Journal
EUROPEAN JOURNAL OF PHARMACOLOGY
Volume 720, Issue 1-3, Pages 310-319Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.ejphar.2013.10.011
Keywords
Nicotinic receptors; Cannabidiol; Cannabinoids; Xenopus oocyte
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Funding
- CMHS, UAE University
- LABCO partner of Sigma-Aldrich
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The effects of cannabidiol (CBD), a non-psychoactive ingredient of cannabis plant, on the function of the cloned alpha(7) subunit of the human nicotinic acetylcholine (alpha(7) nACh) receptor expressed in Xenopus oocytes were tested using the two-electrode voltage-clamp technique. CBD reversibly inhibited ACh (100 mu M)-induced currents with an IC50 value of 11.3 mu M. Other phytocannabinoids such as cannabinol and Delta(9)-tetrahydrocannabinol did not affect ACh-induced currents. CBD inhibition was not altered by pertussis toxin treatment. In addition, CBD did not change GTP-gamma-5 binding to the membranes of oocytes injected with alpha(7) nACh receptor cRNA. The effect of CBD was not dependent on the membrane potential. CBD (10 mu M) did not affect the activity of endogenous Ca2+-dependent Cl- channels, since the extent of inhibition by CBD was unaltered by intracellular injection of the Ca2+ chelator BAPTA and perfusion with Ca2+-free bathing solution containing 2 mM Ba2+. Inhibition by CBD was not reversed by increasing ACh concentrations. Furthermore, specific binding of [I-125] alpha-bungarotoxin was not inhibited by CBD (10 mu M) in oocytes membranes. Using whole cell patch clamp technique in CA1 stratum radiatum interneurons of rat hippocampal slices, currents induced by choline, a selective-agonist of alpha(7)-receptor induced currents were also recoded. Bath application of CBD (10 mu M) for 10 min caused a significant inhibition of choline induced currents. Finally, in hippocampal slices, [H-3] norepinephrine release evoked by nicotine (30 mu M) was also inhibited by 10 mu M CBD. Our results indicate that CBD inhibits the function of the alpha(7)-nACh receptor. (C) 2013 Elsevier B.V. All rights reserved.
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