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青春期前用依托泊苷处理的白化大鼠中支持细胞的功能。

Sertoli cell function in albino rats treated with etoposide during prepubertal phase.

作者信息

Stumpp Taiza, Freymüller Edna, Miraglia Sandra Maria

机构信息

Federal University of São Paulo, 740, Botucatu, São Paulo, SP, Brazil.

出版信息

Histochem Cell Biol. 2006 Sep;126(3):353-61. doi: 10.1007/s00418-006-0168-3. Epub 2006 Mar 21.

Abstract

Sertoli cell plays a key role in spermatogenesis. Many studies refer that this cell is not harmed by the majority of anticancer treatments known to cause damage to the testis. However, in the previous study we observed that etoposide, an efficient chemotherapeutic drug, provokes an increase in numerical density of the Sertoli cells. This phenomenon suggests that this cell was harmed by etoposide. Thus, we decided to investigate a possible direct action of etoposide on Sertoli cells analyzing the function of this cell and relating it with the integrity and damage of the seminiferous epithelium. Prepubertal albino rats received 5 mg/kg of etoposide for eight consecutive days and were sacrificed in different ages. The control groups received 0.9% saline solution. The testes were fixed in Bouin's liquid for transferrin immunolabeling and testicular labeled tissue volume density measurement. Except for the younger rats, all the etoposide-treated rats showed diminution of transferrin immunolabeling in the seminiferous epithelium, and consequently, of total labeled testicular tissue volume density. We concluded that the diminution of transferrin labeling in the seminiferous epithelium was not associated with germ cell absence such as commonly reported. The results suggest etoposide impairs Sertoli cell function.

摘要

支持细胞在精子发生过程中起关键作用。许多研究表明,这种细胞不会受到大多数已知会对睾丸造成损害的抗癌治疗的影响。然而,在之前的研究中,我们观察到依托泊苷(一种有效的化疗药物)会导致支持细胞的数量密度增加。这一现象表明这种细胞受到了依托泊苷的损害。因此,我们决定通过分析支持细胞的功能并将其与生精上皮的完整性和损伤联系起来,研究依托泊苷对支持细胞可能的直接作用。青春期前的白化病大鼠连续八天接受5mg/kg的依托泊苷,并在不同年龄处死。对照组接受0.9%的盐溶液。将睾丸固定在Bouin氏液中进行转铁蛋白免疫标记和睾丸标记组织体积密度测量。除了较年幼的大鼠外,所有接受依托泊苷治疗的大鼠生精上皮中的转铁蛋白免疫标记均减少,因此,总标记睾丸组织体积密度也降低。我们得出结论,生精上皮中转铁蛋白标记的减少与通常报道的生殖细胞缺失无关。结果表明依托泊苷会损害支持细胞的功能。

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