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Curcumin Attenuates Oxaliplatin-Induced Liver Injury and Oxidative Stress by Activating the Nrf2 Pathway

机译:姜黄素通过激活NRF2途径衰减Oxaliplatin诱导的肝损伤和氧化应激

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Purpose: Oxaliplatin (OXA)-induced liver injury is one of the main limiting factors affecting the efficacy of OXA-based chemotherapy in patients with colorectal liver metastases. In addition, oxidative stress is an important pathophysiological mechanism of OXA-induced liver injury. Therefore, dietary antioxidants may decrease or prevent hepatic toxicity in vivo and be beneficial to OXA-based chemotherapy. Methods: An experimental OXA-induced liver injury animal model was established, and the protective effects of curcumin (CUR) against OXA-induced liver injury were investigated. ELISA was used to determine the levels of MDA, SOD, CAT, and GSH in liver tissue. The effect of CUR treatment on the expression of cytokines and the Nrf2 pathway was determined by real-time PCR and Western blotting. Results: CUR treatment alleviated OXA-induced hepatic pathological damage and splenomegaly. The protective effect of CUR was demonstrated to be correlated with inhibition of oxidative stress, inflammation, and the coagulation system. Furthermore, Western blotting revealed that CUR treatment reverses the suppression of Nrf2 nuclear translocation and increases the expression of HO-1 and NOQ1 in mice with OXA-induced liver injury. Moreover, the Nrf2 activation and hepatoprotective effect of CUR were abolished by brusatol. Conclusion: Curcumin attenuates oxaliplatin-induced liver injury and oxidative stress by activating the Nrf2 pathway, which suggests that CUR may be potentially used in the prevention and treatment of OXA-induced liver injury.
机译:目的:oxaliplatin(Oxa)诱导的肝损伤是影响氧气基化疗在结肠直肠肝转移患者中的疗效的主要限制因素之一。此外,氧化应激是Oxa诱导的肝损伤的重要病理生理机制。因此,膳食抗氧化剂可能降低或预防体内肝毒性,并有利于基于氧气的化疗。方法:建立了实验氧诱导的肝损伤动物模型,研究了姜黄素(CUR)对OXA诱导的肝损伤的保护作用。 ELISA用于确定肝组织中MDA,SOD,猫和GSH的水平。 Cur处理对细胞因子和NRF2途径表达的影响是通过实时PCR和Western印迹测定的。结果:Cur治疗缓解了Oxa诱导的肝病理损伤和脾肿大。 Cur的保护作用被证明与抑制氧化应激,炎症和凝血系统相关。此外,Western印迹显示,Cur处理逆转NRF2核转位的抑制,并增加HO-1和NOQ1在具有氧气诱导的肝损伤的小鼠中的表达。此外,Cur的NRF2活化和Cur的HepatoPotective效应被褐发醇废除。结论:通过激活NRF2途径姜黄素衰减奥沙利铂诱导的肝损伤和氧化应激,这表明Cur可能用于预防和治疗OXA诱导的肝损伤。

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