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青春期前阶段用依托泊苷治疗的白化大鼠的细胞凋亡和睾丸改变。

Apoptosis and testicular alterations in albino rats treated with etoposide during the prepubertal phase.

作者信息

Stumpp Taiza, Sasso-Cerri Estela, Freymüller Edna, Miraglia Sandra Maria

机构信息

Laboratory of Embryology, Department of Morphology, Federal University of São Paulo, São Paulo, Brazil.

出版信息

Anat Rec A Discov Mol Cell Evol Biol. 2004 Jul;279(1):611-22. doi: 10.1002/ar.a.20045.

Abstract

Etoposide is a podophyllotoxin semiderivative that is used in a variety of chemotherapy treatments, including therapy for children tumors. This drug promotes the formation of a ternary DNA-topoisomerase II-etoposide complex that triggers apoptosis. The purpose of this work was to analyze the occurrence of apoptosis in the seminiferous epithelium of prepubertal, pubertal, and adult rats treated with 10, 20, and 40 mg/Kg of etoposide during the prepubertal phase, as well as the role of apoptosis in etoposide-induced testicular damage. The rat testes were fixed in Bouin's liquid, and the apoptotic cells were quantified by means of the hematoxylin and eosin (H&E) technique (all groups) and the terminal dUTP nick end labeling (TUNEL) method (prepubertal groups only). The results obtained from both the H&E and TUNEL methods showed an increased frequency of apoptosis in the seminiferous epithelium of treated animals, except for the subgroup that received the 10-mg/Kg dose and was sacrificed 12 hr after the treatment and for the etoposide-treated pubertal group, that did not show cells suggesting apoptosis during H&E analysis. The labeled cells were mainly primary spermatocytes and differentiated spermatogonia. The prepubertal rats showed an etoposide-dose-dependent diminution of differentiated spermatogonia. Etoposide treatment during the prepubertal phase increases the frequency of apoptosis in the seminiferous epithelium, and causes serious harm to male fertility. 2004.

摘要

依托泊苷是一种鬼臼毒素半衍生物,用于多种化疗治疗,包括儿童肿瘤治疗。这种药物促进三元DNA - 拓扑异构酶II - 依托泊苷复合物的形成,从而引发细胞凋亡。本研究的目的是分析青春期前、青春期和成年大鼠在青春期前阶段接受10、20和40 mg/Kg依托泊苷治疗后,生精上皮细胞凋亡的发生情况,以及凋亡在依托泊苷诱导的睾丸损伤中的作用。将大鼠睾丸固定于Bouin氏液中,通过苏木精和伊红(H&E)技术(所有组)和末端脱氧核苷酸转移酶介导的缺口末端标记(TUNEL)法(仅青春期前组)对凋亡细胞进行定量分析。H&E和TUNEL方法获得的结果均显示,治疗动物的生精上皮细胞凋亡频率增加,但接受10 mg/Kg剂量并在治疗后12小时处死的亚组以及依托泊苷治疗的青春期组除外,在H&E分析中未显示有细胞凋亡迹象。标记的细胞主要是初级精母细胞和分化的精原细胞。青春期前大鼠显示出分化精原细胞数量的依托泊苷剂量依赖性减少。青春期前阶段的依托泊苷治疗增加了生精上皮细胞的凋亡频率,并对雄性生育能力造成严重损害。2004年。

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