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氯喹及其他几种两亲性阳离子药物对大鼠脉络丛的不同作用。

Differential effects of chloroquine and of several other amphiphilic cationic drugs upon rat choroid plexus.

作者信息

Frisch W, Lüllmann-Rauch R

出版信息

Acta Neuropathol. 1979 May 15;46(3):203-8. doi: 10.1007/BF00690845.

Abstract

Several cationic amphiphilic drugs, each of which is known to induce generalized lipidosis in rats, were compared with respect to their cytological effects on rat choroid plexus epithelium. Chloroquine induced large cytoplasmic vacuoles, whereas the other drugs (quinacrine, 4,4'-diethylaminoethoxyhexestrol, chlorphentermine, iprindole, 1-chloro-amitriptyline, clomipramine) caused formation of lamellated or crystalloid inclusions as usually seen in drug-induced lipidosis. The ultrastructure of the chloroquine-induced vacuoles suggested storage of water-soluble materials (polar lipids and/or non-lipid materials) in addition to non-water-soluble polar lipids.

摘要

几种阳离子两亲性药物,每种药物都已知会在大鼠中诱发全身性脂质沉积,就它们对大鼠脉络丛上皮细胞的细胞学影响进行了比较。氯喹诱导形成大的细胞质空泡,而其他药物(奎纳克林、4,4'-二乙氨基乙氧基己烷雌酚、氯苯丁胺、茚满丙胺、1-氯阿米替林、氯米帕明)则导致形成层状或晶体状包涵体,这是药物诱导脂质沉积中常见的现象。氯喹诱导形成的空泡的超微结构表明,除了非水溶性极性脂质外,还储存了水溶性物质(极性脂质和/或非脂质物质)。

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