Department of Therapeutic Chemistry, Division of Pharmaceutical and Drug Industries, National Research Center, Cairo 12622, Egypt.
World J Gastroenterol. 2012 Nov 28;18(44):6379-86. doi: 10.3748/wjg.v18.i44.6379.
The present study aims to clarify the protective effect of supplementation with some antioxidants, such as idebenone (200 mg/kg, ip), melatonin (10 mg/kg, ip) and arginine (200 mg/kg, ip) and their combination, on liver function (T. protein, albumin, alanine aminotransferase, aspartate aminotransferase and alkaline phosphatase), energetic parameters (adenosine triphosphate, adenosine diphosphate, adenosine monophosphate, inorganic phosphate, total adenylate, adenylate energy charge and potential phosphate). The effect on glycolytic and glycogenolytic enzymes (glucose, glycogen, glycogen phosphorylase, pyruvate kinase and phosphofructokinase against hypoxia) was also studied. The drugs were administered 24 and 1 h prior sodium nitrite intoxication. All biochemical parameters were estimated 1 h after sodium nitrite injection. Injection of sodium nitrite (75 mg/kg, sc) produced a significant disturbance in all biochemical parameters of liver function, energetic parameters and glycolytic and glycogenolytic enzymes. Hepatic damage was confirmed by histopathological examination of the liver as compared to controls. The marked changes in hepatic cells induced by sodium nitrite were completely abolished by pretreatment with the drug combination, suggesting potential protection against sodium nitrite-induced hypoxia. It could be concluded that a combination of both idebenone and melatonin or idebenone and arginine provides potential protection against sodium nitrite-induced hypoxia by improving biochemical parameters and preserving liver histology.
本研究旨在阐明补充一些抗氧化剂(如艾地苯醌(200mg/kg,ip)、褪黑素(10mg/kg,ip)和精氨酸(200mg/kg,ip)及其组合)对肝功能(T. 蛋白、白蛋白、丙氨酸转氨酶、天冬氨酸转氨酶和碱性磷酸酶)、能量参数(三磷酸腺苷、二磷酸腺苷、一磷酸腺苷、无机磷、总腺苷、腺苷酸能荷和潜在磷酸)的保护作用。还研究了它们对糖酵解和糖原分解酶(葡萄糖、糖原、糖原磷酸化酶、丙酮酸激酶和磷酸果糖激酶对缺氧的作用)的影响。药物在亚硝酸钠中毒前 24 小时和 1 小时给予。亚硝酸钠注射后 1 小时评估所有生化参数。亚硝酸钠(75mg/kg,sc)注射会显著干扰肝功能、能量参数以及糖酵解和糖原分解酶的所有生化参数。与对照组相比,肝组织病理学检查证实了肝损伤。与对照组相比,药物联合预处理完全消除了亚硝酸钠诱导的肝细胞的明显变化,提示对亚硝酸钠诱导的缺氧具有潜在的保护作用。可以得出结论,艾地苯醌和褪黑素或艾地苯醌和精氨酸的联合使用通过改善生化参数和保护肝组织提供了对亚硝酸钠诱导的缺氧的潜在保护。