4.6 Review Book Chapter

Sodium Channels in Normal and Pathological Pain

期刊

ANNUAL REVIEW OF NEUROSCIENCE, VOL 33
卷 33, 期 -, 页码 325-347

出版社

ANNUAL REVIEWS
DOI: 10.1146/annurev-neuro-060909-153234

关键词

erythromelalgia; paroxysmal extreme pain disorder; congenital insensitivity to pain; sensory neurons; sympathetic neurons

资金

  1. NINDS NIH HHS [NS053422, R01 NS053422] Funding Source: Medline
  2. NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE [R56NS053422, R01NS053422] Funding Source: NIH RePORTER

向作者/读者索取更多资源

Nociception is essential for survival whereas pathological pain is maladaptive and often unresponsive to pharmacotherapy. Voltage-gated sodium channels, Na-v 1.1-Na-v 1.9, are essential for generation and conduction of electrical impulses in excitable cells. Human and animal studies have identified several channels as pivotal for signal transmission along the pain axis, including Na-v 1.3, Na-v 1.7, Na-v 1.8, and Na-v 1.9, With the latter three preferentially expressed in peripheral sensory neurons and Na-v 1.3 being upregulated along pain-signaling pathways after nervous system injuries. Na-v 1.7 is of special interest because it has been linked to a spectrum of inherited human pain disorders. Here we review the contribution of these sodium channel isoforms to pain.

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