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急性和慢性镉处理对雄性大鼠肝脏药物代谢的影响。

Effect of acute and chronic cadmium treatment on hepatic drug metabolism in male rats.

作者信息

Schnell R C, Yuhas E M, Pence D H, Means J R, Roberts S A, Yau E T, Miya T S, Mennear J H

出版信息

Arch Toxicol. 1978 Aug 9;40(4):269-77. doi: 10.1007/BF00310332.

DOI:10.1007/BF00310332
PMID:581260
Abstract

The effect of acute and chronic cadmium administration on hepatic drug metabolism was investigated in the male rat. 3 days after the acute administration of cadmium by either the intraperitoneal (0.84 mg Cd/kg) or the oral (greater than 80 mg Cd/kg) route, there was a significant potentiation in duration of hexobarbital hypnosis and inhibition of hepatic microsomal metabolism of hexobarbital and aniline. Administration of cadmium in the drinking water at levels of 100 or 200 ppm Cd for periods of 2--12 weeks or at levels of 5 or 20 ppm Cd for 50 weeks did not produce alterations in either drug response or hepatitic drug metabolism. Significant levels of metallothionein, a cadmium binding protein, found in the liver of the rats receiving cadmium chronically may offer an explanation for the observed differences in drug metabolism between the acute and chronic administration of cadmium. In additional studies, pretreatment of the rats with subthreshold doses of cadmium (0.21 or 0.42 mg Cd/kg) intraperitoneally produced a tolerance to the alterations in drug metabolism induced by the previous cadmium dose (0.84 mg Cd/kg, i.p.). However, chronic cadmium treatment (5 or 20 ppm Cd for 50 weeks) did not impart any such tolerance to subsequently administered Cd (0.84 mg/kg) by the intraperitoneal route. The hepatic levels of metallothionein induced by the chronic cadmium treatment were only 30--60% of those induced by the subthreshold cadmium and thus may not have bound enough of the large challenge cadmium dose to produce the tolerance phenomenon.

摘要

研究了急性和慢性给予镉对雄性大鼠肝脏药物代谢的影响。通过腹腔注射(0.84毫克镉/千克)或口服(大于80毫克镉/千克)途径急性给予镉3天后,己巴比妥催眠持续时间显著延长,己巴比妥和苯胺的肝脏微粒体代谢受到抑制。以100或200 ppm镉的水平在饮用水中给予镉2 - 12周,或以5或20 ppm镉的水平给予50周,均未引起药物反应或肝脏药物代谢的改变。在长期接受镉的大鼠肝脏中发现的大量金属硫蛋白(一种镉结合蛋白),可能为急性和慢性给予镉后观察到的药物代谢差异提供了解释。在另外的研究中,用阈下剂量的镉(0.21或0.42毫克镉/千克)腹腔内预处理大鼠,可使其对先前镉剂量(0.84毫克镉/千克,腹腔注射)诱导的药物代谢改变产生耐受性。然而,慢性镉处理(5或20 ppm镉,持续50周)并未使随后腹腔注射的镉(0.84毫克/千克)产生任何此类耐受性。慢性镉处理诱导的肝脏金属硫蛋白水平仅为阈下镉诱导水平的30% - 60%,因此可能没有结合足够多的大量挑战性镉剂量以产生耐受现象。

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Arch Toxicol. 1978 Aug 9;40(4):269-77. doi: 10.1007/BF00310332.
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本文引用的文献

1
Virtual absence of turnover in cadmium metabolism: Cd109 studies in the mouse.镉代谢中几乎不存在周转:小鼠体内的Cd109研究
Am J Physiol. 1961 Nov;201:927-30. doi: 10.1152/ajplegacy.1961.201.5.927.
2
A study of the distribution and retention of cadmium-115 in the albino rat.对白化大鼠体内镉 - 115的分布与滞留的研究。
Arch Biochem Biophys. 1957 Jan;66(1):140-5. doi: 10.1016/0003-9861(57)90544-1.
3
The fate of pentobarbital in man and dog and a method for its estimation in biological material.戊巴比妥在人和狗体内的代谢情况及其在生物材料中的测定方法。
Arch Toxicol. 1985 Jan;56(3):167-9. doi: 10.1007/BF00333421.
4
Studies on cadmium-induced inhibition of hepatic microsomal drug biotransformation in the rat.镉诱导大鼠肝微粒体药物生物转化抑制的研究。
Environ Health Perspect. 1979 Feb;28:273-9. doi: 10.1289/ehp.7928273.
J Pharmacol Exp Ther. 1953 Sep;109(1):26-34.
4
Toxic effects of cadmium: a review.镉的毒性作用:综述
Environ Res. 1971 Apr;4(2):71-85. doi: 10.1016/0013-9351(71)90036-3.
5
Cadmium inhibition of hepatic drug metabolism in the rat.镉对大鼠肝脏药物代谢的抑制作用。
Toxicol Appl Pharmacol. 1974 May;28(2):284-91. doi: 10.1016/0041-008x(74)90015-5.
6
Cadmium-induced potentiation of hexobarbital sleep time in rats.镉对大鼠戊巴比妥睡眠时间的增强作用。
Experientia. 1974 May 15;30(5):528-9. doi: 10.1007/BF01926332.
7
Stimulation of liver detoxication enzymes by dietary cadmium acetate.
Bull Environ Contam Toxicol. 1973 Dec;10(6):328-32. doi: 10.1007/BF01720998.
8
Effects of acute and subacute cadmium administration on carbohydrate metabolism in mice.
Toxicol Appl Pharmacol. 1973 Oct;26(2):231-40. doi: 10.1016/0041-008x(73)90256-1.
9
Gastrointestinal absorption of different compounds of 115m cadmium and the effect of different concentrations in the rat.115m镉不同化合物在大鼠体内的胃肠道吸收及不同浓度的影响
Environ Res. 1973 Jun;6(2):159-64. doi: 10.1016/0013-9351(73)90029-7.
10
Binding of cadmium ions by rat liver and kidney.镉离子与大鼠肝脏和肾脏的结合。
Biochem Pharmacol. 1972 Oct 15;21(20):2751-65. doi: 10.1016/0006-2952(72)90023-8.