Exploring the antioxidant potential of Moringa oleifera leaf extracts mitigating doxorubicin-induced cardiotoxicity in male rats
Doxorubicin (DOX) is a commonly used drug in chemotherapy for cancer treatment. However, it can cause the threatening side effect of cardiotoxicity. This study investigates whether the hydro-alcoholic leaves of have any protective potential against DOX-induced cardiotoxicity. The phytochemical analy...
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Published in: | Journal of advanced pharmaceutical technology and research Vol. 15; no. 3; pp. 166 - 170 |
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Main Authors: | , , , |
Format: | Journal Article |
Language: | English |
Published: |
India
Medknow Publications & Media Pvt. Ltd
01-07-2024
Wolters Kluwer - Medknow Wolters Kluwer Medknow Publications |
Subjects: | |
Online Access: | Get full text |
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Summary: | Doxorubicin (DOX) is a commonly used drug in chemotherapy for cancer treatment. However, it can cause the threatening side effect of cardiotoxicity. This study investigates whether the hydro-alcoholic leaves of
have any protective potential against DOX-induced cardiotoxicity. The phytochemical analysis showed that the plant extracts contained bioactive compounds with antioxidant activities. The DOX-treated group confirmed a significant increment in cardiac troponin I (cTnI) and proinflammatory cytokine interleukin-6 (IL-6) levels, which indicates damage to the cardiomyocytes and also inflammation. However, treatment with the
extracts significantly inhibited DOX-induced cardiomyocyte damage, as indicated by the significantly low cTnI release. Furthermore, treatment with
extracts further increased antioxidant activities, thereby decreasing oxidative stress and lipid peroxidation. Moreover, DOX was found to increase the IL-6 level, and treatment with
extracts had a significant impact on the inhibition of IL-6 levels. These results indicate that the
extracts have a cardioprotective effect and can play a role as an adjunct drug in mitigating DOX-induced cardiotoxicity, thus providing new prospects for the improvement of safety and efficacy in the treatment of cancer. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 2231-4040 0976-2094 |
DOI: | 10.4103/JAPTR.JAPTR_531_23 |