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The Effects of Prior Stress on Anxiety-Like Responding to Intra-BNST Pituitary Adenylate Cyclase Activating Polypeptide in Male and Female Rats
Journal article   Open access   Peer reviewed

The Effects of Prior Stress on Anxiety-Like Responding to Intra-BNST Pituitary Adenylate Cyclase Activating Polypeptide in Male and Female Rats

S Bradley King, Kim R Lezak, Micaela O'Reilly, Donna J Toufexis, William A Falls, Karen Braas, Victor May and Sayamwong E Hammack
Neuropsychopharmacology (New York, N.Y.), v 42(8), pp 1679-1687
Jul 2017
PMID: 28106040
url
https://www.nature.com/articles/npp201716.pdfView
Published, Version of Record (VoR) Open
url
https://doi.org/10.1038/npp.2017.16View
Published, Version of Record (VoR) Open

Abstract

Animals Anxiety - physiopathology Corticosterone - blood Female Male Microinjections Pituitary Adenylate Cyclase-Activating Polypeptide - administration & dosage Pituitary Adenylate Cyclase-Activating Polypeptide - pharmacology Pituitary Adenylate Cyclase-Activating Polypeptide - physiology Rats Reflex, Startle - drug effects Septal Nuclei - drug effects Septal Nuclei - physiology Sex Characteristics Stress, Psychological - physiopathology Vasoactive Intestinal Peptide - administration & dosage Vasoactive Intestinal Peptide - pharmacology
Chronic or repeated exposure to stressful stimuli can result in several maladaptive consequences, including increased anxiety-like behaviors and altered peptide expression in anxiety-related brain structures. Among these structures, the bed nucleus of the stria terminalis (BNST) has been implicated in emotional behaviors as well as regulation of hypothalamic-pituitary-adrenal (HPA) axis activity. In male rodents, chronic variate stress (CVS) has been shown to increase BNST pituitary adenylate cyclase activating polypeptide (PACAP) and its cognate PAC1 receptor transcript, and BNST PACAP signaling may mediate the maladaptive changes associated with chronic stress. Here, we examined whether CVS would sensitize the behavioral and/or endocrine response to a subthreshold BNST PACAP infusion. Male and cycling female rats were exposed to a 7 day CVS paradigm previously shown to upregulate BNST PAC1 receptor transcripts; control rats were not stressed. Twenty-four hours following the last stressor, rats were bilaterally infused into the BNST with a normally subthreshold dose of PACAP. We found an increase in startle amplitude and plasma corticosterone levels 30 min following intra-BNST PACAP infusion in male rats that had been previously exposed to CVS. CVS did not enhance the startle response in cycling females. Equimolar infusion of the VPAC1/2 receptor ligand vasoactive intestinal polypeptide (VIP) had no effect on plasma corticosterone levels even in previously stressed male rats. These results suggest that repeated exposure to stressors may differentially alter the neural circuits underlying the responses to intra-BNST PACAP, and may result in different anxiety-like responses in males and females.

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Collaboration types
Domestic collaboration
Web of Science research areas
Neurosciences
Pharmacology & Pharmacy
Psychiatry
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