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Tumour necrosis factor and endotoxin synergistically activate intestinal phospholipase A2 in mice. Role of endogenous platelet activating factor and effect of exogenous platelet activating factor.

机译:肿瘤坏死因子和内毒素协同激活小鼠肠道磷脂酶A2。内源性血小板活化因子的作用和外源性血小板活化因子的作用。

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摘要

Previous studies have shown that: (a) platelet activating factor induces shock and intestinal injury, (b) exogenous platelet activating factor stimulates synthesis of endogenous platelet activating factor, and (c) tumour necrosis factor alpha and endotoxin synergise to induce shock and bowel injury in animals. These last two effects are largely mediated by platelet activating factor forming phospholipase A2 A2, a key enzyme for platelet activating factor synthesis, was examined in mouse intestine. It was found that tumour necrosis factor alpha and endotoxin synergise to stimulate platelet activating factor forming phospholipase A2 activity in the intestine, as well as platelet activating factor production, and these effects were blocked by pretreatment with platelet activating factor antagonists, SRI-63-441 and WEB 2086. In addition, exogenous platelet activating factor stimulates intestinal phospholipase A2 activity. These results show that tumour necrosis factor alpha and lipopolysaccharide synergistically activate the phospholipase A2 that participates in platelet activating factor formation, and this activation is largely mediated by endogenous platelet activating factor. Furthermore, platelet activating factor itself increases phospholipase A2 activity, suggesting that platelet activating factor induces its own synthesis, probably by phospholipase A2 activation.
机译:先前的研究表明:(a)血小板活化因子诱导休克和肠道损伤;(b)外源性血小板活化因子刺激内源性血小板活化因子的合成;(c)肿瘤坏死因子α和内毒素协同诱导休克和肠损伤在动物中。在小鼠肠道中检查了这最后两种作用,主要是由血小板活化因子形成磷脂酶A2 A2介导的,磷脂酶A2是血小板活化因子合成的关键酶。发现肿瘤坏死因子α和内毒素协同刺激肠道中形成血小板活化因子的磷脂酶A2活性以及血小板活化因子的产生,而这些作用被血小板活化因子拮抗剂SRI-63-441预处理所阻断和WEB2086。此外,外源性血小板活化因子刺激肠磷脂酶A2活性。这些结果表明,肿瘤坏死因子α和脂多糖协同活化参与血小板活化因子形成的磷脂酶A2,并且该活化很大程度上由内源性血小板活化因子介导。此外,血小板活化因子本身会增加磷脂酶A2的活性,提示血小板活化因子可能通过磷脂酶A2活化来诱导自身的合成。

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