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通过药理学试剂抑制对SH基团的组织化学反应作为致畸活性的初步试验。

Inhibition of histochemical reaction to SH groups by pharmacological agents as a preliminary test for the teratogenic activity.

作者信息

Szydłowska H, Dł uzniewski A, Buczyńska B

出版信息

Pol J Pharmacol Pharm. 1980 Jul-Aug;32(4):557-65.

PMID:7255271
Abstract

Studies carried out with 34 chemicals (drugs or food additives) previously screened for the teratogenic activity revealed that the compounds which had shown teratogenic properties blocked or markedly depressed the intensity of an in vitro histochemical reaction for SH groups in fixed liver sections in Wistar rats. Most of the drugs devoid of the teratogenic activity did not affect the reaction of SH groups; only three of the compounds which did not show unequivocal teratogenic properties (but, nevertheless, produced few congenital malformations) inhibited the reaction. The results suggest that the ability of teratogenic chemicals to inhibit the histochemical reaction to SH groups in vitro may be employed in a preliminary in vitro test to screen drugs for teratogenicity.

摘要

对先前筛选过致畸活性的34种化学物质(药物或食品添加剂)进行的研究表明,显示出致畸特性的化合物会阻断或显著降低Wistar大鼠固定肝脏切片中SH基团的体外组织化学反应强度。大多数没有致畸活性的药物不会影响SH基团的反应;只有三种未表现出明确致畸特性(但仍导致少量先天性畸形)的化合物抑制了该反应。结果表明,致畸化学物质在体外抑制SH基团组织化学反应的能力可用于初步体外试验,以筛选药物的致畸性。

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