Hsueh W, González-Crussi F, Arroyave J L
Department of Pathology, Children's Memorial Hospital, Northwestern University, Chicago, Illinois 60614.
FASEB J. 1987 Nov;1(5):403-5. doi: 10.1096/fasebj.1.5.3678700.
We have developed a model of isochemic bowel necrosis in the rat by injecting platelet-activating factor (PAF) or PAF in combination with bacterial endotoxin. PAF causes profound hypotension, and it has been suggested that it is released during endotoxin shock. Because ischemic bowel necrosis is often associated with shock or infection, it is possible that PAF is the endogenous mediator that causes shock and bowel necrosis during sepsis. In this study, we have demonstrated that: 1) normal intestine contained a small amount of PAF; 2) necrotic lesions of the intestine could be induced by endotoxin injection; 3) PAF production in the bowel is markedly increased in animals treated with endotoxin; 4) pretreatment of the animal with PAF antagonists prevent endotoxin-induced necrosis; 5) isolated, buffer-perfused small intestine produced a small quantity of PAF in response to endotoxin injection. Therefore, we conclude that PAF is a likely endogenous mediator in endotoxemia, which causes bowel necrosis and shock.
我们通过注射血小板活化因子(PAF)或PAF与细菌内毒素的组合,建立了大鼠缺血性肠坏死模型。PAF可导致严重低血压,并且有人提出它在内毒素休克期间释放。由于缺血性肠坏死常与休克或感染相关,因此PAF有可能是脓毒症期间导致休克和肠坏死的内源性介质。在本研究中,我们证明了:1)正常肠道含有少量PAF;2)注射内毒素可诱导肠道坏死病变;3)在内毒素处理的动物中,肠道中PAF的产生显著增加;4)用PAF拮抗剂预处理动物可预防内毒素诱导的坏死;5)分离的、用缓冲液灌注的小肠在注射内毒素后产生少量PAF。因此,我们得出结论,PAF可能是内毒素血症中的内源性介质,它可导致肠坏死和休克。