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The voltage-gated sodium channel NaV 1.9 in visceral pain.
Hockley, J R F; Winchester, W J; Bulmer, D C.
Afiliação
  • Hockley JR; Wingate Institute of Neurogastroenterology, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Winchester WJ; National Centre for Bowel Research and Surgical Innovation, Blizard Institute, Barts and the London School of Medicine and Dentistry, Queen Mary University of London, London, UK.
  • Bulmer DC; Neusentis (Pfizer Ltd.), Cambridge, UK.
Neurogastroenterol Motil ; 28(3): 316-26, 2016 Mar.
Article em En | MEDLINE | ID: mdl-26462871
ABSTRACT

BACKGROUND:

Visceral pain is a common symptom for patients with gastrointestinal (GI) disease. It is unpleasant, debilitating, and represents a large unmet medical need for effective clinical treatments. Recent studies have identified NaV 1.9 as an important regulator of afferent sensitivity in visceral pain pathways to mechanical and inflammatory stimuli, suggesting that NaV 1.9 could represent an important therapeutic target for the treatment of visceral pain. This potential has been highlighted by the identification of patients who have an insensitivity to pain or painful neuropathies associated with mutations in SCN11A, the gene encoding voltage-gated sodium channel subtype 1.9 (NaV 1.9).

PURPOSE:

Here, we address the role of NaV 1.9 in visceral pain and what known human NaV 1.9 mutants can tell us about NaV 1.9 function in gut physiology and pathophysiology.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dor Visceral / Canal de Sódio Disparado por Voltagem NAV1.9 Limite: Animals / Humans Idioma: En Revista: Neurogastroenterol Motil Ano de publicação: 2016 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Dor Visceral / Canal de Sódio Disparado por Voltagem NAV1.9 Limite: Animals / Humans Idioma: En Revista: Neurogastroenterol Motil Ano de publicação: 2016 Tipo de documento: Article