On Disruption of Fear Memory by Reconsolidation Blockade: Evidence from Cannabidiol Treatment


Autoria(s): Stern, Cristina A. J.; Gazarini, Lucas; Takahashi, Reinaldo N.; Guimaraes, Francisco S.; Bertoglio, Leandro J.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

23/10/2013

23/10/2013

2012

Resumo

The search for reconsolidation blockers may uncover clinically relevant drugs for disrupting memories of significant stressful life experiences, such as those underlying the posttraumatic stress disorder. Considering the safety of systemically administered cannabidiol (CBD), the major non-psychotomimetic component of Cannabis sativa, to animals and humans, the present study sought to investigate whether and how this phytocannabinoid (3-30 mg/kg intraperitoneally; i.p.) could mitigate an established memory, by blockade of its reconsolidation, evaluated in a contextual fear-conditioning paradigm in rats. We report that CBD is able to disrupt 1- and 7-days-old memories when administered immediately, but not 6 h, after their retrieval for 3 min, with the dose of 10 mg/kg being the most effective. This effect persists in either case for at least 1 week, but is prevented when memory reactivation was omitted, or when the cannabinoid type-1 receptors were antagonized selectively with AM251 (1.0 mg/kg). Pretreatment with the serotonin type-1A receptor antagonist WAY100635, however, failed to block CBD effects. These results highlight that recent and older fear memories are equally vulnerable to disruption induced by CBD through reconsolidation blockade, with a consequent long-lasting relief in contextual fear-induced freezing. Importantly, this CBD effect is dependent on memory reactivation, restricted to time window of <6h, and is possibly dependent on cannabinoid type-1 receptor-mediated signaling mechanisms. We also observed that the fear memories disrupted by CBD treatment do not show reinstatement or spontaneous recovery over 22 days. These findings support the view that reconsolidation blockade, rather than facilitated extinction, accounts for the aforementioned CBD results in our experimental conditions. Neuropsychopharmacology (2012) 37, 2132-2142; doi:10.1038/npp.2012.63; published online 2 May 2012

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo

Fundacao de Amparo a Pesquisa do Estado de Sao Paulo [07/03685-3]

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico [308457/2008-0, 480903/2010-7]

Conselho Nacional de Desenvolvimento Cientifico e Tecnologico

Identificador

NEUROPSYCHOPHARMACOLOGY, LONDON, v. 37, n. 9, supl. 4, Part 1-2, pp. 2132-2142, AUG, 2012

0893-133X

http://www.producao.usp.br/handle/BDPI/35692

10.1038/npp.2012.63

http://dx.doi.org/10.1038/npp.2012.63

Idioma(s)

eng

Publicador

NATURE PUBLISHING GROUP

LONDON

Relação

NEUROPSYCHOPHARMACOLOGY

Direitos

restrictedAccess

Copyright NATURE PUBLISHING GROUP

Palavras-Chave #FEAR MEMORY #RECONSOLIDATION BLOCKADE #CANNABIDIOL #MIDAZOLAM #FEAR EXTINCTION #VENTROMEDIAL PREFRONTAL CORTEX #PROTEIN-SYNTHESIS #5-HT1A RECEPTORS #CB1 RECEPTORS #IN-VIVO #EXTINCTION #AMYGDALA #REACTIVATION #CONSOLIDATION #ACTIVATION #NEUROSCIENCES #PHARMACOLOGY & PHARMACY #PSYCHIATRY
Tipo

article

original article

publishedVersion