Iñarrea P, Gomez-Cambronero J, Pascual J, Ponte M C, Hernando L, Sánchez-Crespo M
Immunopharmacology. 1985 Feb;9(1):45-52. doi: 10.1016/0162-3109(85)90046-3.
Gram-negative sepsis was induced in rats by intraperitoneal injection of Escherichia coli. The development of bacterial peritonitis and septicemia was monitored by counting the number of peritoneal cells and by performing cultures of blood samples. Mortality reached a 50% rate when rats were injected with 2 X 10(8) colony-forming units. Rats injected with the doses of bacteria which induced mortality showed a time- and dose-dependent increase of vascular permeability as judged by the presence of abundant peritoneal exudate and by the depletion of the circulating volume. In order to know whether the generation of PAF-acether could be involved in the development of the permeability changes, the formation of this mediator was measured in the peritoneal cells and spleen of animals at different times and in response to different doses of E. coli. Significant amounts of PAF-acether could be obtained preceding the development of blood volume depletion in response to the injection of doses of E. coli which induced both mortality and the development of permeability. These data suggest that PAF-acether might be one of the inflammatory mediators involved in the pathogenesis of the hemodynamic changes observed in endotoxemia.
通过腹腔注射大肠杆菌在大鼠中诱导革兰氏阴性败血症。通过计数腹腔细胞数量和对血样进行培养来监测细菌性腹膜炎和败血症的发展。当给大鼠注射2×10⁸ 菌落形成单位时,死亡率达到50%。注射诱导死亡剂量细菌的大鼠,根据大量腹腔渗出物的存在和循环血量的减少判断,其血管通透性呈时间和剂量依赖性增加。为了了解血小板活化因子(PAF-乙醚)的生成是否可能与通透性变化的发展有关,在不同时间并针对不同剂量的大肠杆菌,测量了动物腹腔细胞和脾脏中这种介质的形成。在注射诱导死亡和通透性发展的大肠杆菌剂量后,在血容量减少之前可获得大量的PAF-乙醚。这些数据表明,PAF-乙醚可能是参与内毒素血症中观察到的血流动力学变化发病机制的炎症介质之一。