Subacute fluoxetine enhances conditioned responding and conditioning-specific reflex modification of the rabbit nictitating membrane response: implications for drug treatment with selective serotonin reuptake inhibitors

被引:8
|
作者
Burhans, Lauren B. [1 ]
Smith-Bell, Carrie A. [1 ]
Schreurs, Bernard G. [1 ]
机构
[1] W Virginia Univ, Dept Physiol & Pharmacol, Hlth Sci Ctr, Blanchette Rockefeller Neurosci Inst, Morgantown, WV 26506 USA
来源
BEHAVIOURAL PHARMACOLOGY | 2013年 / 24卷 / 01期
关键词
classical conditioning; eyeblink; fear conditioning; fluoxetine; nictitating membrane response; post-traumatic stress disorder; rabbit; selective serotonin reuptake inhibitor; 5-HT2A RECEPTOR; PHARMACOLOGICAL-TREATMENT; CENTRAL NUCLEUS; WATER MAZE; AMYGDALA; FEAR; ACQUISITION; EXTINCTION; ANXIETY; CORTEX;
D O I
10.1097/FBP.0b013e32835d528e
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Extensive research on the rabbit nictitating membrane response (NMR) has shown that the NMR reflex can become exaggerated following classical fear conditioning. This learning-related change is referred to as conditioning-specific reflex modification (CRM) and is observed in the absence of the conditioned stimulus. The aim of the current study was to examine the sensitivity of the CRM paradigm to serotonergic manipulation with fluoxetine, a commonly prescribed selective serotonin reuptake inhibitor for anxiety disorders. To assess the effect of fluoxetine on exaggerated reflexive responding indicative of CRM and on conditioned cued fear, rabbits underwent delay NMR conditioning (pairings of tone and periorbital shock) and were tested for CRM, followed by 5 days of daily fluoxetine (0.03, 0.3, or 3.0 mg/kg) or saline injections. CRM was reassessed 1 day and 1 week later, followed by a retention test of conditioned responses (CRs) to the tone. Fluoxetine (3.0 mg/kg) enhanced CRM and retention of conditioned responses, a week after treatment ceased, and this is in agreement with the reports on increased anxiety-like behaviors in other animal models and humans. The CRM paradigm, therefore, may provide important insight into the mechanisms underlying the paradoxical selective serotonin reuptake inhibitor effects. Behavioural Pharmacology 24: 55-64 (C) 2013 Wolters Kluwer Health | Lippincott Williams & Wilkins.
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页码:55 / 64
页数:10
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