Zuckerman J E, Hollinger M A, Giri S N
J Pharmacol Exp Ther. 1980 Jun;213(3):425-31.
Endotracheal administration of bleomycin to hamsters causes severe pulmonary fibrosis. We have examined the utility of this response as a model for the screening of pulmonary antifibrotic agents. The time course of collagen synthesis after bleomycin administration was examined in neutral salt soluble and insoluble fractions by in vitro incubation of minced lung with [14C] proline. Collagen synthesis increased to approximately 250% above control in both neutral salt soluble and insoluble collagen fractions by day 6 after bleomycin. Noncollagenous protein synthesis was also increased but to a lesser amount. The early rise in collagen synthesis leads to accumulation of collagen that can be biochemically quantitated within 1 week. This time course is advantageous for short-term testing of antifibrotic agents. In the present study, beta-aminopropionitrile, D-penicillamine, and p-aminobenzoic acid were examined. All three agents were found to reduce significantly the accumulation of neutral salt insoluble collagen in bleomycin-treated animals.
对仓鼠进行博来霉素气管内给药会导致严重的肺纤维化。我们已经研究了这种反应作为筛选肺部抗纤维化药物模型的实用性。通过用[14C]脯氨酸对切碎的肺组织进行体外孵育,检测博来霉素给药后中性盐可溶性和不溶性部分中胶原蛋白合成的时间进程。博来霉素给药后第6天,中性盐可溶性和不溶性胶原蛋白部分的胶原蛋白合成均增加至对照水平以上约250%。非胶原蛋白合成也增加了,但增加量较少。胶原蛋白合成的早期增加导致胶原蛋白积累,可在1周内进行生化定量。这个时间进程有利于抗纤维化药物的短期测试。在本研究中,检测了β-氨基丙腈、D-青霉胺和对氨基苯甲酸。发现所有三种药物均能显著减少博来霉素治疗动物中性盐不溶性胶原蛋白的积累。