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Dorsal periaqueductal gray stimulation facilitates anxiety-, but not panic-related, defensive responses in rats tested in the elevated T-maze
Camplesi Jr, M.; Bortoli, V.C.de; Soares, V. de Paula; Nogueira, R.L.; Zangrossi Jr., H..
  • Camplesi Jr, M.; Universidade Federal de Goiás. Instituto de Patologia Tropical e Saúde Pública. Goiânia. BR
  • Bortoli, V.C.de; Universidade Federal do Espírito Santo. Centro Universitário Norte do Espírito Santo. Departamento de Ciências da Saúde. São Mateus. BR
  • Soares, V. de Paula; Universidade Federal do Rio Grande do Norte. Centro de Biociências. Departamento de Biofísica e Farmacologia. Natal. BR
  • Nogueira, R.L.; Universidade Estácio de Sá. Laboratório de Psicologia Comparada. Rio de Janeiro. BR
  • Zangrossi Jr., H.; Universidade de São Paulo. Faculdade de Medicina de Ribeirão Preto. Departamento de Farmacologia. Ribeirão Preto. BR
Braz. j. med. biol. res ; 45(11): 1025-1030, Nov. 2012. ilus, tab
Article Dans Anglais | LILACS | ID: lil-650579
ABSTRACT
The escape response to electrical or chemical stimulation of the dorsal periaqueductal gray matter (DPAG) has been associated with panic attacks. In order to explore the validity of the DPAG stimulation model for the study of panic disorder, we determined if the aversive consequences of the electrical or chemical stimulation of this midbrain area can be detected subsequently in the elevated T-maze. This animal model, derived from the elevated plus-maze, permits the measurement in the same rat of a generalized anxiety- and a panic-related defensive response, i.e., inhibitory avoidance and escape, respectively. Facilitation of inhibitory avoidance, suggesting an anxiogenic effect, was detected in male Wistar rats (200-220 g) tested in the elevated T-maze 30 min after DPAG electrical stimulation (current generated by a sine-wave stimulator, frequency at 60 Hz) or after local microinjection of the GABA A receptor antagonist bicuculline (5 pmol). Previous electrical (5, 15, 30 min, or 24 h before testing) or chemical stimulation of this midbrain area did not affect escape performance in the elevated T-maze or locomotion in an open-field. No change in the two behavioral tasks measured by the elevated T-maze was observed after repetitive (3 trials) electrical stimulation of the DPAG. The results indicate that activation of the DPAG caused a short-lived, but selective, increase in defensive behaviors associated with generalized anxiety.
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Texte intégral: Disponible Indice: LILAS (Amériques) Sujet Principal: Anxiété / Comportement animal / Substance grise centrale du mésencéphale / Trouble panique / Réaction de fuite Limites du sujet: Animaux langue: Anglais Texte intégral: Braz. j. med. biol. res Thème du journal: Biologie / Médicament Année: 2012 Type: Article Pays d'affiliation: Brésil Institution/Pays d'affiliation: Universidade Estácio de Sá/BR / Universidade Federal de Goiás/BR / Universidade Federal do Espírito Santo/BR / Universidade Federal do Rio Grande do Norte/BR / Universidade de São Paulo/BR

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Texte intégral: Disponible Indice: LILAS (Amériques) Sujet Principal: Anxiété / Comportement animal / Substance grise centrale du mésencéphale / Trouble panique / Réaction de fuite Limites du sujet: Animaux langue: Anglais Texte intégral: Braz. j. med. biol. res Thème du journal: Biologie / Médicament Année: 2012 Type: Article Pays d'affiliation: Brésil Institution/Pays d'affiliation: Universidade Estácio de Sá/BR / Universidade Federal de Goiás/BR / Universidade Federal do Espírito Santo/BR / Universidade Federal do Rio Grande do Norte/BR / Universidade de São Paulo/BR