Endocannabinoid regulation of acute and protracted nicotine withdrawal: effect of FAAH inhibition.

Evidence shows that the endocannabinoid system modulates the addictive properties of nicotine. In the present study, we hypothesized that spontaneous withdrawal resulting from removal of chronically implanted transdermal nicotine patches is regulated by the endocannabinoid system. A 7-day nicotine d...

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Main Authors: Andrea Cippitelli, Giuseppe Astarita, Andrea Duranti, Giovanni Caprioli, Massimo Ubaldi, Serena Stopponi, Marsida Kallupi, Gianni Sagratini, Fernando Rodrìguez de Fonseca, Daniele Piomelli, Roberto Ciccocioppo
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3227620?pdf=render
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spelling doaj-9919a6d6605546feb5537f933b7256e12020-11-24T22:00:07ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-01611e2814210.1371/journal.pone.0028142Endocannabinoid regulation of acute and protracted nicotine withdrawal: effect of FAAH inhibition.Andrea CippitelliGiuseppe AstaritaAndrea DurantiGiovanni CaprioliMassimo UbaldiSerena StopponiMarsida KallupiGianni SagratiniFernando Rodrìguez de FonsecaDaniele PiomelliRoberto CiccocioppoEvidence shows that the endocannabinoid system modulates the addictive properties of nicotine. In the present study, we hypothesized that spontaneous withdrawal resulting from removal of chronically implanted transdermal nicotine patches is regulated by the endocannabinoid system. A 7-day nicotine dependence procedure (5.2 mg/rat/day) elicited occurrence of reliable nicotine abstinence symptoms in Wistar rats. Somatic and affective withdrawal signs were observed at 16 and 34 hours following removal of nicotine patches, respectively. Further behavioral manifestations including decrease in locomotor activity and increased weight gain also occurred during withdrawal. Expression of spontaneous nicotine withdrawal was accompanied by fluctuation in levels of the endocannabinoid anandamide (AEA) in several brain structures including the amygdala, the hippocampus, the hypothalamus and the prefrontal cortex. Conversely, levels of 2-arachidonoyl-sn-glycerol were not significantly altered. Pharmacological inhibition of fatty acid amide hydrolase (FAAH), the enzyme responsible for the intracellular degradation of AEA, by URB597 (0.1 and 0.3 mg/kg, i.p.), reduced withdrawal-induced anxiety as assessed by the elevated plus maze test and the shock-probe defensive burying paradigm, but did not prevent the occurrence of somatic signs. Together, the results indicate that pharmacological strategies aimed at enhancing endocannabinoid signaling may offer therapeutic advantages to treat the negative affective state produced by nicotine withdrawal, which is critical for the maintenance of tobacco use.http://europepmc.org/articles/PMC3227620?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Andrea Cippitelli
Giuseppe Astarita
Andrea Duranti
Giovanni Caprioli
Massimo Ubaldi
Serena Stopponi
Marsida Kallupi
Gianni Sagratini
Fernando Rodrìguez de Fonseca
Daniele Piomelli
Roberto Ciccocioppo
spellingShingle Andrea Cippitelli
Giuseppe Astarita
Andrea Duranti
Giovanni Caprioli
Massimo Ubaldi
Serena Stopponi
Marsida Kallupi
Gianni Sagratini
Fernando Rodrìguez de Fonseca
Daniele Piomelli
Roberto Ciccocioppo
Endocannabinoid regulation of acute and protracted nicotine withdrawal: effect of FAAH inhibition.
PLoS ONE
author_facet Andrea Cippitelli
Giuseppe Astarita
Andrea Duranti
Giovanni Caprioli
Massimo Ubaldi
Serena Stopponi
Marsida Kallupi
Gianni Sagratini
Fernando Rodrìguez de Fonseca
Daniele Piomelli
Roberto Ciccocioppo
author_sort Andrea Cippitelli
title Endocannabinoid regulation of acute and protracted nicotine withdrawal: effect of FAAH inhibition.
title_short Endocannabinoid regulation of acute and protracted nicotine withdrawal: effect of FAAH inhibition.
title_full Endocannabinoid regulation of acute and protracted nicotine withdrawal: effect of FAAH inhibition.
title_fullStr Endocannabinoid regulation of acute and protracted nicotine withdrawal: effect of FAAH inhibition.
title_full_unstemmed Endocannabinoid regulation of acute and protracted nicotine withdrawal: effect of FAAH inhibition.
title_sort endocannabinoid regulation of acute and protracted nicotine withdrawal: effect of faah inhibition.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description Evidence shows that the endocannabinoid system modulates the addictive properties of nicotine. In the present study, we hypothesized that spontaneous withdrawal resulting from removal of chronically implanted transdermal nicotine patches is regulated by the endocannabinoid system. A 7-day nicotine dependence procedure (5.2 mg/rat/day) elicited occurrence of reliable nicotine abstinence symptoms in Wistar rats. Somatic and affective withdrawal signs were observed at 16 and 34 hours following removal of nicotine patches, respectively. Further behavioral manifestations including decrease in locomotor activity and increased weight gain also occurred during withdrawal. Expression of spontaneous nicotine withdrawal was accompanied by fluctuation in levels of the endocannabinoid anandamide (AEA) in several brain structures including the amygdala, the hippocampus, the hypothalamus and the prefrontal cortex. Conversely, levels of 2-arachidonoyl-sn-glycerol were not significantly altered. Pharmacological inhibition of fatty acid amide hydrolase (FAAH), the enzyme responsible for the intracellular degradation of AEA, by URB597 (0.1 and 0.3 mg/kg, i.p.), reduced withdrawal-induced anxiety as assessed by the elevated plus maze test and the shock-probe defensive burying paradigm, but did not prevent the occurrence of somatic signs. Together, the results indicate that pharmacological strategies aimed at enhancing endocannabinoid signaling may offer therapeutic advantages to treat the negative affective state produced by nicotine withdrawal, which is critical for the maintenance of tobacco use.
url http://europepmc.org/articles/PMC3227620?pdf=render
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