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大鼠口服苯乙烯的肝脏效应。

Hepatic effects of orally administered styrene in rats.

作者信息

Srivastava S P, Das M, Mushtaq M, Chandra S V, Seth P K

出版信息

J Appl Toxicol. 1982 Aug;2(4):219-22. doi: 10.1002/jat.2550020411.

Abstract

Adult male rats receiving styrene by gavage (200 or 400 mg kg-1, 6 days a week) for 100 days exhibited a significant dose-dependent increase in hepatic benzo[a]pyrene hydroxylase and aminopyrine-N-demethylase, a decrease in glutathione-S-transferase and no change in glucose-6-phosphatase. A decrease in the activity of mitochondrial succinic dehydrogenase and beta-glucuronidase was also observed. Activity of acid phosphatase was decreased only at the higher dose level. Levels of serum glutamic oxaloacetic transaminase and glutamic pyruvic transaminase were elevated only at the higher dose level. The absolute and relative weights of the liver of control and treated animals showed no significant difference. Histopathological studies of the liver tissue revealed tiny areas of focal necrosis, consisting of few degenerated hepatocytes and inflammatory cells at the higher dose level only.

摘要

成年雄性大鼠每周6天经口灌胃给予苯乙烯(200或400毫克/千克),持续100天,结果显示,肝脏苯并[a]芘羟化酶和氨基比林-N-脱甲基酶显著呈剂量依赖性增加,谷胱甘肽-S-转移酶减少,葡萄糖-6-磷酸酶无变化。还观察到线粒体琥珀酸脱氢酶和β-葡萄糖醛酸酶活性降低。仅在较高剂量水平下酸性磷酸酶活性降低。血清谷氨酸草酰乙酸转氨酶和谷氨酸丙酮酸转氨酶水平仅在较高剂量水平下升高。对照动物和处理动物肝脏的绝对重量和相对重量无显著差异。肝组织的组织病理学研究仅在较高剂量水平下发现微小的局灶性坏死区域,由少数变性肝细胞和炎性细胞组成。

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