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苯巴比妥处理的大鼠暴露于二硫化碳后肝脏胆固醇代谢

Hepatic cholesterol metabolism following exposure to carbon disulfide in phenobarbital-treated rats.

作者信息

Simmons J E, Sloane R A, Van Stee E W

出版信息

Arch Environ Contam Toxicol. 1989 Sep;18(5):678-87. doi: 10.1007/BF01225006.

Abstract

Male F344 rats were exposed either to 1.87 mg/L (600 ppm) carbon disulfide (CS2) for 6 hr/day by inhalation for 1, 2, or 3 consecutive days, or to 0.1% phenobarbital (PB) in the drinking water starting 5 days before exposure to CS2, or to both. Combined treatments (CS2 + PB) resulted in a decrease in hepatic cholesterol synthesis, increases in hepatic cholesterol concentration and relative liver weight, and histopathologic damage. Maximal inhibition of cholesterol synthesis was observed following 1 day of combined treatments, while the increases in hepatic cholesterol concentration were similar following 1, 2, or 3 days of combined treatments. Exposure to CS2 only produced a pattern of inhibition of cholesterol synthesis that was similar to, though less extensive than, that seen following combined treatments. All reported alterations caused by combined treatments of CS2 + PB were reversible; recovery was, in all cases, essentially complete by day 11 after a single exposure to 1.87 mg/L CS2. With the exception of cholesterol concentration where time to recovery was decreased by continuation of PB, the time required for recovery from the effects of combined treatments of CS2 + PB was not affected by whether or not PB was continued after CS2 exposure. The reported observations support the theory that metabolism of CS2 is involved in the expression of CS2-mediated alterations of hepatic cholesterol metabolism.

摘要

雄性F344大鼠连续1天、2天或3天每天吸入1.87毫克/升(600 ppm)二硫化碳(CS2),持续6小时;或者在接触CS2前5天开始饮用含0.1%苯巴比妥(PB)的水;或者两者同时进行。联合处理(CS2 + PB)导致肝胆固醇合成减少、肝胆固醇浓度和相对肝重增加以及组织病理学损伤。联合处理1天后观察到胆固醇合成受到最大抑制,而联合处理1天、2天或3天后肝胆固醇浓度的增加相似。仅接触CS2产生的胆固醇合成抑制模式与联合处理后相似,但程度较轻。所有报道的由CS2 + PB联合处理引起的改变都是可逆的;在单次接触1.87毫克/升CS2后,所有情况下在第11天基本完全恢复。除了胆固醇浓度,继续使用PB可缩短恢复时间外,CS2接触后是否继续使用PB并不影响从CS2 + PB联合处理的影响中恢复所需的时间。所报道的观察结果支持这样一种理论,即CS2的代谢参与了CS2介导的肝胆固醇代谢改变的表达。

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