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氯丙嗪对大鼠不同器官转运酶活性的体内抑制作用是可逆的。

The in vivo inhibition of transport enzyme activities in different organs of rat by chlorpromazine is reversible.

作者信息

Adhikary G, Nandy P, Chandra S, Sikdar R, Sen P C

机构信息

Department of Chemistry, Bose Institute, Calcutta, India.

出版信息

Biochem Int. 1991 Dec;25(5):951-61.

PMID:1666511
Abstract

Chlorpromazine, an antipsychotic drug is found to inhibit Na+K(+)-ATPase, Ca(2+)-ATPase and acetylcholinesterase activities in the microsomal membranes of rat in vivo, when the drug is injected for certain periods of time. The inhibition seems to be due to the changes in fatty acid composition of lipid and microviscosity of the membranes. However, once the drug has been withdrawn, the enzyme activities are found to return to the normal level in three to five weeks, suggesting that the drug effect is reversible.

摘要

抗精神病药物氯丙嗪在大鼠体内注射一定时间后,被发现会抑制大鼠微粒体膜中的钠钾 - ATP酶、钙 - ATP酶和乙酰胆碱酯酶的活性。这种抑制作用似乎是由于膜脂质脂肪酸组成和微粘度的变化所致。然而,一旦停药,酶活性在三到五周内会恢复到正常水平,这表明药物作用是可逆的。

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The in vivo inhibition of transport enzyme activities in different organs of rat by chlorpromazine is reversible.氯丙嗪对大鼠不同器官转运酶活性的体内抑制作用是可逆的。
Biochem Int. 1991 Dec;25(5):951-61.
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The chlorpromazine inhibition of transport ATPase and acetylcholinesterase activities in the microsomal membranes of rat in vitro and in vivo.
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The effect of binding of chlorpromazine and chloroquine to ion transporting ATPases.氯丙嗪和氯喹与离子转运ATP酶结合的作用。
Mol Cell Biochem. 1999 Aug;198(1-2):179-85. doi: 10.1023/a:1006902031255.