVzuqTAHU8pZPu_pfFurm57ssKP1_mgnt9eN-v3LCGfR5a4Tc90bC059kfZ1suyabDURfH_5g9Vh286</recordid><startdate>20100801</startdate><enddate>20100801</enddate><creator>Younis, Firas</creator><creator>Stern, Naftali</creator><creator>Limor, Rona</creator><creator>Oron, Yoram</creator><creator>Zangen, Sarah</creator><creator>Rosenthal, Talma</creator><scope>7U7</scope><scope>C1K</scope></search><sort><creationdate>20100801</creationdate><title>Telmisartan ameliorates hyperglycemia and metabolic profile in nonobese Cohen-Rosenthal diabetic hypertensive rats via peroxisome proliferator activator receptor-g activation</title><author>Younis, Firas ; Stern, Naftali ; Limor, Rona ; Oron, Yoram ; Zangen, Sarah ; Rosenthal, Talma</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_7548804133</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2010</creationdate><topic>Adipocytes</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Younis, Firas</creatorcontrib><creatorcontrib>Stern, Naftali</creatorcontrib><creatorcontrib>Limor, Rona</creatorcontrib><creatorcontrib>Oron, Yoram</creatorcontrib><creatorcontrib>Zangen, Sarah</creatorcontrib><creatorcontrib>Rosenthal, Talma</creatorcontrib><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><jtitle>Metabolism, clinical and experimental</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Younis, Firas</au><au>Stern, Naftali</au><au>Limor, Rona</au><au>Oron, Yoram</au><au>Zangen, Sarah</au><au>Rosenthal, Talma</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Telmisartan ameliorates hyperglycemia and metabolic profile in nonobese Cohen-Rosenthal diabetic hypertensive rats via peroxisome proliferator activator receptor-g activation</atitle><jtitle>Metabolism, clinical and experimental</jtitle><date>2010-08-01</date><risdate>2010</risdate><volume>59</volume><issue>8</issue><spage>1200</spage><epage>1209</epage><pages>1200-1209</pages><issn>0026-0495</issn><abstract>The importance of hypertension treatment has expanded beyond blood pressure management to include additional risk factors, mainly diabetes. It was considered of interest to test the effect of telmisartan, an angiotensin receptor 1 antagonist and peroxisome proliferator activator receptor-g partial agonist, on Cohen-Rosenthal diabetic hypertensive nonobese (CRDH) rats, a unique model combining both pathologies. Its effect was examined on fat-derived and inflammatory agents in CRDH. To determine the extent of the drug's peroxisome proliferator activator receptor-g modulating beneficial metabolic actions, results were compared with those obtained with valsartan and rosiglitazone in CRDH and Cohen diabetic rat (CDR). Telmisartan and valsartan were given in drinking water at 3 and 12 mg/kg/d, whereas rosiglitazone (3 mg/kg/d) was given as food admixture for a period of 5 months. Blood pressure, glucose, insulin, adiponectin, leptin, and tumor necrosis factor a were examined. Telmisartan and valsartan significantly (P &lt; .01) reduced blood pressure, whereas telmisartan and rosiglitazone considerably reduced blood glucose levels to normoglycemic levels (P &lt; .01) in these 2 strains. Insulin levels were not affected by telmisartan and valsartan but were slightly reduced by rosiglitazone in CDR. In contrast to valsartan, adiponectin was significantly (60%, P &lt; .01) increased by telmisartan in both CDR and CRDH, whereas rosiglitazone induced a 60% and 180% increase in CRDH and CDR animals, respectively, on day 30 of treatment. Co-treatment with GW9662 averted telmisartan-induced rise of adiponectin. Tumor necrosis factor a declined in telmisartan-treated rats, less so with rosiglitazone, but not valsartan. Telmisartan also induced downsizing of epididymal adipocytes compared with valsartan. Leptin levels were significantly increased by valsartan (P &lt; .05) but reduced by telmisartan and rosiglitazone. The telmisartan-induced increase in adiponectin was most probably associated with a decrease in glucose and tumor necrosis factor a levels. Therefore, in addition to its hypotensive effect, telmisartan demonstrated beneficial thiazolidinedione-like effects.</abstract><doi>10.1016/j.metabol.2009.11.013</doi></addata></record>
fulltext fulltext
identifier ISSN: 0026-0495
ispartof Metabolism, clinical and experimental, 2010-08, Vol.59 (8), p.1200-1209
issn 0026-0495
language eng
recordid cdi_proquest_miscellaneous_754880413
source Elsevier ScienceDirect Journals Complete
subjects Adipocytes
title Telmisartan ameliorates hyperglycemia and metabolic profile in nonobese Cohen-Rosenthal diabetic hypertensive rats via peroxisome proliferator activator receptor-g activation
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-27T10%3A22%3A35IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Telmisartan%20ameliorates%20hyperglycemia%20and%20metabolic%20profile%20in%20nonobese%20Cohen-Rosenthal%20diabetic%20hypertensive%20rats%20via%20peroxisome%20proliferator%20activator%20receptor-g%20activation&rft.jtitle=Metabolism,%20clinical%20and%20experimental&rft.au=Younis,%20Firas&rft.date=2010-08-01&rft.volume=59&rft.issue=8&rft.spage=1200&rft.epage=1209&rft.pages=1200-1209&rft.issn=0026-0495&rft_id=info:doi/10.1016/j.metabol.2009.11.013&rft_dat=%3Cproquest%3E754880413%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=754880413&rft_id=info:pmid/&rfr_iscdi=true