F G Graeff

Summary

Country: Brazil

Publications

  1. ncbi The elevated T-maze as an experimental model of anxiety
    F G Graeff
    Laboratorio de Psicofarmacologia, FFCLRP e Núcleo de Neurociências e Comportamento da Universidade de São Paulo, Ribeirao Preto, Brazil
    Neurosci Biobehav Rev 23:237-46. 1998
  2. ncbi Escitalopram prolonged fear induced by simulated public speaking and released hypothalamic-pituitary-adrenal axis activation
    C Garcia-Leal
    Department of Neurology, Psychiatry and Medical Psychology, Medical School of Ribeirao Preto, University of Sao Paulo, Ribeirao Preto, SP, Brazil
    J Psychopharmacol 24:683-94. 2010
  3. ncbi Serotonergic regulation of inhibitory avoidance and one-way escape in the rat elevated T-maze
    H Zangrossi
    Department of Pharmacology, School of Medicine, University of Sao Paulo, 14049 901, SP, Ribeirao Preto, Brazil
    Neurosci Biobehav Rev 25:637-45. 2001
  4. ncbi Role of 5-HT in stress, anxiety, and depression
    F G Graeff
    Laboratorio de Psicofarmacologia, FFCLRP, Universidade de Sao Paulo, Ribeirao Preto, Brasil
    Pharmacol Biochem Behav 54:129-41. 1996
  5. ncbi Comparison between two models of experimental anxiety in healthy volunteers and panic disorder patients
    F G Graeff
    Department of Neurology, Psychiatry and Medical Psychology, Faculty of Medicine of Ribeirao Preto, University of Sao Paulo, 14049 900, SP, Ribeirao Preto, Brazil
    Neurosci Biobehav Rev 25:753-9. 2001
  6. ncbi Anxiolytic and panicolytic effects of escitalopram in the elevated T-maze
    S N Pinheiro
    Division of Psychiatry, School of Medicine of Ribeirao Preto, University of Sao Paulo, Ribeirao Preto, SP, Brazil
    J Psychopharmacol 22:132-7. 2008

Collaborators

Detail Information

Publications6

  1. ncbi The elevated T-maze as an experimental model of anxiety
    F G Graeff
    Laboratorio de Psicofarmacologia, FFCLRP e Núcleo de Neurociências e Comportamento da Universidade de São Paulo, Ribeirao Preto, Brazil
    Neurosci Biobehav Rev 23:237-46. 1998
    ..These behavioral and pharmacological results support the view that inhibitory avoidance in the elevated T-maze may be related to generalized anxiety disorder, while one-way escape may be associated with panic disorder...
  2. ncbi Escitalopram prolonged fear induced by simulated public speaking and released hypothalamic-pituitary-adrenal axis activation
    C Garcia-Leal
    Department of Neurology, Psychiatry and Medical Psychology, Medical School of Ribeirao Preto, University of Sao Paulo, Ribeirao Preto, SP, Brazil
    J Psychopharmacol 24:683-94. 2010
    ....
  3. ncbi Serotonergic regulation of inhibitory avoidance and one-way escape in the rat elevated T-maze
    H Zangrossi
    Department of Pharmacology, School of Medicine, University of Sao Paulo, 14049 901, SP, Ribeirao Preto, Brazil
    Neurosci Biobehav Rev 25:637-45. 2001
    ..Taken together, these results suggest that 5-HT exerts differential control on inhibitory avoidance and escape response in the elevated T-maze, mobilizing different types of 5-HT receptors in key structures implicated in fear/anxiety...
  4. ncbi Role of 5-HT in stress, anxiety, and depression
    F G Graeff
    Laboratorio de Psicofarmacologia, FFCLRP, Universidade de Sao Paulo, Ribeirao Preto, Brasil
    Pharmacol Biochem Behav 54:129-41. 1996
    ..Clinical implications of these results are discussed, especially with regard to panic disorder and depression...
  5. ncbi Comparison between two models of experimental anxiety in healthy volunteers and panic disorder patients
    F G Graeff
    Department of Neurology, Psychiatry and Medical Psychology, Faculty of Medicine of Ribeirao Preto, University of Sao Paulo, 14049 900, SP, Ribeirao Preto, Brazil
    Neurosci Biobehav Rev 25:753-9. 2001
    ..Therefore, panic patients seem to process unconditioned fear abnormally, which may be due to lack of 5-HT inhibition in brain structures commanding flight from proximal danger stimuli...
  6. ncbi Anxiolytic and panicolytic effects of escitalopram in the elevated T-maze
    S N Pinheiro
    Division of Psychiatry, School of Medicine of Ribeirao Preto, University of Sao Paulo, Ribeirao Preto, SP, Brazil
    J Psychopharmacol 22:132-7. 2008
    ..Since no such effect was observed following subchronic administration, it is likely that the mechanisms of the early and late anxiolytic actions of escitalopram are different...