Zaky Hanan S, Gad Amany M, Nemr Ekram, Hassan Wedad, Abd El-Raouf Ola M, Ali Aza A
Central Administration of Pharmaceutical Affairs, Cairo, Egypt.
Department of Pharmacology, National Organization for Drug Control and Research (NODCAR), Cairo, Egypt.
J Biochem Mol Toxicol. 2018 May 25:e22162. doi: 10.1002/jbt.22162.
Possible hepatoprotective effect of Curcuma longa and/or Nigella sativa against hepatotoxicity induced by coadministration of sodium valproate (SV) and paracetamol was studied. Rats were divided into 10 groups, control groups 1, 2, 3, and 4 received vehicles, C. longa (200 mg/kg, p.o.), N. sativa (250 mg/kg, p.o.), or both herbs for 21 days, respectively. Toxicity groups 5, 6, and 7 received SV (300 mg/kg, i.p.), paracetamol (1000 mg/kg, p.o.) for the last 4 days or both for 21 days, respectively. Protection groups 8, 9, and 10 received C. longa, N. sativa, or both, respectively, 1 h before the administration of both the drugs for 21 days. SV and/or paracetamol significantly increased aspartate aminotransferase (AST), alanine aminotransferase (ALT), alkaline phosphatase (ALP), total bilirubin, relative liver/body weight ratio, malondialdehyde (MDA), tumor necrosis factor alpha (TNF-α), and caspase-3 (Casp-3) while significantly decreased albumin, total protein, glutathione (GSH) reduced, GSH peroxidase, and superoxide dismutase (SOD). Preadministration of C. longa and/or N. sativa caused protective effect against the hepatotoxicity induced by both drugs.
研究了姜黄和/或黑种草籽对丙戊酸钠(SV)和对乙酰氨基酚联合给药所致肝毒性的潜在保肝作用。将大鼠分为10组,对照组1、2、3和4分别给予赋形剂、姜黄(200mg/kg,口服)、黑种草籽(250mg/kg,口服)或两种草药,持续21天。毒性组5、6和7分别在最后4天给予SV(300mg/kg,腹腔注射)、对乙酰氨基酚(1000mg/kg,口服)或两种药物联合给药21天。保护组8、9和10在两种药物给药前1小时分别给予姜黄、黑种草籽或两者,持续21天。SV和/或对乙酰氨基酚显著升高了天冬氨酸转氨酶(AST)、丙氨酸转氨酶(ALT)、碱性磷酸酶(ALP)、总胆红素、相对肝/体重比、丙二醛(MDA)、肿瘤坏死因子α(TNF-α)和半胱天冬酶-3(Casp-3),同时显著降低了白蛋白、总蛋白、还原型谷胱甘肽(GSH)、谷胱甘肽过氧化物酶和超氧化物歧化酶(SOD)。预先给予姜黄和/或黑种草籽对两种药物所致的肝毒性具有保护作用。