Altered behavioural response to acute stress in mice lacking cellular prion protein

Autor(es):Mostrar menos -

Nico‚ P.B.C. ; de-Paris‚ F. ; Vinadé‚ E.R. ; Amaral‚ O.B. ; Rockenbach‚ I. ; Soares‚ B.L. ; Guarnieri‚ R. ; Wichert-Ana‚ L. ; Calvo‚ F. ; Walz‚ R. ; others

• Tipo de documento: Artigo Científico
• Fonte: Behavioural Brain Research; v. 162, n. 2, p. 173-181, 2005.

Resumo

Although many studies have investigated the function of cellular prion protein (PrPc), its physiologic role remains elusive. PrPc null mice have been reported to develop normally and to show normal performance in most behavioural tests. In the present study we investigated whether this also holds true after episodes of acute stress. PtPc gene ablated (Prnp(0/0)) and wild-type mice were subjected to restraint stress, electric foot shock. or swimming and compared with non-stressed animals. Immediately after the stressful situation, the anxiety levels and locomotion of the animals were measured using plus-maze and open-field tests. Among non-stressed animals, there was no significant difference in performance between Prnp(0/0) and wild type animals in either test. However, after acute stress provoked by a foot shock or a swimming trial, Prnp(0/0) animals showed a significant decrease in anxiety levels when compared with control animals. Moreover, after the swimming test, knockout mice presented decreased locomotion when compared to wild-type mice. Because of this observation, we also assessed both types of mice in a forced swimming test with the objective of better evaluating muscle function and found that Prn(0/0) animals presented reduced forced swimming capacity when compared to controls. As far as we know, this is the first report suggesting that cellular prion protein is involved in modulation of anxiety or muscular activity after acute psychic or physical stress. (c) 2005 Elsevier B.V. All rights reserved. (AU)

• Processo FAPESP: 02/03743-0 - Pesquisa de novos marcadores eletrofisiológicos ictais e interictais para o diagnóstico e prognóstico de pacientes com epilepsias focais do lobo temporal refratárias ao tratamento clínico
• Beneficiário: Marino Muxfeldt Bianchin
• Modalidade de apoio: Bolsas no Brasil - Pós-Doutorado
• Processo FAPESP: 03/13189-2 - Papel da proteína prion celular em processos fisiológicos e patológicos II
• Beneficiário: Vilma Regina Martins
• Modalidade de apoio: Auxílio à Pesquisa - Temático