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暴露于厌食药和精神药物的培养巨噬细胞中的溶酶体改变。

Lysosomal alterations in cultured macrophages exposed to anorexigenic and psychotropic drugs.

作者信息

Drenckhahn D, Kleine L, Lüllmann-Rauch R

出版信息

Lab Invest. 1976 Aug;35(2):116-23.

PMID:957602
Abstract

Cultured rat macrophages were used for an in vitro study of drug-induced lipidosis. Cells were exposed for 24 hours to equimolar concentrations (5 X 10(-5) and 1 X 10(-4) M) of the following amphiphilic (amphipathic) cationic drugs: chlorphentermine, amitriptyline, 1-chloro-amitriptyline, iprindole, noxiptiline, chlorpromazine. In addition the less amphiphilic drug phentermine was used. Ultrastructurally, the cytologic changes essentially consisted of formation of multilamellated cytoplasmic inclusions, which possessed acid phosphatase activity. The abnormal inclusions are interpreted to result from intralysosomal accumulation of polar lipids. Under the present in vitro conditions all drugs except phentermine, had similar potencies to induce such lysosomal alterations, quite in contrast to the great quantitative differences previously observed under in vivo conditions. The present results lend further support to a concept that regards a pronounced amphiphilic (amphipathic) character to be responsible for the lipidosis-inducing action of various cationic compounds. Cultured macrophages are suggested as a useful tool to investigate this structure-activity relationship, which under in vivo conditions may be obscured by superimposed parameters such as drug metabolism.

摘要

培养的大鼠巨噬细胞用于药物诱导的脂质osis的体外研究。将细胞暴露于以下两亲性(两性)阳离子药物的等摩尔浓度(5×10(-5)和1×10(-4)M)下24小时:氯苯丁胺、阿米替林、1-氯-阿米替林、茚满二酮、诺昔替林、氯丙嗪。此外,还使用了亲水性较低的药物苯丁胺。在超微结构上,细胞学变化主要包括形成具有酸性磷酸酶活性的多层细胞质内含物。异常内含物被解释为极性脂质在溶酶体内积累的结果。在目前的体外条件下,除苯丁胺外,所有药物诱导这种溶酶体改变的效力相似,这与之前在体内条件下观察到的巨大数量差异形成了鲜明对比。目前的结果进一步支持了一种观点,即认为明显的两亲性(两性)特征是各种阳离子化合物诱导脂质osis作用的原因。培养的巨噬细胞被认为是研究这种构效关系的有用工具,在体内条件下,这种关系可能会被药物代谢等叠加参数所掩盖。

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