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铊对睾丸细胞原代培养物的影响。

Effects of thallium on primary cultures of testicular cells.

作者信息

Gregotti C, Di Nucci A, Costa L G, Manzo L, Scelsi R, Bertè F, Faustman E M

机构信息

Institute of Pharmacology, University of Pavia, Italy.

出版信息

J Toxicol Environ Health. 1992 May;36(1):59-69. doi: 10.1080/15287399209531623.

Abstract

The objective of this in vitro study was to examine the response of mixed cultures of Sertoli and germ cells to treatment with thallium (Tl) at the range of concentrations that, in previous studies, was shown in vivo to affect reproduction. Cultures were prepared from the testis of Sprague-Dawley rats. Cultures containing approximately 3.75 x 10(6) cells/ml were treated with Tl concentrations corresponding to 35, 7, and 1.4 micrograms Tl/g testis, estimated from protein content of cultures. Observations at 24, 48, and 72 h after treatment showed a significant release of germ cells into the culture medium that was both concentration and time dependent. Cultures treated with 35 micrograms Tl/g testis showed a threefold increase in germ-cell detachment compared with controls after only 24 h of exposure. As the treatment time increased to 48 h of exposure, even cultures exposed at the lowest Tl concentration (1.4 micrograms Tl/g testis) showed significant loss of germ cells. After 48 h, cultures exposed to 7 micrograms Tl/g testis exhibited a 2.5-fold increase in germ-cell detachment, and those exposed to 35 micrograms Tl/g testis exhibited a 10-fold increase over controls. Morphological investigations of cell cultures showed evident loss of germ cells with significant reduction in prepachytene and pachytene spermatocytes and changes in the shape of Sertoli cells. These results are in agreement with in vivo studies, in which thallium treatment at comparable exposure levels manifested its earliest toxic testicular effects in Sertoli and germ cells. They also demonstrate the usefulness of this in vitro culture technique to assess toxic testicular damage rapidly.

摘要

这项体外研究的目的是检测支持细胞和生殖细胞混合培养物对铊(Tl)处理的反应,铊的浓度范围在之前的体内研究中已表明会影响生殖。培养物取自Sprague-Dawley大鼠的睾丸。含有约3.75×10⁶个细胞/毫升的培养物用铊浓度进行处理,该浓度根据培养物的蛋白质含量估算,分别对应35、7和1.4微克铊/克睾丸。处理后24、48和72小时的观察结果显示,生殖细胞向培养基中的显著释放呈浓度和时间依赖性。用35微克铊/克睾丸处理的培养物在仅暴露24小时后,生殖细胞脱离数量相比对照组增加了两倍。随着处理时间增加到48小时,即使是暴露于最低铊浓度(1.4微克铊/克睾丸)的培养物也显示出生殖细胞的显著损失。48小时后,暴露于7微克铊/克睾丸的培养物生殖细胞脱离数量增加了2.5倍,而暴露于35微克铊/克睾丸的培养物相比对照组增加了10倍。细胞培养物的形态学研究显示生殖细胞明显损失,粗线期前和粗线期精母细胞显著减少,支持细胞形状改变。这些结果与体内研究一致,在体内研究中,在相当暴露水平下的铊处理最早在支持细胞和生殖细胞中表现出其对睾丸的毒性作用。它们还证明了这种体外培养技术在快速评估睾丸毒性损伤方面的有用性。

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