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血小板活化因子受体拮抗剂治疗急性胰腺炎

Therapy for acute pancreatitis with platelet-activating factor receptor antagonists.

作者信息

Chen Chong, Xia Shi-Hai, Chen Hong, Li Xiao-Hong

机构信息

Department of Gastroenterology, Pancreas Center of Affiliated Hospital of Medical College of Chinese People's Armed Police Forces, Tianjin 300162, China.

出版信息

World J Gastroenterol. 2008 Aug 14;14(30):4735-8. doi: 10.3748/wjg.14.4735.

Abstract

Acute pancreatitis (AP) causes release of platelet-activating factor (PAF), which induces systemic effects that contribute to circulatory disturbances and multiple organ failure. PAF is a cell surface secretion of bioactive lipid, which could produce physiological and pathological effects by binding to its cell surface receptor called platelet-activating factor receptor (PAF-R). Studies showed that PAF participate in the occurrence and development of AP and administration of platelet-activating factor receptor antagonists (PAF-RAs) could significantly reduce local and systemic events after AP. PAF has also been implicated as a key mediator in the progression of severe AP, which can lead to complications and unacceptably high mortality rates. Several classes of compounds show significant PAF-RAs, and significant local and systemic effects on reducing inflammatory changes. As a preventive treatment, PAF-RA could block a series of PAF-mediated inflammatory injury and thus improve the prognosis of AP. This review introduces the important role of PAF-RA in the treatment of AP.

摘要

急性胰腺炎(AP)会导致血小板活化因子(PAF)的释放,PAF会引发全身效应,进而导致循环系统紊乱和多器官功能衰竭。PAF是一种生物活性脂质的细胞表面分泌物,它可以通过与其细胞表面受体血小板活化因子受体(PAF-R)结合产生生理和病理效应。研究表明,PAF参与了AP的发生和发展,给予血小板活化因子受体拮抗剂(PAF-RAs)可以显著减少AP后的局部和全身事件。PAF也被认为是重症AP进展中的关键介质,重症AP可导致并发症和高得令人难以接受的死亡率。几类化合物显示出显著的PAF-RAs活性,并对减轻炎症变化有显著的局部和全身作用。作为一种预防性治疗,PAF-RA可以阻断一系列PAF介导的炎症损伤,从而改善AP的预后。这篇综述介绍了PAF-RA在AP治疗中的重要作用。

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