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软骨形成:一种用于测量化合物致畸潜力的典型发育系统。

Chondrogenesis: a model developmental system for measuring teratogenic potential of compounds.

作者信息

Hassell J R, Horigan E A

出版信息

Teratog Carcinog Mutagen. 1982;2(3-4):325-31. doi: 10.1002/1520-6866(1990)2:3/4<325::aid-tcm1770020314>3.0.co;2-1.

Abstract

A simple test for determining the teratogenic potential of compounds is described using embryonic limb bud cells in culture. These mesenchyme cells multiply and differentiate into chondrocytes during a 6-day culture period. The extent of chondrogenesis is assessed by staining for the cartilage specific proteoglycan with alcian blue. The amount of stain is then measured spectrophotometrically. Compounds which interfere with growth or differentiation reduce the amount of proteoglycan and as a consequence, reduce alcian blue staining. Compounds can be added directly to the media or be activated using several different metabolizing systems. The dose of a compound needed to reduce alcian blue staining by 50% is designated the teratogenic potential (TP50) of that compound. TP50's of proven teratogens compare favorably with in vivo teratogenic doses of the teratogens.

摘要

描述了一种使用培养的胚胎肢芽细胞来确定化合物致畸潜力的简单测试方法。这些间充质细胞在6天的培养期内增殖并分化为软骨细胞。通过用阿尔辛蓝对软骨特异性蛋白聚糖进行染色来评估软骨形成的程度。然后用分光光度法测量染色量。干扰生长或分化的化合物会减少蛋白聚糖的量,从而减少阿尔辛蓝染色。化合物可以直接添加到培养基中,或者使用几种不同的代谢系统进行激活。使阿尔辛蓝染色减少50%所需的化合物剂量被指定为该化合物的致畸潜力(TP50)。已证实的致畸剂的TP50与致畸剂的体内致畸剂量相比具有优势。

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