Vasopressin (AVP) is a peptide produced in the brain and released both centrally and peripherally. The central actions of AVP include effects on both social and non-social behaviors. Two main subtypes of AVP receptors exist in the brain, namely V1alpha and V1beta. It is unclear via which receptor subtype AVP acts to affect these behaviors. Understanding the mechanisms behind AVP's effects on anxiety and social recognition is particularly important given the relationship between these behaviors and human disorders such as anxiety disorder and autism.
The aims of this proposal are to use mice with a null mutation in the V1alpha receptor (V1aRKO) to better understand how AVP affects anxiety and social behavior. In the first aim, the V1aRKO mice will be behaviorally and neurochemically phenotyped to assess the effects of a null mutation in the V1aR. In the second aim, differences in c-fos-IR between the V1aRKOs and WT animals will be used to determine neuroanatomical regions involved in anxiety and social behavior. In the third aim, a V1aR viral vector will be used to re-express the V1aR in specific neuroanatomical regions, in an attempt to alter the anxiety and social behavior of the KO mice. These experiments will further our understanding of the mechanisms involved in AVP mediated anxiety and social behavior. ? ?

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Predoctoral Individual National Research Service Award (F31)
Project #
5F31MH070112-02
Application #
6805655
Study Section
Special Emphasis Panel (ZRG1-F02A (20))
Program Officer
Curvey, Mary F
Project Start
2003-09-16
Project End
2005-05-16
Budget Start
2004-09-16
Budget End
2005-05-16
Support Year
2
Fiscal Year
2004
Total Cost
$18,356
Indirect Cost
Name
Emory University
Department
Psychiatry
Type
Schools of Medicine
DUNS #
066469933
City
Atlanta
State
GA
Country
United States
Zip Code
30322
Bielsky, Isadora F; Hu, Shuang-Bao; Ren, Xianghui et al. (2005) The V1a vasopressin receptor is necessary and sufficient for normal social recognition: a gene replacement study. Neuron 47:503-13
Bielsky, Isadora F; Hu, Shuang-Bao; Young, Larry J (2005) Sexual dimorphism in the vasopressin system: lack of an altered behavioral phenotype in female V1a receptor knockout mice. Behav Brain Res 164:132-6
Lim, Miranda M; Bielsky, Isadora F; Young, Larry J (2005) Neuropeptides and the social brain: potential rodent models of autism. Int J Dev Neurosci 23:235-43
Bielsky, Isadora F; Young, Larry J (2004) Oxytocin, vasopressin, and social recognition in mammals. Peptides 25:1565-74