Astaxanthin effect on apoptotic biomarkers in methotrexate-induced liver injury

Sarah Saad Hamdan, Yassir Mustafa Kamal, Huda Jaber Waheed
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Abstract

Methotrexate is used in the treatment of cancer, psoriasis, rheumatoid arthritis and several other disorders. It has a hepatotoxic potential side effect. Patients who have no access to alternative medications face a serious   challenge as a result. The current study aimed to assess the apoptotic potential of methotrexate on liver cells and evaluate the hepatoprotective activity of the potent antioxidant astaxanthin, by downregulation of apoptotic biomarkers caspase 9 and caspase 3. A model of methotrexate-induced liver toxicity was employed on male rats. Thirty-six rats were divided into six groups; a negative control group, methotrexate induction group given (20 mg/kg) on day 13, three groups pretreated with astaxanthin in ascending doses (50, 75 and 100 mg/kg) for 14 days before methotrexate, and a conventional therapy group pretreated with silymarin (200mg/kg). The use of methotrexate significantly increased liver tissue caspase 9 and caspase 3 compared to the negative control. On the other side, astaxanthin used in all three doses significantly normalized these biomarkers. This study revealed that since astaxanthin significantly decreased caspase 9 and caspase 3 that are involved in the apoptotic pathway, it could be used as pretreatment in patients treated with methotrexate to alleviate its hepatotoxicity.
虾青素对甲氨蝶呤诱导肝损伤中凋亡生物标志物的影响
甲氨蝶呤用于治疗癌症、牛皮癣、类风湿性关节炎和其他几种疾病。它有潜在的肝毒性副作用。因此,无法获得替代药物的患者面临着严峻的挑战。本研究旨在通过下调凋亡生物标志物caspase 9和caspase 3来评估甲氨蝶呤对肝细胞的凋亡潜力,并评估有效抗氧化剂虾青素的肝保护活性。采用甲氨蝶呤致雄性大鼠肝毒性模型。36只大鼠分为6组;阴性对照组、甲氨蝶呤诱导组于第13天给予(20 mg/kg)甲氨蝶呤治疗,三组在甲氨蝶呤治疗前分别给予虾青素(50、75、100 mg/kg)逐级增加的预处理14 d,常规治疗组给予水飞蓟素(200mg/kg)预处理。与阴性对照组相比,甲氨蝶呤的使用显著增加了肝组织caspase 9和caspase 3。另一方面,所有三种剂量的虾青素都使这些生物标志物显著正常化。本研究发现虾青素可显著降低参与凋亡通路的caspase 9和caspase 3,可作为甲氨蝶呤治疗患者的预处理,减轻甲氨蝶呤的肝毒性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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