King S J, Miller H R
Immunology. 1984 Apr;51(4):653-60.
The systemic secretion of rat mucosal mast cell protease (RMCPII) was examined in Nippostrongylus-primed rats injected intravenously with N. brasiliensis whole worm antigen. The secretory response in primed rats was both time- and dose-dependent whereas no RMCPII was present in the sera of naive rats challenged with antigen. RMCPII was detected in the sol and gel phases of intestinal perfusates, the release of enzyme into the gut lumen occurring very rapidly after challenge in immune rats. Mucosal permeability, assessed by measuring the passage of Evan's blue from the blood into the gut lumen was both time- and dose-dependent and reflected the combined capillary and epithelial permeability. Although the release of RMCPII into the gut lumen occurred more rapidly than the intraluminal accumulation of Evan's blue, these two events were highly correlated. There were, in addition significant correlations between the systemic and enteric secretion of RMCPII and the enteric accumulation of Evan's blue. These results indicate that RMCPII may have a role in altering intestinal mucosal permeability during systemic anaphylaxis in the rat.
在经巴西日圆线虫预致敏的大鼠静脉注射巴西日圆线虫全虫抗原后,检测大鼠黏膜肥大细胞蛋白酶(RMCPII)的全身分泌情况。预致敏大鼠的分泌反应呈时间和剂量依赖性,而用抗原攻击的未致敏大鼠血清中未检测到RMCPII。在肠道灌流液的液相和凝胶相中检测到RMCPII,免疫大鼠在攻击后酶迅速释放到肠腔中。通过测量伊文思蓝从血液进入肠腔的情况评估的黏膜通透性呈时间和剂量依赖性,反映了毛细血管和上皮的综合通透性。尽管RMCPII释放到肠腔中的速度比伊文思蓝在肠腔内的积累速度快,但这两个事件高度相关。此外,RMCPII的全身和肠道分泌与伊文思蓝在肠道内的积累之间也存在显著相关性。这些结果表明,RMCPII可能在大鼠全身过敏反应期间改变肠道黏膜通透性方面发挥作用。