NPY controls fear conditioning and fear extinction by combined action on Y1 and Y2 receptors

• Published in: British journal of pharmacology Vol. 166; no. 4; pp. 1461 - 1473
• Main Authors: Verma, D, Tasan, RO, Herzog, H, Sperk, G
• Format: Journal Article
• Language: English
• Published: Oxford, UK Blackwell Publishing Ltd 01.06.2012; Nature Publishing Group
• Subjects: Acquisitions & mergers; Animals; Anxiety Disorders - metabolism; Behavior, Animal; Biological and medical sciences; Conditioning, Classical; Discrimination, Psychological; Extinction, Psychological; Fear; fear conditioning; fear extinction; Male; Medical research; Medical sciences; Mice; Mice, 129 Strain; Mice, Inbred C57BL; Mice, Knockout; neuropeptide Y; Neuropeptide Y - genetics; Neuropeptide Y - metabolism; NPY; Pharmacology. Drug treatments; Receptors, Neuropeptide Y - genetics; Receptors, Neuropeptide Y - metabolism; Research Papers; Rodents; Signal Transduction; Y1 receptor; Y2 receptor; Neuropeptide Y; Fear; receptor; fear conditioning; NPY; fear extinction; Peptide hormone; Y; Conditioning; Biological receptor
• ISSN: 0007-1188; 1476-5381
• DOI: 10.1111/j.1476-5381.2012.01872.x

BACKGROUND AND PURPOSE Neuropeptide Y (NPY) and its receptors have been implicated in the control of emotional‐affective processing, but the mechanism is unclear. While it is increasingly evident that stimulation of Y1 and inhibition of Y2 receptors produce prominent anxiolytic and antidepressant effects, the contribution of the individual NPY receptor subtypes in the acquisition and extinction of learned fear are unknown. EXPERIMENTAL APPROACH Here we performed Pavlovian fear conditioning and extinction in NPY knockout (KO) and in NPY receptor KO mice. KEY RESULTS NPY KO mice display a dramatically accelerated acquisition of conditioned fear. Deletion of Y1 receptors revealed only a moderately accelerated acquisition of conditioned fear, while lack of Y2 receptors was without any effect on fear learning. However, the strong phenotype seen in NPY KO mice was reproduced in mice lacking both Y1 and Y2 receptors. In addition, NPY KO mice showed excessive recall of conditioned fear and impaired fear extinction. This behaviour was replicated only after deletion of both Y1 and Y2 receptors. In Y1 receptor single KO mice, fear extinction was delayed and was unchanged in Y2 receptor KO mice. Deletion of NPY and particularly Y2 receptors resulted in a generalization of conditioned fear. CONCLUSIONS AND IMPLICATIONS Our data demonstrate that NPY delays the acquisition, reduces the expression of conditioned fear while promoting fear extinction. Although these effects appear to be primarily mediated by Y1 receptors, the pronounced phenotype of Y1Y2 receptor double KO mice suggests a synergistic role of Y2 receptors in fear acquisition and in fear extinction.