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血小板活化因子作用后大鼠肠道中白三烯和去甲肾上腺素的顺序释放。血小板活化因子诱导肠道坏死的机制研究。

Sequential release of leukotrienes and norepinephrine in rat bowel after platelet-activating factor. A mechanistic study of platelet-activating factor-induced bowel necrosis.

作者信息

Hsueh W, Gonzalez-Crussi F, Arroyave J L

机构信息

Department of Pathology, Children's Memorial Hospital, Northwestern University Medical School, Chicago, Illinois.

出版信息

Gastroenterology. 1988 Jun;94(6):1412-8. doi: 10.1016/0016-5085(88)90680-4.

Abstract

We have developed a model of ischemic bowel necrosis in the rat by injecting synthetic platelet-activating factor into the mesenteric vascular bed. Our previous studies have shown that the development of ischemic necrosis was not due to thrombus formation, but to release of vasoconstricting mediators from the intestinal tissue, such as leukotriene C4. However the release of leukotriene C4 was transient and could not account for the prolonged intestinal vasoconstriction. In the present study, we show that (a) the release of norepinephrine from intestinal tissue was increased after injection of platelet-activating factor, and was responsible, at least in part, for the prolonged vasoconstriction; (b) in vivo treatment with reserpine abolished both the prolonged vasoconstriction and the release of norepinephrine from the perfused small intestine; (c) the release of norepinephrine was largely secondary to leukotriene C4 production and direct injection of leukotriene C4 caused catecholamine release; and (d) there was a concomitant release of epinephrine (of a lesser magnitude) after injection of platelet-activating factor.

摘要

我们通过向大鼠肠系膜血管床注射合成血小板活化因子,建立了大鼠缺血性肠坏死模型。我们之前的研究表明,缺血性坏死的发生并非由于血栓形成,而是由于肠道组织释放血管收缩介质,如白三烯C4。然而,白三烯C4的释放是短暂的,无法解释肠道血管的 prolonged 收缩。在本研究中,我们发现:(a) 注射血小板活化因子后,肠道组织中去甲肾上腺素的释放增加,这至少部分导致了血管收缩的 prolonged;(b) 利血平体内治疗消除了血管收缩的 prolonged 以及灌注小肠中去甲肾上腺素的释放;(c) 去甲肾上腺素的释放很大程度上继发于白三烯C4的产生,直接注射白三烯C4会导致儿茶酚胺释放;(d) 注射血小板活化因子后,同时会释放肾上腺素(量较少)。

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