Use of antidepressant drugs in the treatment of anxiety disorders has recently increased due to the anxiolytic effect of some of these agents. Because dopaminergic transmission in the prefrontal cortex is sensitive to anxiogenic or stressful stimuli, the effects of two antidepressant drugs with different mechanisms of action, imipramine and mirtazapine, on the response of rat cortical dopaminergic neurons to stress were investigated. A 2-week (but not single dose) administration of imipramine (10 mg/kg, i.p., twice daily) or mirtazapine (10 mg/kg, i.p., once daily) reduced and completely antagonized, respectively, the increase in dopamine release in the prefrontal cortex elicited by footshock stress. Long-term administration of imipramine or mirtazapine had no marked effect on the stress-induced increases in the brain or plasma concentrations of neuroactive steroids or corticosterone. An attenuation of the response of mesocortical dopaminergic neurons to stress induced by long-term treatment with antidepressants might contribute to the anxiolytic effects of such drugs. © 2001 Elsevier Science B.V. All rights reserved.

Prevention of the stress-induced increase in frontal cortical dopamine efflux of freely moving rats by long-term treatment with antidepressant drugs

Ma;Pisu;
2001

Abstract

Use of antidepressant drugs in the treatment of anxiety disorders has recently increased due to the anxiolytic effect of some of these agents. Because dopaminergic transmission in the prefrontal cortex is sensitive to anxiogenic or stressful stimuli, the effects of two antidepressant drugs with different mechanisms of action, imipramine and mirtazapine, on the response of rat cortical dopaminergic neurons to stress were investigated. A 2-week (but not single dose) administration of imipramine (10 mg/kg, i.p., twice daily) or mirtazapine (10 mg/kg, i.p., once daily) reduced and completely antagonized, respectively, the increase in dopamine release in the prefrontal cortex elicited by footshock stress. Long-term administration of imipramine or mirtazapine had no marked effect on the stress-induced increases in the brain or plasma concentrations of neuroactive steroids or corticosterone. An attenuation of the response of mesocortical dopaminergic neurons to stress induced by long-term treatment with antidepressants might contribute to the anxiolytic effects of such drugs. © 2001 Elsevier Science B.V. All rights reserved.
2001
antidepressant agent
corticosterone
dopamine
imipramine
mirtazapine
neurosteroid
animal experiment
animal tissue
anxiety neurosis
article
brain level
controlled study
corticosterone blood level
dopamine release
dopaminergic nerve cell
dopaminergic transmission
dose response
drug activity
drug effect
drug mechanism
long term care
male
nonhuman
prefrontal cortex
priority journal
rat
shock
steroid blood level
stimulation
stress
tranquilizing activity
Animals
Antidepressive Agents
Antidepressive Agents
Tricyclic
Dopamine
Electroshock
Extracellular Space
Frontal Lobe
Imipramine
Male
Mianserin
Microdialysis
Pregnenolone
Progesterone
Rats
Rats
Sprague-Dawley
Serotonin Uptake Inhibitors
Steroids
Stress
Psychological
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/198730
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