Protective Effect of Boswellic Acids against Doxorubicin-Induced Hepatotoxicity: Impact on Nrf2/HO-1 Defense Pathway

被引:73
|
作者
Barakat, Bassant M. [1 ]
Ahmed, Hebatalla I. [1 ]
Bahr, Hoda I. [2 ]
Elbahaie, Alaaeldeen M. [3 ]
机构
[1] Al Azhar Univ, Fac Pharm Girls, Dept Pharmacol & Toxicol, Cairo, Egypt
[2] Suez Canal Univ, Fac Vet Med, Dept Biochem, Ismailia, Egypt
[3] Suez Canal Univ, Fac Med, Dept Clin Oncol & Nucl Med, Ismailia, Egypt
关键词
INDUCED CARDIOTOXICITY; RATS INVOLVEMENT; CELL-DEATH; IN-VITRO; OXYGENASE-1; NRF2; INJURY; HEME; TRANSCRIPTION; METABOLISM;
D O I
10.1155/2018/8296451
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The current study aimed to investigate the potential protective role of boswellic acids (BAs) against doxorubicin-(DOX-) induced hepatotoxicity. Also, the possible mechanisms underlying this protection; antioxidant, as well as the modulatory effect on the Nrf2 transcription factor/hem oxygenase-1 (Nrf2/HO-1) pathway in liver tissues, was investigated. Animals were allocated to five groups: group 1: the saline control, group 2: the DOX group, animals received DOX (6 mg/kg, i.p.) weekly for a period of three weeks, and groups 3-5: animals received DOX (6 mg/kg, i.p.) weekly and received protective doses of BAs (125, 250, and 500 mg/kg/day). Treatment with BAs significantly improved the altered liver enzyme activities and oxidative stress markers. This was coupled with significant improvement in liver histopathological features. BAs increased the Nrf2 and HO-1 expression, which provided protection against DOX-induced oxidative insult. The present results demonstrated that BAs appear to scavenge ROS and inhibit lipid peroxidation and DNA damage of DOX-induced hepatotoxicity. The antioxidant efficacy of BAs might arise from its modulation of the Nrf2/HO-1 pathway and thereby protected liver from DOX-induced oxidative injury.
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页数:10
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