The cannabinoid receptor agonist CP-55,940 and ethyl arachidonate interfere with [3H]batrachotoxinin A 20 α-benzoate binding to sodium channels and inhibit sodium channel function-Reference-Cited by-同舟云学术

The cannabinoid receptor agonist CP-55,940 and ethyl arachidonate interfere with [3H]batrachotoxinin A 20 α-benzoate binding to sodium channels and inhibit sodium channel function

Published:2008-09 Issue:3 Volume:148 Page:244-249
ISSN:1532-0456
Container-title:Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology
language:en
Short-container-title:Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology

Author:

Duan Yin,Liao Chengyong,Jain Saurabh,Nicholson Russell A.

Publisher

Elsevier BV

Subject

Health, Toxicology and Mutagenesis,Cell Biology,Toxicology,Physiology,Biochemistry,General Medicine

Reference36 articles.

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2. Binding of [3H]batrachotoxinin A-20-benzoate to a receptor site associated with sodium channels in synaptic nerve ending particles;Catterall;J. Biol. Chem.,1981

3. Direct inhibition of T-type calcium channels by the endogenous cannabinoid anandamide;Chemin;EMBO J.,2001

4. Inhibition by anandamide and synthetic cannabimimetics of the release of [3H]D-aspartate and [3H]GABA from synaptosomes isolated from the rat hippocampus;D'Amico;Neurochem. Res.,2004

5. Cannabinoids modulate potassium current in cultured hippocampal neurons;Deadwyler;Recept. Channels,1993

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