Tsurufuji S, Kumakura S
Department of Biochemistry, Faculty of Pharmaceutical Science, Tohoku University, Sendai, Japan.
Dermatologica. 1989;179 Suppl 1:64-7. doi: 10.1159/000248452.
This study was done with the aid of experimental models of inflammation provoked in air pouch, which was made subcutaneously on the back of rats, by applying a carrageenin solution or a suspension of kaolin in a carboxymethylcellulose solution as an irritant. Bradykinin in the inflammatory sites, determined by an enzyme immunoassay method, were comparatively high in the earliest stage of inflammation in both the models and responsible for the exudative reactions. With the passage of time, i.e. within 20 min in the case of kaolin and 120 min in carrageenin, tissue kininase entered the inflammatory site and reduced bradykinin to a very low level, though bradykinin was still being generated very actively. In this later stage, bradykinin collaborates with prostaglandin to bring about a significant increase in the vascular permeability.
本研究借助于在大鼠背部皮下制作的气袋炎症实验模型进行,通过应用角叉菜胶溶液或高岭土在羧甲基纤维素溶液中的悬浮液作为刺激物引发炎症。采用酶免疫测定法测定炎症部位的缓激肽,在两种模型的炎症最早阶段,缓激肽水平相对较高,且是渗出反应的原因。随着时间推移,即在高岭土模型中20分钟内以及角叉菜胶模型中120分钟内,组织激肽酶进入炎症部位并将缓激肽降低至非常低的水平,尽管缓激肽仍在非常活跃地生成。在这个后期阶段,缓激肽与前列腺素协同作用,使血管通透性显著增加。