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大鼠子宫和阴道上皮的实验性诱导脂变

Experimentally induced lipidosis in uterine and vaginal epithelium of rats.

作者信息

Geist S H, Lüllmann-Rauch R

机构信息

Department of Anatomy, University of Kiel, Germany.

出版信息

Ann Anat. 1994 Jan;176(1):3-9. doi: 10.1016/s0940-9602(11)80404-8.

Abstract

The purpose of this study was to investigate the effects of two lipidosis-inducing drugs (the anorectic drug chlorphentermine and the tricyclic antidepressant-imipramine) upon the estrous cycle of rats and upon the morphology of the vaginal and uterine epithelia. After two weeks of continuous administration of high daily drug doses, the estrous cycle became stagnant. Ultrastructurally, the vaginal and uterine epithelia contained storage lysosomes which were filled with undigested polar lipids appearing as multilamellated material. The uterine luminal epithelium was most severely affected. The estrous cycle was abolished also by treatment with the anorexigenic drug phentermine, although this compound does not cause lipidosis. Therefore, the cessation of the estrous cycle cannot be attributed to the lipidosis as induced by chlorphentermine and imipramine; probably it is a consequence of the main actions of these psychotropic drugs. The biological basis for the exceedingly severe lipidosis in the uterine luminal epithelium is suggested to be the heavy load of polar lipids physiologically delivered to the lysosomal apparatus as long as the cycle-dependent apoptotic and autophagic processes were going on during the early period of drug treatment.

摘要

本研究的目的是调查两种致脂性药物(食欲抑制剂氯苯丁胺和三环类抗抑郁药丙咪嗪)对大鼠动情周期以及阴道和子宫上皮形态的影响。在连续两周每日给予高剂量药物后,动情周期停滞。超微结构显示,阴道和子宫上皮含有充满未消化极性脂质的储存溶酶体,这些脂质呈现为多层状物质。子宫腔上皮受影响最为严重。用食欲抑制药苯丁胺治疗也会使动情周期消失,尽管该化合物不会引起脂代谢障碍。因此,动情周期的停止不能归因于氯苯丁胺和丙咪嗪所诱导的脂代谢障碍;这可能是这些精神药物主要作用的结果。子宫腔上皮中极其严重的脂代谢障碍的生物学基础被认为是,在药物治疗早期,只要依赖周期的凋亡和自噬过程持续进行,极性脂质就会大量生理性地输送到溶酶体装置。

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