William Christopher Wetsel
Associate Professor in Psychiatry and Behavioral Sciences
Overview
RESEARCH INTERESTS
Last Updated: 27 October 2020
My laboratory uses genetically-modified mice to study the roles that certain genes and gene products play in the presentation of abnormal neuroendocrine, neurological, and psychiatric responses. Traditionally, the identification of neuroendocrine dysfunction has involved biochemical analyses of hormonal responses, those for neurological disorders have relied upon behavioral and postmortem analyses, and those for psychiatric conditions have depended upon phenomenology. The use of genetic technologies has allowed specific genes in selected cells and in neural pathways to be related to certain molecular, biochemical, cellular, physiological, and behavioral dysfunctions. As the Director of the Mouse Behavioral and Neuroendocrine Analysis Core Facility at Duke University (http://sites.duke.edu/mousebehavioralcore/), we have phenotyped many different lines of inbred and mutant mice for my own work as well as for investigators at Duke and at other research institutions. As a consequence, we have helped to develop many different mouse genetic models of neuroendocrine and neuropsychiatric illness. We are working also with academic medicinal chemists and/or certain pharmacological/biotechnological companies to identify novel compounds that will ameliorate abnormal responses in various mutant mouse models. Some of these preclinical studies have formed a basis for clinical trials in humans.
Selected Grants
Stress and Behavior in Health and Disease awarded by National Institutes of Health (Mentor). 1989 to 2011
Pharmacometabolomics Research Network awarded by National Institutes of Health (Co Investigator). 2010 to 2011
Roles of SAPAP Proteins in Synaptic Function and Compulsive-like Behavior awarded by National Institutes of Health (Co Investigator). 2007 to 2010
Cocaine Withdrawal: A Window of Treatment Opportunity awarded by National Institutes of Health (Co Investigator). 1999 to 2010
Collaborative & Physiological Experiments to Breed CPE KO Mice awarded by National Institutes of Health (Principal Investigator). 2006 to 2007
The Pathophysiology of CMT2A in Cell and Animal Models awarded by National Institutes of Health (Co Investigator). 2006 to 2007
Collaborative & Physiological Experiments to Breed CPE KO Mice awarded by National Institutes of Health (Principal Investigator). 2005
Collaborative & Physiological Experiments awarded by National Institutes of Health (Principal Investigator). 2004 to 2005
Genetic Rescue Of Pro-Lhrh Processing In Cpefat Mice awarded by National Institutes of Health (Principal Investigator). 1998 to 2004
Collaborative & Physiological Experiments of CPE K/O Mice awarded by National Institutes of Health (Principal Investigator). 2002 to 2003
Pages
Weitzel, Douglas H., et al. “Radioprotection of the brain white matter by Mn(III) n-Butoxyethylpyridylporphyrin-based superoxide dismutase mimic MnTnBuOE-2-PyP5+.” Mol Cancer Ther, vol. 14, no. 1, Jan. 2015, pp. 70–79. Pubmed, doi:10.1158/1535-7163.MCT-14-0343. Full Text
Hunanyan, Arsen S., et al. “Knock-in mouse model of alternating hemiplegia of childhood: behavioral and electrophysiologic characterization.” Epilepsia, vol. 56, no. 1, Jan. 2015, pp. 82–93. Pubmed, doi:10.1111/epi.12878. Full Text
Wang, Liangli, et al. “Neuron-specific Sumo1-3 knockdown in mice impairs episodic and fear memories.” Journal of Psychiatry & Neuroscience : Jpn, vol. 39, no. 4, July 2014, pp. 259–66. Epmc, doi:10.1503/jpn.130148. Full Text
Gaier, E. D., et al. “In vivo and in vitro analyses of amygdalar function reveal a role for copper.” J Neurophysiol, vol. 111, no. 10, May 2014, pp. 1927–39. Pubmed, doi:10.1152/jn.00631.2013. Full Text
Deng, Jie V., et al. “MeCP2 phosphorylation limits psychostimulant-induced behavioral and neuronal plasticity.” The Journal of Neuroscience : The Official Journal of the Society for Neuroscience, vol. 34, no. 13, Mar. 2014, pp. 4519–27. Epmc, doi:10.1523/jneurosci.2821-13.2014. Full Text
Sassano, M. F., et al. D2 Functionally Selective Ligands: Novel Therapeutics? Dec. 2013, p. 105. Scopus, doi:10.1016/B978-0-12-800044-1.00091-X. Full Text
Gaier, Eric D., et al. “Peptidylglycine α-amidating monooxygenase heterozygosity alters brain copper handling with region specificity.” J Neurochem, vol. 127, no. 5, Dec. 2013, pp. 605–19. Pubmed, doi:10.1111/jnc.12438. Full Text
Wetsel, William C., et al. “Disruption of the expression of the proprotein convertase PC7 reduces BDNF production and affects learning and memory in mice.” Proc Natl Acad Sci U S A, vol. 110, no. 43, Oct. 2013, pp. 17362–67. Pubmed, doi:10.1073/pnas.1314698110. Full Text
Gomes, Ivone, et al. “GPR171 is a hypothalamic G protein-coupled receptor for BigLEN, a neuropeptide involved in feeding.” Proc Natl Acad Sci U S A, vol. 110, no. 40, Oct. 2013, pp. 16211–16. Pubmed, doi:10.1073/pnas.1312938110. Full Text
Sachs, Benjamin D., et al. “The effects of brain serotonin deficiency on behavioural disinhibition and anxiety-like behaviour following mild early life stress.” The International Journal of Neuropsychopharmacology, vol. 16, no. 9, Oct. 2013, pp. 2081–94. Epmc, doi:10.1017/s1461145713000321. Full Text