Chieli E, Malvaldi G, Tongiani R
Toxicology. 1979 Jun-Jul;13(2):101-14.
Administration of thiobenzamide in a single dose (25 mg/100 g body wt by stomach tube) to male rats induced centrilobular necrosis, which became evident 10 h after the poisoning. In the meantime liver weight and water content underwent changes, glycogen was lost, triglycerides accumulated in the liver while decreasing in serum, [3H] leucine uptake in proteins was impaired and the activity of glucose-6-phosphatase and aminopyrine demethylase decreased. The activity of NADPH-cytochrome c reductase remained unchanged, whereas a reduction of the microsomal cytochrome P-450 occurred. The liver amount of reduced glutathione underwent no significant changes. Pretreatment of the animals with cobalt chloride or 20-methylcholanthrene decreased the liver damage caused by the drug. The in vitro addition of thiobenzamide to liver microsomes resulted in a spectral change. The appearance of conjugated dienes among microsomal lipids from drug-treated rats indicated for a lipoperoxidation taking place in vivo.
给雄性大鼠经胃管单次注射硫代苯甲酰胺(25毫克/100克体重)会诱发小叶中心坏死,中毒后10小时变得明显。与此同时,肝脏重量和含水量发生变化,糖原流失,肝脏中甘油三酯积累而血清中甘油三酯减少,蛋白质中[3H]亮氨酸摄取受损,葡萄糖-6-磷酸酶和氨基比林脱甲基酶活性降低。NADPH-细胞色素c还原酶活性保持不变,而微粒体细胞色素P-450减少。肝脏中还原型谷胱甘肽含量无明显变化。用氯化钴或20-甲基胆蒽对动物进行预处理可减轻该药物引起的肝脏损伤。在体外将硫代苯甲酰胺添加到肝微粒体中会导致光谱变化。药物处理大鼠的微粒体脂质中出现共轭二烯表明体内发生了脂质过氧化。