L-NOARG-induced catalepsy can be influenced by glutamatergic neurotransmission mediated by NMDA receptors in the inferior colliculus

Autor(es)

Iacopucci, A. P. ^[1] ; Mello, R. O. ^[1] ; Barbosa-Silva, R. ^{[2, 3]} ; Melo-Thomas, L. ^{[2, 3]}

Afiliação do(s) autor(es)

^[1] Univ Sao Francisco, Lab Neuropsicofarmacol, BR-12916900 Braganca Paulista, SP - Brazil

^[2] Univ Fed Sao Paulo, Dept Biociencias, BR-11060001 Santos, SP - Brazil

^[3] Inst Neurociencias & Comportamento INeC, BR-14040901 Ribeirao Preto, SP - Brazil

• Tipo de documento: Artigo Científico
• Fonte: Behavioural Brain Research; v. 234, n. 2, p. 149-154, OCT 1 2012.
• Citações Web of Science: 7

Resumo

The inferior colliculus (IC), a midbrain structure that processes acoustic information of aversive nature, is distinguished from other auditory nuclei in the brainstem by its connections with structures of the motor system. Recent evidence relating the IC to motor behavior shows that glutamate-mediated mechanisms in the neural circuits at the IC level modulate haloperidol-induced catalepsy. It has been shown that N-G-nitro-L-arginine (L-NOARG), inhibitor of enzyme nitric oxide synthase (NOS), can induce catalepsy after intraperitoneal (ip), intracerebroventricular or intrastriatal administration. The present study examined whether the catalepsy induced by L-NOARG (ip) can be influenced by collicular glutamatergic mechanisms and if a NO-dependent neural substrate into the IC plays a role in this immobility state. L-NOARG-induced catalepsy was challenged with prior intracollicular microinjections of glutamate NMDA receptor antagonists, AP7 (20 or 40 nmo1/0.5 mu l), or of the NMDA receptor agonist N-methyl-D-aspartate (NMDA, 30 nmo1/0.5 mu l). Catalepsy was evaluated by positioning both forepaws of the rats on an elevated horizontal wooden bar and recording the time for which the animal maintained this position. The results showed that intracollicular microinjection of AP7 previous to systemic injections of L-NOARG (90 mg/kg) significantly attenuated the catalepsy. Conversely, intracollicular microinjection of NMDA increased the time of catalepsy when administered 10 min before systemic L-NOARG (10 or 45 mg/kg). The microinjection of L-NOARG (50 or 100 nmol) directly into the IC was not able to induce catalepsy. These findings suggest that glutamate-mediated mechanisms in the neural circuits of the IC modulate L-NOARG-induced catalepsy and participate in the regulation of motor activity. (C) 2012 Elsevier B.V. All rights reserved. (AU)

• Processo FAPESP: 09/01437-8 - Estudo da neurotransmissão glutamatérgica mediada por receptores NMDA no colículo inferior sobre a catalepsia induzida pelo haloperidol
• Beneficiário: Liana Melo-Thomas
• Modalidade de apoio: Auxílio à Pesquisa - Regular