Suppr超能文献

新型抗炎药2-(10,11-二氢-10-氧代二苯并[b,f]硫杂卓-2-基)丙酸的药理学研究。第三次通讯:对白细胞游出和肉芽组织增生的抑制作用

Pharmacological investigations of the new antiinflammatory agent 2-(10,11-dihydro-10-oxodibenzo[b,f]thiepin-2-yl)propionic acid. 3rd communication: inhibitory effects on leucocyte emigration and proliferation of granulation.

作者信息

Tsurumi K, Mibu H, Okada K, Hasegawa J, Fujimura H

出版信息

Arzneimittelforschung. 1986 Dec;36(12):1806-9.

PMID:3566841
Abstract

The effects of 2-(10,11-dihydro-10-oxodibenzo [b,f]thiepin-2-yl)propionic acid (CN-100), which has a significant inhibitory effect on acute inflammatory reactions, on leucocyte emigration and proliferation of granulation were examined in this study. The compound obviously inhibited the protein exudation and polymorph emigration 6 h after application of carboxymethylcellulose pouch method. It also definitely inhibited the monocyte emigration occurring 24 h after carrageenin pleurisy, and the inhibitory activity of the compound was nearly equal to that of pranoprofen and weaker than that of indometacin. CN-100 inhibited the proliferation of granulation in the test by paper disk method, i.e., the compound inhibited wound healing. The antigranulation activity of CN-100 was also nearly equal to that of pranoprofen and weaker than that of indometacin. These results proved that CN-100 should definitely inhibit the reactions of the second and third inflammatory phases of the whole reactions from the exudative phase throughout proliferative phase, suggesting that the compound is a useful antiinflammatory drug.

摘要

本研究考察了对急性炎症反应有显著抑制作用的2-(10,11-二氢-10-氧代二苯并[b,f]硫杂卓-2-基)丙酸(CN-100)对白细胞游出和肉芽组织增生的影响。采用羧甲基纤维素囊袋法给药6小时后,该化合物明显抑制了蛋白质渗出和多形核白细胞游出。它也确实抑制了角叉菜胶性胸膜炎24小时后发生的单核细胞游出,该化合物的抑制活性与普拉洛芬几乎相当,比吲哚美辛弱。通过纸片法试验,CN-100抑制了肉芽组织增生,即该化合物抑制了伤口愈合。CN-100的抗肉芽组织增生活性也与普拉洛芬几乎相当,比吲哚美辛弱。这些结果证明,CN-100肯定能抑制从渗出期到增殖期整个反应过程中第二和第三炎症阶段的反应,表明该化合物是一种有用的抗炎药。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验