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HCN2 离子通道:作为疼痛起搏器的新兴作用。

HCN2 ion channels: an emerging role as the pacemakers of pain.

机构信息

Department of Pharmacology, University of Cambridge, Tennis Court Road, Cambridge CB2 1PD, UK.

出版信息

Trends Pharmacol Sci. 2012 Aug;33(8):456-63. doi: 10.1016/j.tips.2012.04.004. Epub 2012 May 19.

Abstract

Acute nociceptive pain is caused by the direct action of a noxious stimulus on pain-sensitive nerve endings, whereas inflammatory pain (both acute and chronic) arises from the actions of a wide range of inflammatory mediators released following tissue injury. Neuropathic pain, which is triggered by nerve damage, is often considered to be very different in its origins, and is particularly difficult to treat effectively. Here we review recent evidence showing that members of the hyperpolarization-activated cyclic nucleotide-modulated (HCN) ion channel family - better known for their role in the pacemaker potential of the heart - play important roles in both inflammatory and neuropathic pain. Deletion of the HCN2 isoform from nociceptive neurons abolishes heat-evoked inflammatory pain and all aspects of neuropathic pain, but acute pain sensation is unaffected. This work shows that inflammatory and neuropathic pain have much in common, and suggests that selective blockers of HCN2 may have value as analgesics in the treatment of pain.

摘要

急性伤害性疼痛是由有害刺激物直接作用于痛觉敏感的神经末梢引起的,而炎症性疼痛(包括急性和慢性)则是由组织损伤后释放的多种炎症介质引起的。神经病理性疼痛是由神经损伤引起的,通常被认为在起源上有很大的不同,而且特别难以有效治疗。在这里,我们回顾了最近的证据,表明超极化激活环核苷酸调节(HCN)离子通道家族的成员——在心脏起搏电位中更为人所知——在炎症性和神经性疼痛中都发挥着重要作用。删除伤害性神经元中的 HCN2 同工型可消除热诱导的炎症性疼痛和所有神经性疼痛,但急性疼痛感觉不受影响。这项工作表明,炎症性和神经性疼痛有很多共同之处,并表明 HCN2 的选择性阻滞剂可能作为治疗疼痛的镇痛药具有价值。

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