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对乙酰氨基酚的肝毒性和微粒体功能。

Paracetamol hepatotoxicity and microsomal function.

机构信息

Department of Biochemistry, Faculty of Science, M.S. University of Baroda, Vadodara, Gujarat 390002, India.

出版信息

Environ Toxicol Pharmacol. 1999 Mar;7(1):67-74. doi: 10.1016/s1382-6689(98)00053-2.

Abstract

The effect of paracetamol-induced hepatotoxicity in rats (650 mg/kg) on microsomal function was examined. Paracetamol treatment resulted in lowered Na(+),K(+)-ATPase activity in the microsomes with decrease in V(max) of the low affinity high V(max) component II. However, the temperature kinetics was not influenced significantly. The total phospholipid and cholesterol contents as well as lipid peroxidation in the microsomes were unchanged. However, content of acidic phospholipids: phosphatidylserine and phosphatidylinositol decreased by 50% with a reciprocal increase in the sphingomyelin content; the lysophosphoglyceride content increased by 12-fold. The microsomal membrane appeared to be more fluidized following paracetamol treatment. Paracetamol treatment also resulted in a significant reduction in the sulfhydryl groups content.

摘要

研究了对乙酰氨基酚(650mg/kg)诱导的大鼠肝毒性对微粒体功能的影响。对乙酰氨基酚处理导致微粒体中 Na(+),K(+)-ATP 酶活性降低,低亲和力高 V(max) 成分 II 的 V(max)降低。然而,温度动力学没有受到显著影响。微粒体中的总磷脂和胆固醇含量以及脂质过氧化没有改变。然而,酸性磷脂:磷脂酰丝氨酸和磷脂酰肌醇的含量下降了 50%,鞘磷脂的含量相应增加;溶血甘油磷脂的含量增加了 12 倍。微粒体膜在对乙酰氨基酚处理后似乎变得更加流动。对乙酰氨基酚处理还导致巯基含量显著减少。

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