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Neurobiol Learn Mem ; 136: 189-195, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27773594

ABSTRACT

Selective serotonin reuptake inhibitors (SSRIs) are widely prescribed to treat anxiety and depression, yet they paradoxically increase anxiety during initial treatment. Acute administration of these drugs prior to learning can also enhance Pavlovian cued fear conditioning. This potentiation has been previously reported to depend upon the bed nucleus of the stria terminalis (BNST). Here, using temporary inactivation, we confirmed that the BNST is not necessary for the acquisition of cued or contextual fear memory. Systemic administration of the SSRI citalopram prior to fear conditioning led to an upregulation of the immediate early gene Arc (activity-regulated cytoskeleton-associated protein) in the oval nucleus of the BNST, and a majority of these neurons expressed the 5-HT2C receptor. Finally, local infusions of a 5-HT2C receptor antagonist directly into the oval nucleus of the BNST prevented the fear memory-enhancing effects of citalopram. These findings highlight the ability of the BNST circuitry to be recruited into gating fear and anxiety-like behaviors.


Subject(s)
Citalopram/pharmacology , Conditioning, Classical/physiology , Fear/physiology , Learning/physiology , Receptor, Serotonin, 5-HT2C/physiology , Selective Serotonin Reuptake Inhibitors/pharmacology , Septal Nuclei/physiology , Animals , Behavior, Animal/drug effects , Behavior, Animal/physiology , Citalopram/administration & dosage , Conditioning, Classical/drug effects , Cues , Fear/drug effects , Learning/drug effects , Male , Rats , Rats, Sprague-Dawley , Receptor, Serotonin, 5-HT2C/drug effects , Septal Nuclei/drug effects , Septal Nuclei/metabolism , Serotonin 5-HT2 Receptor Antagonists/administration & dosage , Serotonin 5-HT2 Receptor Antagonists/pharmacology , Selective Serotonin Reuptake Inhibitors/administration & dosage , Up-Regulation
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