Effects of psychotropic agents on extinction of lever-press avoidance in a rat model of anxiety vulnerability
Avoidance and its perseveration represent key features of anxiety disorders. Both pharmacological and behavioral approaches (i.e. anxiolytics and extinction therapy) have been utilized to modulate avoidance behavior in patients. However, the outcome has not always been desirable. Part of the reason...
| Main Authors: | , , , , , , |
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| Format: | Article |
| Language: | English |
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Frontiers Media S.A.
2014-09-01
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| Series: | Frontiers in Behavioral Neuroscience |
| Subjects: | |
| Online Access: | http://journal.frontiersin.org/Journal/10.3389/fnbeh.2014.00322/full |
| _version_ | 1819107923509379072 |
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| author | Xilu eJiao Xilu eJiao Xilu eJiao Kevin D. Beck Kevin D. Beck Kevin D. Beck Amanda L. Stewarts Ian M. Smith Ian M. Smith Catherine E. Myers Catherine E. Myers Catherine E. Myers Richard J Servatius Richard J Servatius Richard J Servatius Kevin C.H. Pang Kevin C.H. Pang Kevin C.H. Pang |
| author_facet | Xilu eJiao Xilu eJiao Xilu eJiao Kevin D. Beck Kevin D. Beck Kevin D. Beck Amanda L. Stewarts Ian M. Smith Ian M. Smith Catherine E. Myers Catherine E. Myers Catherine E. Myers Richard J Servatius Richard J Servatius Richard J Servatius Kevin C.H. Pang Kevin C.H. Pang Kevin C.H. Pang |
| author_sort | Xilu eJiao |
| collection | DOAJ |
| description | Avoidance and its perseveration represent key features of anxiety disorders. Both pharmacological and behavioral approaches (i.e. anxiolytics and extinction therapy) have been utilized to modulate avoidance behavior in patients. However, the outcome has not always been desirable. Part of the reason is attributed to the diverse neuropathology of anxiety disorders. Here, we investigated the effect of psychotropic drugs that target various monoamine systems on extinction of avoidance behavior using lever-press avoidance task. Here we used the Wistar-Kyoto (WKY) rat, a unique rat model that exhibits facilitated avoidance and extinction resistance along with malfunction of the dopamine (DA) system. Sprague Dawley (SD) and WKY rats were trained to acquire lever-press avoidance. WKY rats acquired avoidance faster and to a higher level compared to SD rats. During pharmacological treatment, bupropion, and desipramine significantly reduced avoidance response selectively in WKY rats. However, after the discontinuation of drug treatment, only those WKY rats that were previously treated with desipramine exhibited lower avoidance response compared to the control group. In contrast, none of the psychotropic drugs facilitated avoidance extinction in SD rats. Instead, desipramine impaired avoidance extinction and increased non-reinforced response in SD rats. Interestingly, paroxetine, a widely used antidepressant and anxiolytic, exhibited the weakest effect in WKY rats and no effects at all in SD rats. Thus, our data suggest that malfunctions in brain catecholamine system could be one of the underlying etiologies of anxiety-like behavior, particularly avoidance perseveration. Pharmacological manipulation targeting DA and norepinephrine is more effective to facilitate extinction learning in this strain. The data from the present study may shed light on new pharmacological approaches to treat patients with anxiety disorders who are not responding to serotonin re-uptake inhibitors. |
| first_indexed | 2024-12-22T03:01:45Z |
| format | Article |
| id | doaj.art-0df49bc75086457480d25d6ef4ddfa26 |
| institution | Directory Open Access Journal |
| issn | 1662-5153 |
| language | English |
| last_indexed | 2024-12-22T03:01:45Z |
| publishDate | 2014-09-01 |
| publisher | Frontiers Media S.A. |
| record_format | Article |
| series | Frontiers in Behavioral Neuroscience |
| spelling | doaj.art-0df49bc75086457480d25d6ef4ddfa262022-12-21T18:41:09ZengFrontiers Media S.A.Frontiers in Behavioral Neuroscience1662-51532014-09-01810.3389/fnbeh.2014.00322102697Effects of psychotropic agents on extinction of lever-press avoidance in a rat model of anxiety vulnerabilityXilu eJiao0Xilu eJiao1Xilu eJiao2Kevin D. Beck3Kevin D. Beck4Kevin D. Beck5Amanda L. Stewarts6Ian M. Smith7Ian M. Smith8Catherine E. Myers9Catherine E. Myers10Catherine E. Myers11Richard J Servatius12Richard J Servatius13Richard J Servatius14Kevin C.H. Pang15Kevin C.H. Pang16Kevin C.H. Pang17VA Medical CenterRutgers – New Jersey Medical SchoolVeterans Bio-Medical Research Institute (VBRI)VA Medical CenterRutgers – New Jersey Medical SchoolThe Sate University of New JerseyVeterans Bio-Medical Research Institute (VBRI)Rutgers – New Jersey Medical SchoolVeterans Bio-Medical Research Institute (VBRI)VA Medical CenterRutgers – New Jersey Medical SchoolThe Sate University of New JerseyVA Medical CenterRutgers – New Jersey Medical SchoolThe Sate University of New JerseyVA Medical CenterRutgers – New Jersey Medical SchoolThe Sate University of New JerseyAvoidance and its perseveration represent key features of anxiety disorders. Both pharmacological and behavioral approaches (i.e. anxiolytics and extinction therapy) have been utilized to modulate avoidance behavior in patients. However, the outcome has not always been desirable. Part of the reason is attributed to the diverse neuropathology of anxiety disorders. Here, we investigated the effect of psychotropic drugs that target various monoamine systems on extinction of avoidance behavior using lever-press avoidance task. Here we used the Wistar-Kyoto (WKY) rat, a unique rat model that exhibits facilitated avoidance and extinction resistance along with malfunction of the dopamine (DA) system. Sprague Dawley (SD) and WKY rats were trained to acquire lever-press avoidance. WKY rats acquired avoidance faster and to a higher level compared to SD rats. During pharmacological treatment, bupropion, and desipramine significantly reduced avoidance response selectively in WKY rats. However, after the discontinuation of drug treatment, only those WKY rats that were previously treated with desipramine exhibited lower avoidance response compared to the control group. In contrast, none of the psychotropic drugs facilitated avoidance extinction in SD rats. Instead, desipramine impaired avoidance extinction and increased non-reinforced response in SD rats. Interestingly, paroxetine, a widely used antidepressant and anxiolytic, exhibited the weakest effect in WKY rats and no effects at all in SD rats. Thus, our data suggest that malfunctions in brain catecholamine system could be one of the underlying etiologies of anxiety-like behavior, particularly avoidance perseveration. Pharmacological manipulation targeting DA and norepinephrine is more effective to facilitate extinction learning in this strain. The data from the present study may shed light on new pharmacological approaches to treat patients with anxiety disorders who are not responding to serotonin re-uptake inhibitors.http://journal.frontiersin.org/Journal/10.3389/fnbeh.2014.00322/fullDopamineNorepinephrineSerotoninanxiolyticbehavioral inhibitionavoidance perseveration |
| spellingShingle | Xilu eJiao Xilu eJiao Xilu eJiao Kevin D. Beck Kevin D. Beck Kevin D. Beck Amanda L. Stewarts Ian M. Smith Ian M. Smith Catherine E. Myers Catherine E. Myers Catherine E. Myers Richard J Servatius Richard J Servatius Richard J Servatius Kevin C.H. Pang Kevin C.H. Pang Kevin C.H. Pang Effects of psychotropic agents on extinction of lever-press avoidance in a rat model of anxiety vulnerability Frontiers in Behavioral Neuroscience Dopamine Norepinephrine Serotonin anxiolytic behavioral inhibition avoidance perseveration |
| title | Effects of psychotropic agents on extinction of lever-press avoidance in a rat model of anxiety vulnerability |
| title_full | Effects of psychotropic agents on extinction of lever-press avoidance in a rat model of anxiety vulnerability |
| title_fullStr | Effects of psychotropic agents on extinction of lever-press avoidance in a rat model of anxiety vulnerability |
| title_full_unstemmed | Effects of psychotropic agents on extinction of lever-press avoidance in a rat model of anxiety vulnerability |
| title_short | Effects of psychotropic agents on extinction of lever-press avoidance in a rat model of anxiety vulnerability |
| title_sort | effects of psychotropic agents on extinction of lever press avoidance in a rat model of anxiety vulnerability |
| topic | Dopamine Norepinephrine Serotonin anxiolytic behavioral inhibition avoidance perseveration |
| url | http://journal.frontiersin.org/Journal/10.3389/fnbeh.2014.00322/full |
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