Inhibition of Anandamide Hydrolysis by Cyclohexyl Carbamic Acid 3′-Carbamoyl-3-yl Ester (URB597) Reverses Abuse-Related Behavioral and Neurochemical Effects of Nicotine in Rats-Reference-Cited by-同舟云学术

Inhibition of Anandamide Hydrolysis by Cyclohexyl Carbamic Acid 3′-Carbamoyl-3-yl Ester (URB597) Reverses Abuse-Related Behavioral and Neurochemical Effects of Nicotine in Rats

Published:2008-08-25 Issue:2 Volume:327 Page:482-490
ISSN:0022-3565
Container-title:Journal of Pharmacology and Experimental Therapeutics
language:en
Short-container-title:J Pharmacol Exp Ther

Author:

Scherma Maria,Panlilio Leigh V.,Fadda Paola,Fattore Liana,Gamaleddin Islam,Le Foll Bernard,Justinová Zuzana,Mikics Eva,Haller Jozsef,Medalie Julie,Stroik Jessica,Barnes Chanel,Yasar Sevil,Tanda Gianluigi,Piomelli Daniele,Fratta Walter,Goldberg Steven R.

Publisher

American Society for Pharmacology & Experimental Therapeutics (ASPET)

Subject

Pharmacology,Molecular Medicine

Reference45 articles.

1. Activation of TRPV1 by the Satiety Factor Oleoylethanolamide

2. Pharmacological Characterization of Hydrolysis-Resistant Analogs of Oleoylethanolamide with Potent Anorexiant Properties

3. Antidepressant-like Activity of the Fatty Acid Amide Hydrolase Inhibitor URB597 in a Rat Model of Chronic Mild Stress

4. Endogenous cannabinoid anandamide inhibits nicotinic acetylcholine receptor function in mouse thalamic synaptosomes

5. Lack of CB1 cannabinoid receptors modifies nicotine behavioural responses, but not nicotine abstinence

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