Emergency Hospital, Faculty of Medicine, Mansoura University, Mansoura 35516, Egypt.
Int Immunopharmacol. 2018 Aug;61:29-36. doi: 10.1016/j.intimp.2018.05.007. Epub 2018 May 23.
Hepatotoxicity induced by cyclophosphamide (Cyclo) is a major concern in clinical practice. This study was designed to investigate the possible cytoprotective effect of natural antioxidants as oleuropein and quercetin against Cyclo induced hepatotoxicity via the nuclear factor erythroid 2-related factor 2 (Nrf2)/heme oxygenase-1 (HO-1) signaling pathway. Male Wistar rats were randomly divided into six groups and treated for 10 days as follow: Group I (Normal control) received saline, group II (Oleu control): received orally oleuropein 30 mg/kg/day, group III (Quer control): administered orally quercetin 50 mg/kg/day, group IV (Cyclo): received saline and injected with single intraperitoneal (i.p) dose of Cyclo 200 mg/kg at day 5, group V (Oleu ttt): treated with oleuropein plus Cyclo i.p. injection at day 5, and group VI (Quer ttt): treated with quercetin plus Cyclo i.p. injection at day 5. Injection of Cyclo showed marked increase in serum transaminases and alkaline phosphatase, hepatic malondialdehyde (MDA) and tumor necrosis factor-alpha (TNF-⍺) levels along with significant reduction in hepatic reduced glutathione (GSH), superoxide dismutase (SOD), and catalase levels in addition to downregulation of hepatic Nrf2 and HO-1 expressions and reduction in hepatic nuclear Nrf2 binding activity when compared with normal group. Histopathological examination of Cyclo treated rats revealed hepatic damage. Both oleuropein and quercetin exhibited an improvement in the biochemical and histopathological findings. In conclusion, the natural antioxidants oleuropein and quercetin counteract the Cyclo induced hepatotoxicity through activation of Nrf2/HO-1 signaling pathway with subsequent suppression of oxidative stress and inflammation.
环磷酰胺(Cyclo)引起的肝毒性是临床实践中的一个主要关注点。本研究旨在通过核因子红细胞 2 相关因子 2(Nrf2)/血红素加氧酶-1(HO-1)信号通路,研究天然抗氧化剂橄榄苦苷和槲皮素对 Cyclo 诱导的肝毒性的可能细胞保护作用。雄性 Wistar 大鼠随机分为六组,连续 10 天处理如下:第 I 组(正常对照组)给予生理盐水,第 II 组(橄榄苦苷对照组)给予橄榄苦苷 30mg/kg/天,第 III 组(槲皮素对照组)给予槲皮素 50mg/kg/天,第 IV 组(环磷酰胺组)给予生理盐水,并在第 5 天给予单次腹腔内(i.p.)注射环磷酰胺 200mg/kg,第 V 组(橄榄苦苷预处理组)在第 5 天给予橄榄苦苷预处理联合环磷酰胺 i.p.注射,第 VI 组(槲皮素预处理组)在第 5 天给予槲皮素预处理联合环磷酰胺 i.p.注射。与正常组相比,环磷酰胺注射显示血清转氨酶和碱性磷酸酶、肝丙二醛(MDA)和肿瘤坏死因子-α(TNF-α)水平显著增加,肝还原型谷胱甘肽(GSH)、超氧化物歧化酶(SOD)和过氧化氢酶水平显著降低,肝 Nrf2 和 HO-1 表达下调,肝核 Nrf2 结合活性降低,同时 Cyclo 处理大鼠的组织病理学检查显示肝损伤。橄榄苦苷和槲皮素均改善了生化和组织病理学发现。总之,天然抗氧化剂橄榄苦苷和槲皮素通过激活 Nrf2/HO-1 信号通路,随后抑制氧化应激和炎症,对抗 Cyclo 诱导的肝毒性。