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VPAC2 receptor activation mediates VIP enhancement of population spikes in the CA1 area of the hippocampus

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Detalhes bibliográficos
Resumo:The receptors mediating vasoactive intestinal polypeptide (VIP) enhancement of synaptic transmission to pyramidal cell bodies were investigated. RO 25–1553 (VPAC2 agonist) mimicked the excitatory effect of VIP on population spike (PS) amplitude. [K15, R16, L27]VIP (1–7)/GRF (8–27) (VPAC1 agonist) caused only a small increase in PS amplitude. The effect ofVPAC2 agonist (but not of theVPAC1 agonist)persisted upon blockade of GABAergic transmission and was strongly attenuated upon inhibition of PKA. In conclusion, VPAC2 receptor activation mediates VIP enhancement of PS amplitude in the hippocampus essentially through a PKA-dependent mechanism.
Autores principais:Cunha-Reis, Diana
Outros Autores:Ribeiro, Joaquim A.; Sebastião, Ana M
Assunto:VIP VPAC1 VPAC2 PKA PKC Hippocampus
Ano:2006
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso restrito
Instituição associada:Universidade de Lisboa
Idioma:inglês
Origem:Repositório da Universidade de Lisboa
Descrição
Resumo:The receptors mediating vasoactive intestinal polypeptide (VIP) enhancement of synaptic transmission to pyramidal cell bodies were investigated. RO 25–1553 (VPAC2 agonist) mimicked the excitatory effect of VIP on population spike (PS) amplitude. [K15, R16, L27]VIP (1–7)/GRF (8–27) (VPAC1 agonist) caused only a small increase in PS amplitude. The effect ofVPAC2 agonist (but not of theVPAC1 agonist)persisted upon blockade of GABAergic transmission and was strongly attenuated upon inhibition of PKA. In conclusion, VPAC2 receptor activation mediates VIP enhancement of PS amplitude in the hippocampus essentially through a PKA-dependent mechanism.