Sun X M, Hsueh W
Department of Pathology, Children's Memorial Hospital, Northwestern University, Chicago, Illinois 60614.
J Clin Invest. 1988 May;81(5):1328-31. doi: 10.1172/JCI113459.
We have developed a rat model of ischemic bowel necrosis associated with shock by injection of platelet-activating factor (PAF) or a combination of PAF and endotoxin. Recent investigations have shown that tumor necrosis factor (TNF) also induces shock and necrosis of the gastrointestinal tract. The morphological changes of TNF-induced bowel lesions are indistinguishable from those caused by PAF. The mechanism of TNF-induced bowel necrosis is unclear. In the present study, we have shown that (a) TNF caused PAF production in bowel tissue; (b) the effects of TNF and LPS on PAF production in the intestine are additive; (c) TNF and LPS are synergistic in inducing bowel necrosis; and (d) TNF-induced bowel necrosis is due to PAF release and can be prevented by pretreatment with PAF antagonists.
我们通过注射血小板活化因子(PAF)或PAF与内毒素的组合,建立了与休克相关的缺血性肠坏死大鼠模型。最近的研究表明,肿瘤坏死因子(TNF)也可诱导休克和胃肠道坏死。TNF诱导的肠道病变的形态学变化与PAF引起的变化无法区分。TNF诱导肠坏死的机制尚不清楚。在本研究中,我们发现:(a)TNF导致肠道组织中PAF的产生;(b)TNF和LPS对肠道中PAF产生的作用是相加的;(c)TNF和LPS在诱导肠坏死方面具有协同作用;(d)TNF诱导的肠坏死是由于PAF的释放,并且可以通过用PAF拮抗剂预处理来预防。