Pharmacological characterization of a rat Nav1.7 loss-of-function model with insensitivity to pain-Reference-Cited by-同舟云学术

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Pharmacological characterization of a rat Nav1.7 loss-of-function model with insensitivity to pain

Published:2020-01-17 Issue:6 Volume:161 Page:1350-1360
ISSN:0304-3959
Container-title:Pain
language:en
Short-container-title:PAIN

Author:

Chen Lubin,Effraim Philip R.,Carrara Jennifer,Zhao Peng,Dib-Hajj Fadia B.,Dib-Hajj Sulayman D.,Waxman Stephen G.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Anesthesiology and Pain Medicine,Clinical Neurology,Neurology

Reference57 articles.

1. Cannabinoids mediate analgesia largely via peripheral type 1 cannabinoid receptors in nociceptors;Agarwal;Nat Neurosci,2007

2. A stop codon mutation in SCN9A causes lack of pain sensation;Ahmad;Hum Mol Genet,2007

3. Neural processing of itch;Akiyama;Neuroscience,2013

4. Subtype-Selective small molecule inhibitors reveal a fundamental role for Nav1.7 in nociceptor electrogenesis, axonal conduction and presynaptic release;Alexandrou;PLoS One,2016

5. Role of the endogenous cannabinoid system in the formalin test of persistent pain in the rat;Beaulieu;Eur J Pharmacol,2000

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