articleProceedings of the National Academy of SciencesAug 16, 2004Closed access

Nociceptor-specific gene deletion reveals a major role for Na v 1.7 (PN1) in acute and inflammatory pain

University College London

PubMed
Indexed incrossrefpubmed

Abstract

Nine voltage-gated sodium channels are expressed in complex patterns in mammalian nerve and muscle. Three channels, Na(v)1.7, Na(v)1.8, and Na(v)1.9, are expressed selectively in peripheral damage-sensing neurons. Because there are no selective blockers of these channels, we used gene ablation in mice to examine the function of Na(v)1.7 (PN1) in pain pathways. A global Na(v)1.7-null mutant was found to die shortly after birth. We therefore used the Cre-loxP system to generate nociceptor-specific knockouts. Na(v)1.8 is only expressed in peripheral, mainly nociceptive, sensory neurons. We knocked Cre recombinase into the Na(v)1.8 locus to generate heterozygous mice expressing Cre recombinase in Na(v)1.8-positive…

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683
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Authors

7

Topics & keywords

Keywords
  • Nociceptor
  • Nociception
  • Noxious stimulus
  • Gene knockout
  • Hyperalgesia
  • Sodium channel
  • Knockout mouse
  • Conditional gene knockout
UN Sustainable Development Goals
  • Good health and well-being
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