Pomegranate reverses methotrexate-induced oxidative stress and apoptosis in hepatocytes by modulating Nrf2-NF-κB pathways

被引:126
作者
Mukherjee, Sudeshna [1 ]
Ghosh, Sayan [1 ]
Choudhury, Sreetama [1 ]
Adhikary, Arghya [2 ]
Manna, Krishnendu [1 ]
Dey, Sanjit [1 ]
Sa, Gaurisankar [2 ]
Das, Tanya [2 ]
Chattopadhyay, Sreya [1 ]
机构
[1] Univ Calcutta, Dept Physiol, Kolkata 700009, W Bengal, India
[2] Bose Inst, Div Mol Med, Kolkata 700054, W Bengal, India
关键词
Pomegranate; Methotrexate; Hepatotoxicity; Oxidative stress; Nrf2; NF-kappa B; Apoptosis; NF-KAPPA-B; ANTIOXIDANT ACTIVITY; HEME OXYGENASE-1; LIVER-DAMAGE; RAT MODEL; EXTRACT; HEPATOTOXICITY; INFLAMMATION; CONSUMPTION; ACTIVATION;
D O I
10.1016/j.jnutbio.2013.07.005
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The clinical efficacy of the widely used chemotherapeutic drug methotrexate (MTX) is limited due to its associated hepatotoxicity. Pomegranate polyphenols are of huge health benefits and known to possess remarkable antioxidant properties capable of protecting normal cells from various stimuli-induced oxidative stress and cell death. In this study, we explored the protective role of pomegranate fruit extract (PFE) in ameliorating MTX-induced hepatic damage. Male Swiss albino mice exposed to MTX (20 mg/kg body weight) exhibited distinct markers of toxicity such as increased activities of enzymes alanine transaminase, aspartate transaminase, lactate dehydrogenase and alkaline phosphatase and also increased oxidative stress in liver evidenced by increased ROS generation and lipid peroxidation. Decrease in reduced glutathione levels, superoxide dismutase, catalase, hepatic heme oxygenase 1 and NQO-1 activities were also observed. Tracing the signal transduction pathways, it was seen that MTX exposure significantly increased nuclear translocation of NF-kappa B coupled with increase in phosphorylated I kappa-B and down-regulation of NF-kappaB-dependent antiapoptotic protein Bcl-2. Treatment with MIX increased the expression of the apoptotic enhancer Rho/Cdc42 as well as the phosphorylation of SAPK/JNK. A shift in the Bax/Bcl-2 ratio towards apoptosis and increase in the caspase 3 level was also evident. Administration of PFE for 7 consecutive days before and after MTX challenge suppressed MIX-induced cell death, mitigated the injurious effects of MTX and offered protection against apoptosis. PFE was shown to reduce ROS generation in hepatocytes by activating the Nrf2-ARE pathway and inhibiting NF-kappa B as a consequence of which the antioxidant defense mechanism in the liver was up-regulated, thereby conferring protection against MTX-induced hepatotoxicity and apoptosis. (C) 2013 Elsevier Inc. All rights reserved.
引用
收藏
页码:2040 / 2050
页数:11
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