Rutin and Quercetin Counter Doxorubicin-Induced Liver Toxicity in Wistar Rats via Their Modulatory Effects on Inflammation, Oxidative Stress, Apoptosis, and Nrf2

被引:53
作者
Ahmed, Osama M. [1 ]
Elkomy, Mohammed H. [2 ]
Fahim, Hanaa I. [1 ]
Ashour, Mohamed B. [1 ]
Naguib, Ibrahim A. [3 ]
Alghamdi, Badrah S. [4 ,5 ]
Mahmoud, Heba Uallah R. [1 ]
Ahmed, Noha A. [1 ]
机构
[1] Beni Suef Univ, Div Physiol, Dept Zool, Fac Sci, POB 62521, Bani Suwayf, Egypt
[2] Jouf Univ, Dept Pharmaceut, Coll Pharm, Sakaka 72341, Saudi Arabia
[3] Taif Univ, Dept Pharmaceut Chem, Coll Pharm, POB 11099, Taif 21944, Saudi Arabia
[4] King Abdulaziz Univ, Dept Physiol, Neurosci Unit, Fac Med, Jeddah 22252, Saudi Arabia
[5] King Abdulaziz Univ, Preclin Res Unit, King Fahd Med Res Ctr, Jeddah, Saudi Arabia
关键词
INDUCED HEPATOTOXICITY; INDUCED CARDIOTOXICITY; ADRIAMYCIN; FLAVONOIDS; CANCER; NANOPARTICLES; MITOCHONDRIA; SUPPRESSION; METABOLISM; INHIBITORS;
D O I
10.1155/2022/2710607
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The presented study was performed to verify whether rutin and/or quercetin can inhibit liver injury induced by doxorubicin (DXR) in male Wistar rats. In this study, male Wistar rats were treated via the oral route with rutin and quercetin (50 mg/kg) either alone or in combination every other day for five weeks concomitant with receiving intraperitoneal DXR (2 mg/kg) two times a week for five successive weeks. Quercetin, rutin, and their combination significantly improved the deteriorated serum AST, ALT, and ALP activities and total bilirubin level, as well as albumin, AFP, and CA 19.9 levels in DXR-injected rats. Treatments of the DXR-injected group with quercetin and rutin prevented the elevation in liver lipid peroxidation and the reduction in superoxide dismutase, glutathione-S-transferase and glutathione peroxidase activities, and glutathione content. Treatments with quercetin and rutin significantly repressed the elevated expression of liver p53 and TNF-alpha and enhanced Nrf2 expression. Furthermore, the treatments significantly reduced DXR-induced liver histological changes. In conclusion, rutin and quercetin either alone or in combination may have potential preventive effects against DXR-induced hepatotoxicity through inhibiting oxidative stress, inflammation, and apoptosis as well as modulating the Nrf2 expression.
引用
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页数:19
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