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[The psychological stress model using motor suppression].

H Kamei1, Y Noda, T Nabeshima

  • 1Department of Neuropsychopharmacology & Hospital Pharmacy, Nagoya University School of Medicine, Japan.

Nihon Yakurigaku Zasshi. Folia Pharmacologica Japonica
|April 17, 1999
PubMed
Summary

Psychological stress causes motor suppression in mice, a model for affective disorders. Sigma receptor agonists, not typical anxiolytics, reduced this conditioned fear stress response.

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Area of Science:

  • Neuroscience
  • Behavioral Science
  • Psychopharmacology

Background:

  • Psychological stress is linked to anxiety and depression.
  • Existing research focuses on physiological stressors, with limited data on psychological stress behaviors.
  • Motor suppression is a known response to stressors like footshock in animal models.

Purpose of the Study:

  • To investigate behavioral changes in psychological stress using a conditioned fear stress (CFS) model.
  • To characterize motor suppression as a conditioned emotional response.
  • To evaluate the efficacy of sigma receptor agonists and standard anxiolytics/antidepressants in the CFS model.

Main Methods:

  • Inducing conditioned fear stress (CFS) in mice by re-exposure to a footshock environment.

Related Experiment Videos

  • Measuring motor suppression as a behavioral outcome.
  • Administering sigma receptor agonists ((+)-N-allylnormetazocine, dextromethorphan) and comparing their effects to anxiolytics (diazepam, chlordiazepoxide) and antidepressants (imipramine, fluoxetine).
  • Main Results:

    • Mice displayed significant motor suppression when placed in the CFS environment.
    • Sigma receptor agonists markedly attenuated the motor suppression.
    • Typical anxiolytics and antidepressants showed no significant effect on CFS-induced motor suppression.

    Conclusions:

    • The conditioned fear stress (CFS) model effectively demonstrates psychological stress-induced motor suppression.
    • This model may be valuable for studying the pathogenesis of affective disorders, especially treatment-resistant forms.
    • Sigma receptor agonists show potential as novel therapeutic agents for stress-related affective disorders.