4.5 Review

Voltage-gated Na+ channels in neuropathic pain

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EXPERT OPINION ON INVESTIGATIONAL DRUGS
卷 16, 期 5, 页码 635-646

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TAYLOR & FRANCIS LTD
DOI: 10.1517/13543784.16.5.635

关键词

analgesic agents; anticonvulsant agents; cancer pain; diabetic neuropathy; inflammatory pain; neuropathic pain; postherpetic neuralgia; tetrodotoxin-resistant Na+ channels; tetrodotoxin-sensitive Na+ channels; trigeminal neuralgia; voltage-gated Na+ channels

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Neuropathic pain occurs as a result of some form of injury to the nervous system. Although the basis of the disease remains to be fully elucidated, numerous studies have suggested a major role for ion channels in the pathogenesis of neuropathic pain. As Na+ channels play a fundamental role in not only the generation but also in the conduction of an action potential, they have received considerable attention in the aetiology of pain sensation and have become important pharmacological targets. In this review, the authors discuss the importance of specific Na+ channel isciforms in the pathophysiology of neuropathic pain and the present use of Na+ channel antagonists in the treatment of neuropathic pain.

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