Reversal of startle gating deficits in transgenic mice overexpressing corticotropin-releasing factor by antipsychotic drugs

Autor: Lucianne Groenink, Jocelien D A Olivier, Mark A. Geyer, Berend Olivier, Jan van der Gugten, P. Monika Verdouw, Anneloes Dirks, Koen G.C. Westphal
Přispěvatelé: Groningen Institute for Evolutionary Life Sciences, Olivier lab
Jazyk: angličtina
Rok vydání: 2003
Předmět:
Male
Startle response
Reflex
Startle

Inhibition (Psychology)
Corticotropin-Releasing Hormone
medicine.medical_treatment
Inbred Strains
Gating
Transgenic
Mice
Haloperidol
Prepulse inhibition
Clozapine
medicine.diagnostic_test
Behavior
Animal

Depression
Startle
Stimulation
Chemical

Psychiatry and Mental health
Inhibition
Psychological

Drug
Psychology
hormones
hormone substitutes
and hormone antagonists

medicine.drug
Antipsychotic Agents
medicine.medical_specialty
endocrine system
medicine.drug_class
Atypical antipsychotic
Mice
Inbred Strains

Mice
Transgenic

Chemical
Dose-Response Relationship
Cognitive neurosciences [UMCN 3.2]
Internal medicine
Reflex
medicine
Animals
Acoustic
Antipsychotic
Pharmacology
Behavior
Dose-Response Relationship
Drug

Animal
Body Weight
Typical antipsychotic
Reflex
Acoustic

Disease Models
Animal

Endocrinology
Acoustic Stimulation
Disease Models
Stimulation
Zdroj: Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology, 28(10), 1790-1798. Nature Publishing Group
Neuropsychopharmacology, 28, 1790-8
Neuropsychopharmacology, 28, 10, pp. 1790-8
ISSN: 0893-133x
0893-133X
Popis: Item does not contain fulltext Chronically elevated levels of corticotropin-releasing factor (CRF) in transgenic mice overexpressing CRF in the brain (CRF-OE) appear to be associated with alterations commonly associated with major depressive disorder, as well as with sensorimotor gating deficits commonly associated with schizophrenia. In the present study, we tested the hypothesis that antipsychotics may be effective in normalizing prepulse inhibition (PPI) of acoustic startle in CRF-OE mice, which display impaired sensorimotor gating compared to wild-type (WT) mice. The typical antipsychotic haloperidol and atypical antipsychotic risperidone improved PPI in the CRF-OE mice, but were ineffective in WT mice. The atypical antipsychotic clozapine did not influence PPI in CRF-OE mice, but reduced gating in WT mice. This effect of clozapine in the CRF-OE mice may thus be regarded as a relative improvement, consistent with the observed effect of haloperidol and risperidone. As expected, the anxiolytic, nonantipsychotic chlordiazepoxide was devoid of any effect. All four compounds dose-dependently reduced the acoustic startle response irrespective of genotype. These results indicate that antipsychotic drugs are effective in improving startle gating deficits in the CRF-OE mice. Hence, the CRF-OE mouse model may represent an animal model for certain aspects of psychotic depression, and could be a valuable tool for research addressing the impact of chronically elevated levels of CRF on information processing.
Databáze: OpenAIRE