Literature DB >> 22801411

Neuropeptide Y and posttraumatic stress disorder.

R Sah1, T D Geracioti.   

Abstract

Resiliency to the adverse effects of extraordinary emotional trauma on the brain varies within the human population. Accordingly, some people cope better than others with traumatic stress. Neuropeptide Y (NPY) is a 36-amino-acid peptide transmitter abundantly expressed in forebrain limbic and brain stem areas that regulate stress and emotional behaviors. Studies largely in rodents demonstrate a role for NPY in promoting coping with stress. Moreover, accruing data from the genetic to the physiological implicate NPY as a potential 'resilience-to-stress' factor in humans. Here, we consolidate findings from preclinical and clinical studies of NPY that are of relevance to stress-associated syndromes, most prototypically posttraumatic stress disorder (PTSD). Collectively, these data suggest that reduced central nervous system (CNS) NPY concentrations or function may be associated with PTSD. We also link specific symptoms of human PTSD with extant findings in the NPY field to reveal potential physiological contributions of the neuropeptide to the disorder. In pursuit of understanding the physiological basis and treatment of PTSD, the NPY system is an attractive target.

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Year:  2012        PMID: 22801411      PMCID: PMC4749915          DOI: 10.1038/mp.2012.101

Source DB:  PubMed          Journal:  Mol Psychiatry        ISSN: 1359-4184            Impact factor:   15.992


  159 in total

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10.  Effect of a graded single constriction of the rat sciatic nerve on pain behavior and expression of immunoreactive NPY and NPY Y1 receptor in DRG neurons and spinal cord.

Authors:  P R Brumovsky; E Bergman; H-X Liu; T Hökfelt; M J Villar
Journal:  Brain Res       Date:  2004-04-23       Impact factor: 3.252

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8.  Effects of varying intensities of heat stress on neuropeptide Y and proopiomelanocortin mRNA expression in rats.

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Review 9.  The Genetics of Stress-Related Disorders: PTSD, Depression, and Anxiety Disorders.

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10.  NPY Y1 receptors differentially modulate GABAA and NMDA receptors via divergent signal-transduction pathways to reduce excitability of amygdala neurons.

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