胃芬津的毒理学特征。其促性腺作用]。

Problemi na khigienata Pub Date : 1996-01-01
P Ilieva, L Ivanova-Chemishanska, G Antov
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引用次数: 0

摘要

对雄性大鼠口服胃芬津45天和90天(每天,每周5次)的促性腺作用进行了评价。实验剂量为1/20、1/100和1/200 LD50,分别为33.8、6.7和3.4 mg.kg-1。使用了功能和形态学的研究方法——精子细胞的数量、特征和移动性、抗酸性和抗渗透性、精子管内精子细胞的平均数量、精子发生指数、睾丸的形态特征以及测定顶体蛋白水解活性的放射自显影法。无论使用期限如何,最高剂量(33.8 mg.kg-1)在顶体保留蛋白水解活性时,会引起表征生精上皮功能指标的系统性偏差和形态参数的生理波动。慢性口服胃麻素3个月时,1/20 LD50 (33.8 mg.kg-1)的剂量对性腺有效,促性腺毒性活性阈值约为1/100 LD50-6.7 mg.kg-1。
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[The toxicological characteristics of Gastrofenzin. IV. Its gonadotropic action].

An evaluation of the gonadotropic effect of Gastrofenzin has been carried out in conditions of 45-day and 90-day oral application (daily, 5 times per week) in male white rats. The experiments are performed in doses 1/20, 1/100 and 1/200 LD50, respectively 33.8, 6.7 and 3.4 mg.kg-1. Functional and morphologic methods of investigation have been used-count, character and mobility, acid and osmotic resistance of the sperm cells, mean number of sperm cells in the sperm tube, spermatogenesis' indices, morphological characteristic of the testes as well as autoradiographic method for determining the proteolytic activity of the acrosome. Irrespective of the application term the highest dose (33.8 mg.kg-1) causes systemic deviations in the functional indicators and physiologic fluctuation of the morphologic parameters characterizing the spermatogenic epithelium at preserved proteolytic activity of the acrosome. The dose 1/20 LD50 (33.8 mg.kg-1) is considered to be effective on the gonads in conditions of three-month chronic oral application of Gastrofensin and the threshold of the gonadotoxic activity is about 1/100 LD50-6.7 mg.kg-1.

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