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与三环类精神药物治疗的大鼠肺和肝中类脂质性改变相关的肺泡内泡沫细胞。

Intraalveolar foam cells associated with lipidosis-like alterations in lung and liver of rats treated with tricyclic psychotropic drugs.

作者信息

Lüllmann-Rauch R, Scheid D

出版信息

Virchows Arch B Cell Pathol. 1975 Nov 21;19(3):255-68. doi: 10.1007/BF02889372.

Abstract

Histological, histochemical, and ultrastructural examinations were performed on pulmonary and hepatic tissues of rats after prolonged oral treatment with several tricyclic antidepressants and two neuroleptics, which are all of amphiphilic character. The antidepressants ipindole, imipramine, clomipramine, 1-chloro-amitriptyline, and 1-chloro-10,11-dehydro-amitriptyline were found to cause an accumulation of intraalveolar foam cells accompanied by the formation of abnormal lamellated and crystalloid cytoplasmic inclusions in most pulmonary and hepatic cell types. The ultrastructural and histochemical findings in both tissues point to generalized, abnormal intracellular storage of polar lipids, i.e. to drug-induced lipidosis. The foam cells are not regarded as an isolated pulmonary alteration but rather as an easily obtainable indication of generalized lipidosis, under the present conditions. They are thought to represent alveolar macrophages stuffed with non-digestible phospholipids. On the other hand, the tricyclic antidepressants noxiptiline and amitriptyline, and the neuroleptics chlorpromazine and thioridazine caused neither formation of foam cells nor of any lipidosis-like ultrastructural alterations. These negative results are tentatively ascribed to a more rapid biotransformation of the amphiphilic drug molecules into more hydrophilic metabolites which no longer have a high affinity to polar lipids. Two main conclusions can be drawn from the present ovservations: (1) Intraalveolar foam cells must not be regarded as a fortuitous alteration but rather as a first indication of generalized phospholipidosis, when they are found in animals treated with an amphiphilic drug. (2) Closely related compounds of amphiphilic character do not necessarily have the same potency to induce a phospholipidosis under in vivo conditions.

摘要

对大鼠经多种具有两亲性的三环类抗抑郁药和两种抗精神病药长期口服治疗后的肺组织和肝组织进行了组织学、组织化学和超微结构检查。发现抗抑郁药伊潘哚、丙咪嗪、氯米帕明、1-氯阿米替林和1-氯-10,11-脱氢阿米替林会导致肺泡内泡沫细胞积聚,并在大多数肺细胞和肝细胞类型中形成异常的层状和晶体状细胞质内含物。两种组织的超微结构和组织化学结果均表明极性脂质在细胞内普遍存在异常储存,即药物诱导的脂质osis。在目前情况下,泡沫细胞不被视为一种孤立的肺部改变,而是全身性脂质osis的一个易于获得的指标。它们被认为代表充满不可消化磷脂的肺泡巨噬细胞。另一方面,三环类抗抑郁药诺昔替林和阿米替林,以及抗精神病药氯丙嗪和硫利达嗪既不会导致泡沫细胞形成,也不会导致任何类似脂质osis的超微结构改变。这些阴性结果暂时归因于两亲性药物分子更快地生物转化为亲水性更强的代谢产物,这些代谢产物对极性脂质不再具有高亲和力。从目前的观察中可以得出两个主要结论:(1)当在接受两亲性药物治疗的动物中发现肺泡内泡沫细胞时,不应将其视为偶然改变,而应将其视为全身性磷脂osis的第一个指标。(2)具有两亲性的密切相关化合物在体内条件下不一定具有相同的诱导磷脂osis的能力。

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