| dc.contributor.author | Sandamali, J.A.N. | |
| dc.contributor.author | Hewawasam, R.P. | |
| dc.contributor.author | Jayatilaka, K.A.P.W. | |
| dc.contributor.author | Mudduwa, L.K.B. | |
| dc.date.accessioned | 2023-01-11T09:17:18Z | |
| dc.date.available | 2023-01-11T09:17:18Z | |
| dc.date.issued | 2020-03-16 | |
| dc.identifier.citation | Sandamali, J.A.N., Hewawasam, R.P., Jayatilaka, K.A.P.W., Mudduwa, L.K.B., 2020. Cardioprotective potential of Murraya koenigii (L.) Spreng. leaf extract against doxorubicin-induced cardiotoxicity in rats. Evidence-Based Complementary and Alternative Medicine. doi: 10.1155/2020/6023737. | en_US |
| dc.identifier.issn | 1741-427X | |
| dc.identifier.issn | 1741-4288 | |
| dc.identifier.uri | http://ir.lib.ruh.ac.lk/xmlui/handle/iruor/10150 | |
| dc.description.abstract | Dose-dependent cardiotoxicity of doxorubicin may lead to irreversible congestive heart failure. Although multiple mechanisms are involved, generation of free radicals is the most commonly postulated mechanism. +erefore, free radical scavengers are considered as potential therapeutic agents. As Murraya koenigii leaves are a rich source of flavonoids and phenols, they have the ability to scavenge free radicals effectively. +erefore, the objective of this study was to investigate the cardioprotective potential of Murraya leaf extract against doxorubicin-induced cardiotoxicity in rats. Rats were randomly divided into five groups with 10 animals in each group. Doxorubicin was administered intraperitonially at 18 mg/kg while lyophilized plant extract was ad ministered orally at 2 g/kg. Dexrazoxane, at 180 mg/kg, was used as the positive control. Cardiac damage of doxorubicin control was evident with a significant increase (p < 0.05) in cardiac troponin I, NT-pro BNP, AST, and LDH compared to the normal control. Plant-treated group showed cardioprotective effect by significantly reducing (p < 0.05) all of the above parameters compared to doxorubicin control (p < 0.05). Increased oxidative stress in doxorubicin control was evident with a significant reduction in reduced glutathione, glutathione reductase, glutathione peroxidase, total antioxidant capacity, superoxide dismutase, and catalase activity and a significant increase in lipid peroxidation compared to the control. Interestingly, treatment with Murraya leaf extract showed a significant increase in all of the above antioxidant parameters and a significant reduction in lipid peroxidation by showing an antioxidant effect. A significant increase in myeloperoxidase activity confirmed the increased in flammatory activity in doxorubicin control group whereas plant-treated group showed a significant reduction (p < 0.05) which expressed the anti-inflammatory effect of Murraya leaf extract. Doxorubicin-treated group showed histological evidence of extensive damage to the myocardium while plant-treated group showed a preserved myocardium with lesser degree of damage. Pretreatment with Murraya leaf extract may replenish cardiomyocytes with antioxidants and promote the defense against doxorubicin-induced cardiotoxicity. | en_US |
| dc.language.iso | en | en_US |
| dc.publisher | Hindawi | en_US |
| dc.subject | Doxorubicin | en_US |
| dc.subject | cardiotoxicity | en_US |
| dc.subject | Murraya koenigii leaf extract | en_US |
| dc.subject | cardioprotectivity | en_US |
| dc.subject | antioxidant effect | en_US |
| dc.title | Cardioprotective potential of Murraya koenigii (L.) Spreng. leaf extract against doxorubicin-induced cardiotoxicity in rats | en_US |
| dc.type | Article | en_US |