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dc.contributor.authorShahid, Muhammad Hassaan-
dc.contributor.authorAnjum, Irfan-
dc.contributor.authorMushtaq, Muhammad Naveed-
dc.contributor.authorRiaz, Saba-
dc.date.accessioned2022-10-24T08:48:30Z-
dc.date.available2022-10-24T08:48:30Z-
dc.date.issued2021-01-16-
dc.identifier.issn1011-601X-
dc.identifier.urihttp://142.54.178.187:9060/xmlui/handle/123456789/13588-
dc.description.abstractThe aim of the present study was to evaluate the cardioprotective activity of boswellic acids in doxorubicin (DOX) induced cardiotoxicity. DOX (2.5mg/kg) was used intraperitoneally in rats to induce cardiotoxicity in six divided doses every alternate day over a period of two weeks. Dexrazoxane (10:1) was used as a standard drug. Boswellic acids (250, 500 and 750 mg/kg) were orally administered to rats for 14 days. After 14 days, rats were sacrificed, and blood was withdrawn through cardiac puncture. The blood lipid profile and cardiac biomarkers including LDH, CK-MB, CPK, SGOT and troponin T were measured. The heart of rats was isolated for histopathological studies. Graphpad Prism was used for statistical analysis. There was a significant increase in the level of cardiac enzymes and complete lipid profile parameters in diseased group as compared to control group. Pre-treatment with boswellic acids decreased level of all the measured parameters and decreased the severity of myocardial damage as supported by histopathological studies. It was concluded that boswellic acids possess cardioprotective potential by lowering cardiac biomarkers and blood lipid profile. Thus, boswellic acids might act as cardioprotective agent against doxorubicin induced cardiotoxicity.en_US
dc.language.isoenen_US
dc.publisherKarachi: Faculty of Pharmacy & Pharmaceutical Sciecnes, University of Karachien_US
dc.subjectBoswellic acidsen_US
dc.subjectcardiac biomarkersen_US
dc.subjectcardioprotectiveen_US
dc.subjectdoxorubicinen_US
dc.titleCardioprotective effect of boswellic acids against doxorubicin induced myocardial infarction in ratsen_US
dc.typeArticleen_US
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