THE ANTERIOR CINGULATE CORTEX IS A TARGET STRUCTURE FOR THE ANXIOLYTIC-LIKE EFFECTS OF BENZODIAZEPINES ASSESSED BY REPEATED EXPOSURE TO THE ELEVATED PLUS MAZE AND FOS IMMUNOREACTIVITY


Autoria(s): ALBRECHET-SOUZA, L.; BORELLI, K. G.; CARVALHO, M. C.; BRANDAO, M. L.
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

19/10/2012

19/10/2012

2009

Resumo

Prior experience with the elevated plus maze (EPM) increases the avoidance of rodents to the open arms and impairs the anxiolytic-like effects of benzodiazepines on the traditional behaviors evaluated upon re-exposure to the maze, a phenomenon known as one-trial tolerance. Risk assessment behaviors are also sensitive to benzodiazepines. During re-exposure to the maze, these behaviors reinstate the information-processing initiated during the first experience, and the detection of danger generates stronger open-arm avoidance. The present study investigated whether the benzodiazepine midazolam alters risk assessment behaviors and Fos protein distribution associated with test and retest sessions in the EPM. Naive or maze-experienced Wistar rats received either saline or midazolam (0.5 mg/kg i.p.) and were subjected to the EPM. Midazolam caused the usual effects on exploratory behavior, increasing exploratory activity of naive rats in the open arms and producing no effects on these conventional measures in rats re-exposed to the maze. Risk assessment behaviors, however, were sensitive to the benzodiazepine during both sessions, indicating anxiolytic-like effects of the drug in both conditions. Fos immunohistochemistry showed that midazolam injections were associated with a distinct pattern of action when administered before the test or retest session, and the anterior cingulate cortex, area 1 (Cg1), was the only structure targeted by the benzodiazepine in both situations. Bilateral infusions of midazolam into the Cg1 replicated the behavioral effects of the drug injected systemically, suggesting that this area is critically involved in the anxiolytic-like effects of benzodiazepines, although the behavioral strategy adopted by the animals appears to depend on the previous knowledge of the threatening environment. (C) 2009 IBRO. Published by Elsevier Ltd. All rights reserved.

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo[2006/06354-5]

FAPESP Fundacao de Amparo a Pesquisa do Estado de Sao Paulo[061514554]

CNPq[20071472030]

CNPq Conselho Nacional de Desenvolvimento Cientifico e Tecnologico

CAPES Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Identificador

NEUROSCIENCE, v.164, n.2, p.387-397, 2009

0306-4522

http://producao.usp.br/handle/BDPI/20895

10.1016/j.neuroscience.2009.08.038

http://dx.doi.org/10.1016/j.neuroscience.2009.08.038

Idioma(s)

eng

Publicador

PERGAMON-ELSEVIER SCIENCE LTD

Relação

Neuroscience

Direitos

restrictedAccess

Copyright PERGAMON-ELSEVIER SCIENCE LTD

Palavras-Chave #defensive behavior #anxiety #midazolam #cingulate cortex 1 #Fos expression #ONE-TRIAL TOLERANCE #MEDIAL PREFRONTAL CORTEX #DORSAL PREMAMMILLARY NUCLEUS #PERIAQUEDUCTAL GRAY #CONDITIONED FEAR #ELECTRICAL-STIMULATION #RAPHE NUCLEUS #RAT-BRAIN #AUTORADIOGRAPHIC LOCALIZATION #ETHOPHARMACOLOGICAL ANALYSIS #Neurosciences
Tipo

article

original article

publishedVersion