Tag Hend M
Zoology Department, Faculty of Sciences, Suez Canal University, Ismaillia, 41522, Egypt.
BMC Complement Altern Med. 2015 Jul 25;15:252. doi: 10.1186/s12906-015-0744-y.
Drug-induced liver injury is a major health problem that challenges not only health care professionals but also the pharmaceutical industry and drug regulatory agencies. The possible hepatoprotective effect of the administration of mulberry ethanolic extract (MUL) leaves against hepatotoxic effect of the anti-rheumatic drug, methotrexate (MTX) was evaluated in this study both vivo (using animal models) and in vitro (human hepatoma HepG2 cells).
In the in-vivo study, 20 male albino rats were equally assigned into four groups; control group received distilled water orally; MUL treated-group received 500 mg/kg/day of MUL extract; MTX treated-group was injected with a single dose of 20 mg/kg MTX intraperitoneally on the 4th day; MUL-MTX treated-group received the previously mentioned doses of MUL and MTX (both control and MUL treated groups were administered a single dose of a physiological saline i.p.). At the end of the experimental period (14 days) activities of alanine transaminase (ALT), aspartate transaminase (AST), alkaline phosphatase (ALP) and lactate dehydrogenase (LDH) as well as total serum protein (TP) and albumin (ALB) levels were evaluated to assess liver function.
A marked reduction in the viability of HepG2 cells was observed after 48 h with IC50 equal to 14.5 μg/mL of MUL administration. Treating the animals with MUL in combination with MTX mitigated liver injury, causing a significant reduction in activities of AST, ALT, ALP and LDH as compared to the MTX-group. The liver architecture revealed more or less normal appearance with the combined treatment when compared with MTX treatment alone.
This study recommends that the co-administration of MUL with MTX that may have therapeutic benefits against MTX-hepato-cytotoxicity.
药物性肝损伤是一个重大的健康问题,不仅对医疗保健专业人员构成挑战,也对制药行业和药品监管机构构成挑战。本研究通过体内(使用动物模型)和体外(人肝癌HepG2细胞)实验,评估了桑椹乙醇提取物(MUL)对抗风湿药物甲氨蝶呤(MTX)肝毒性作用的潜在保肝作用。
在体内研究中,将20只雄性白化大鼠平均分为四组;对照组口服蒸馏水;MUL治疗组每天接受500mg/kg的MUL提取物;MTX治疗组在第4天腹腔注射单剂量20mg/kg的MTX;MUL-MTX治疗组接受上述剂量的MUL和MTX(对照组和MUL治疗组均腹腔注射单剂量生理盐水)。在实验期结束时(14天),评估丙氨酸转氨酶(ALT)、天冬氨酸转氨酶(AST)、碱性磷酸酶(ALP)和乳酸脱氢酶(LDH)的活性以及总血清蛋白(TP)和白蛋白(ALB)水平,以评估肝功能。
给予MUL 48小时后,观察到HepG2细胞活力显著降低,IC50等于14.5μg/mL。与MTX组相比,用MUL联合MTX治疗动物可减轻肝损伤,使AST、ALT、ALP和LDH的活性显著降低。与单独使用MTX治疗相比,联合治疗时肝脏结构显示出或多或少的正常外观。
本研究建议,MUL与MTX联合使用可能对MTX肝细胞毒性具有治疗益处。