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Bv8/PK2 和动力蛋白受体:一个可药物干预的促痛觉系统。

Bv8/PK2 and prokineticin receptors: a druggable pronociceptive system.

机构信息

Department of Physiology and Pharmacology Vittorio Erspamer, Sapienza, University of Rome, P.le A. Moro 5, 00185 Rome, Italy.

出版信息

Curr Opin Pharmacol. 2012 Feb;12(1):62-6. doi: 10.1016/j.coph.2011.10.023. Epub 2011 Nov 30.

Abstract

Mammalian Bv8 (also called prokineticin 2) is a secreted protein that regulates diverse biological processes including pain perception. It belongs to a new family of chemokines, which activate two G-protein linked receptors (prokineticin receptor 1 and 2, PKR1 and PKR2) expressed in regions of the nervous system associated with pain and in cells participating to immuno-inflammatory responses. Primary sensitive neurons co-express PKRs and the transient potential receptor vanilloid 1, cooperating in nociceptor sensitization. Bv8, strongly upregulated in neutrophils and other inflammatory cells, is a main pronociceptive mediator in inflamed tissues, where it sensitizes peripheral nociceptors, stimulates neutrophil chemotaxis and modulates the release of inflammatory and pronociceptive cytokines. Availability of a nonpeptide PKR antagonist, leading to blockade of the Bv8/PKR system, ameliorates pain arising from tissue injury and reduces the time required for recovery from injury.

摘要

哺乳动物 Bv8(也称为促动力素 2)是一种分泌蛋白,可调节包括疼痛感知在内的多种生物过程。它属于趋化因子的一个新家族,该家族可激活两种在与疼痛相关的神经系统区域和参与免疫炎症反应的细胞中表达的 G 蛋白偶联受体(促动力素受体 1 和 2,PKR1 和 PKR2)。初级敏感受体神经元共同表达 PKRs 和瞬时受体电位香草素 1,共同参与伤害感受器敏化。Bv8 在中性粒细胞和其他炎症细胞中强烈上调,是炎症组织中主要的伤害感受介质,它可使外周伤害感受器敏化,刺激中性粒细胞趋化,并调节炎症和伤害感受细胞因子的释放。非肽类 PKR 拮抗剂的出现,阻断了 Bv8/PKR 系统,可改善组织损伤引起的疼痛,并缩短损伤恢复所需的时间。

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