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脓毒症中针对血小板活化因子、类花生酸和缓激肽的治疗选择。

Therapeutic options directed against platelet activating factor, eicosanoids and bradykinin in sepsis.

作者信息

Fink M P

机构信息

Department of Surgery, Beth Israel Deaconess Medical Center, Boston, MA, USA.

出版信息

J Antimicrob Chemother. 1998 Jan;41 Suppl A:81-94. doi: 10.1093/jac/41.suppl_1.81.

Abstract

Various autacoids, including the eicosanoids, platelet activating factor (PAF) and bradykinin, have been implicated in the pathogenesis of sepsis and septic shock. The precise role of these compounds as mediators of the diffuse inflammatory state characteristic of sepsis remains to be determined, but, in animal models, beneficial effects have been observed as a result of treatment with various inhibitors of eicosanoid biosynthesis or antagonists of PAF or bradykinin receptors. To date, however, it has been impossible to translate these encouraging results from animal models into convincingly positive results in the clinical setting.

摘要

包括类二十烷酸、血小板活化因子(PAF)和缓激肽在内的多种自体活性物质已被认为与脓毒症和感染性休克的发病机制有关。这些化合物作为脓毒症特征性弥漫性炎症状态介质的确切作用仍有待确定,但是,在动物模型中,使用类二十烷酸生物合成的各种抑制剂或PAF或缓激肽受体拮抗剂进行治疗已观察到有益效果。然而,迄今为止,还无法将这些来自动物模型的令人鼓舞的结果转化为临床上令人信服的阳性结果。

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