{"title":"Investigating the Possible Cardio-Protective Effects of Telmisartan against 5-Fluorouracil- Induced Cadiotoxicity in Wister Rats","authors":"A. Khudhair, I. T. Numan","doi":"10.9734/bpi/tipr/v7/9749d","DOIUrl":null,"url":null,"abstract":"Objective: The present study was designed to investigate the protective effects of telmisartan against 5-FU induced cardiotoxicity in Wister rats.\nMethods: Thirty-six Wister rats were randomly divided into six groups: I, negative control receiving normal saline (2 ml/kg) orally for 30 successive days; II, positive control receiving normal saline (2ml/kg/day) orally for 25 days, and subsequently received 5-Fluorouracil (5-FU) (20 mg in 2 ml normal saline per kg body weight) once daily by intraperitoneal injection in association with normal saline for a 5 days; III and IV, receiving telmisartan (5mg and 10mg/kg/day) respectively for 30 successive days; V and VI, receiving telmisartan (5 mg and 10 mg/kg/day) orally for 25 days, and subsequently received 5-FU (20 mg in 2ml normal saline per kg body weight) once daily by intraperitoneal injection in association with normal saline for a 5 days respectively.\nResults: Prophylactic treatment of telmisartan significantly attenuates the serum cardiac troponin T, aspartate Aminotransferase (AST) and alanine.\nAminotransferase (ALT) elevation caused by 5-FU-induced cardiotoxicity.\nConclusion: results of the present finding suggest that telmisartan may be a useful modulator in mitigating 5-FU induced cardiotoxicity.","PeriodicalId":355376,"journal":{"name":"Technological Innovation in Pharmaceutical Research Vol. 7","volume":"10 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2021-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Technological Innovation in Pharmaceutical Research Vol. 7","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.9734/bpi/tipr/v7/9749d","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
Objective: The present study was designed to investigate the protective effects of telmisartan against 5-FU induced cardiotoxicity in Wister rats.
Methods: Thirty-six Wister rats were randomly divided into six groups: I, negative control receiving normal saline (2 ml/kg) orally for 30 successive days; II, positive control receiving normal saline (2ml/kg/day) orally for 25 days, and subsequently received 5-Fluorouracil (5-FU) (20 mg in 2 ml normal saline per kg body weight) once daily by intraperitoneal injection in association with normal saline for a 5 days; III and IV, receiving telmisartan (5mg and 10mg/kg/day) respectively for 30 successive days; V and VI, receiving telmisartan (5 mg and 10 mg/kg/day) orally for 25 days, and subsequently received 5-FU (20 mg in 2ml normal saline per kg body weight) once daily by intraperitoneal injection in association with normal saline for a 5 days respectively.
Results: Prophylactic treatment of telmisartan significantly attenuates the serum cardiac troponin T, aspartate Aminotransferase (AST) and alanine.
Aminotransferase (ALT) elevation caused by 5-FU-induced cardiotoxicity.
Conclusion: results of the present finding suggest that telmisartan may be a useful modulator in mitigating 5-FU induced cardiotoxicity.