Short- and long-term anxiogenic effects induced by a single injection of subconvulsant doses of pilocarpine in rats: investigation of the putative role of hippocampal pathways


Autoria(s): DUARTE, Filipe Silveira; GAVIOLI, Elaine Cristina; DUZZIONI, Marcelo; HOELLER, Alexandre Ademar; CANTERAS, Newton Sabino; LIMA, Thereza Christina Monteiro De
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2010

Resumo

Behavioral consequences of convulsive episodes are well documented, but less attention was paid to changes that occur in response to subconvulsant doses of drugs. We investigated short- and long-term effects of a single systemic injection of a subconvulsant dose of pilocarpine on the behavior of rats as evaluated in the elevated plus maze. Pilocarpine induced an anxiogenic-like profile 24 h later, and this effect persisted for up to 3 months (% of time spent on open arms at 24 h, control = 35.47 +/- 3.23; pilocarpine 150 = 8.2 +/- 2.6; 3 months, control = 31.9 +/- 5.5; pilocarpine 150 = 9.3 +/- 4.9). Temporary inactivation of fimbria-fornix with lidocaine 4% promoted an anxiolytic-like effect per se, suggesting a tonic control of this pathway on the modulation of anxiety-related behaviors. Lidocaine also reduced the anxiogenic-like profile of animals tested 1 month after pilocarpine treatment (% of time spent on open arms, saline + phosphate-buffered saline (PBS) = 31.7 + 3.7; saline + lidocaine = 54.4 + 4.7; pilocarpine + PBS = 10.3 + 4.1; pilocarpine + lidocaine = 40.1 + 9.1). To determine whether the anxiogenic-like effect was mediated by septal region or by direct hippocampal projections to the diencephalon, the neural transmission of post-commissural fornix was blocked, and a similar reduction in the anxiogenic-like effect of pilocarpine was observed. Our findings suggest that a single systemic injection of pilocarpine may induce long-lasting anxiogenic-like behavior in rats, an effect that appears to be mediated, in part, through a direct path from hippocampus to medial hypothalamic sites involved in fear responses.

Brazilian National Research Council (CNPq)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CAPES

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

CNPq

Identificador

PSYCHOPHARMACOLOGY, v.212, n.4, p.653-661, 2010

0033-3158

http://producao.usp.br/handle/BDPI/27838

10.1007/s00213-010-1985-6

http://dx.doi.org/10.1007/s00213-010-1985-6

Idioma(s)

eng

Publicador

SPRINGER

Relação

Psychopharmacology

Direitos

restrictedAccess

Copyright SPRINGER

Palavras-Chave #Pilocarpine #Fear #Anxiety #Hippocampus #Fimbria-fornix #Post-commissural fornix #Elevated plus maze #SPONTANEOUS RECURRENT SEIZURES #INDUCED STATUS EPILEPTICUS #TEMPORAL-LOBE EPILEPSY #ELEVATED PLUS-MAZE #ACETYLCHOLINE-RELEASE #EXTRACELLULAR ACETYLCHOLINE #VENTRAL SUBICULUM #IN-VITRO #ANXIETY #AMYGDALA #Neurosciences #Pharmacology & Pharmacy #Psychiatry
Tipo

article

original article

publishedVersion