Ahotupa M, Hartiala K, Aitio A
Acta Pharmacol Toxicol (Copenh). 1979 May;44(5):359-63. doi: 10.1111/j.1600-0773.1979.tb02345.x.
The present study describes the effects of tetraethyl lead on various drug metabolizing enzymes in different tissues of the rat. Tetraethyl lead was administered intraperitoneally to rats (250 mumol/kg) on two consecutive days. The animals were killed on day 3. Tetraethyl lead-treatment decreased the concentration of hepatic cytochrome P-450 (to 45 per cent of the control), the hepatic activity of aryl hydrocarbon hydroxylase (to 41 per cent of the control) and ethoxycoumarin deethylase (to 45 per cent of the control). Epoxide hydratase activity was enhanced in the liver (1.3-fold), kidney (3.3-fold), and small intestinal mucosa (4.7-fold). The activity of glutathione S-transferase decreased in the liver (to 69 per cent of the control) but increased in the kidney (1.5-fold) and small intestinal mucosa (1.7-fold). The glucuronidation of o-aminophenol was enhanced (2.2-fold) in the kidney of tetraethyl lead treated rats. It is concluded that exposure to tetraethyl lead brings about widespread changes in the ability of mammals to detoxify foreign compounds.
本研究描述了四乙基铅对大鼠不同组织中各种药物代谢酶的影响。连续两天给大鼠腹腔注射四乙基铅(250微摩尔/千克)。在第3天处死动物。四乙基铅处理降低了肝细胞色素P-450的浓度(降至对照的45%)、芳烃羟化酶的肝脏活性(降至对照的41%)和乙氧基香豆素脱乙基酶的活性(降至对照的45%)。环氧化物水化酶活性在肝脏(1.3倍)、肾脏(3.3倍)和小肠黏膜(4.7倍)中增强。谷胱甘肽S-转移酶的活性在肝脏中降低(降至对照的69%),但在肾脏中增加(1.5倍),在小肠黏膜中增加(1.7倍)。在四乙基铅处理的大鼠肾脏中,邻氨基酚的葡萄糖醛酸化增强(2.2倍)。得出的结论是,接触四乙基铅会使哺乳动物对外源化合物解毒能力发生广泛变化。