This is a proposal for a regional training grant to support ten predoctoral and five postdoctoral trainees who will be broadly and intensively trained to conduct interdisciplinary research in behavioral neuroscience. The goal is to increase the number of behavioral neuroscientists from underrepresented populations who will be trained to undertake high quality research relevant to the missions of NIMH, NIDA and NINDS. The program direction benefits from Hispanic and African American leaders with demonstrated knowledge of successful Neuroscience training programs for minorities. The faculty comprises 24 NIH-funded PI?s selected from a consortium of five Texas universities: University of Texas at Austin, University of Texas at San Antonio, University of Texas Health Science Center at San Antonio, Texas A&M University, and Texas A&M University System Health Science Center. These institutions were selected to complement their strengths to achieve the program goal. The training faculty already collaborates in behavioral neuroscience research, participates in active pre- and postdoctoral neuroscience programs, and is committed to increasing diversity .The program plan is based on the broad experience of the faculty with underrepresented predoctoral and postdoctoral students as part of both national and institutional NIH-funded training programs. The proposed training will span the breadth of state-of-the-art approaches to behavioral brain research, including brain metabolic mapping of behavioral functions, neuropharmacology, electrophysiology and molecular neurobiology. Predoctoral trainees will be required to complete courses covering the brain and behavior, scientific ethics, experimental design and statistical analysis. Postdoctoral trainees will choose a project at the onset of their training. The training will emphasize professional development, including improvement of oral and written communication skills. The program proposes national and regional strategies to recruit predoctoral and postdoctoral minority students, and seeks to increase their success by providing successful minority faculty as role models, by offering proper support and enrichment activities, and by creating a responsive mentor-based learning environment for incoming students. Major strengths of this program are: 1) the breadth and relevant experience of the faculty and advisory committee, 2) the favorable ratio of trainees to preceptors, 3) the enrichment and networking opportunities beyond those provided by the individual institutions, 4) the close research and intellectual interaction among all participants, and 5) the size and manageability of the program.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Institutional National Research Service Award (T32)
Project #
1T32MH065728-01
Application #
6486416
Study Section
Special Emphasis Panel (ZMH1-BRB-S (01))
Program Officer
Desmond, Nancy L
Project Start
2002-07-01
Project End
2007-06-30
Budget Start
2002-07-01
Budget End
2003-06-30
Support Year
1
Fiscal Year
2002
Total Cost
$563,837
Indirect Cost
Name
University of Texas Austin
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
City
Austin
State
TX
Country
United States
Zip Code
78712
Damborsky, Joanne C; Griffith, William H; Winzer-Serhan, Ursula H (2015) Neonatal nicotine exposure increases excitatory synaptic transmission and attenuates nicotine-stimulated GABA release in the adult rat hippocampus. Neuropharmacology 88:187-98
Bastida, Christel C; Puga, Frank; Gonzalez-Lima, Francisco et al. (2014) Chronic social stress in puberty alters appetitive male sexual behavior and neural metabolic activity. Horm Behav 66:220-7
Trujillo, Logan T; Jankowitsch, Jessica M; Langlois, Judith H (2014) Beauty is in the ease of the beholding: a neurophysiological test of the averageness theory of facial attractiveness. Cogn Affect Behav Neurosci 14:1061-76
Vélez-Hernández, M E; Padilla, E; Gonzalez-Lima, F et al. (2014) Cocaine reduces cytochrome oxidase activity in the prefrontal cortex and modifies its functional connectivity with brainstem nuclei. Brain Res 1542:56-69
Velez-Hernandez, M E; Padilla, E; Gonzalez-Lima, F et al. (2013) Cocaine reduces cytochrome oxidase activity in the prefrontal cortex and modifies its functional connectivity with brainstem nuclei. Brain Res :
Mendez, I A; Damborsky, J C; Winzer-Serhan, U H et al. (2013) ýý4ýý2 and ýý7 nicotinic acetylcholine receptor binding predicts choice preference in two cost benefit decision-making tasks. Neuroscience 230:121-31
Damborsky, J C; Winzer-Serhan, U H (2012) Effects of sex and chronic neonatal nicotine treatment on Naýýýýý/Kýýý/Clýýý co-transporter 1, Kýýý/Clýýý co-transporter 2, brain-derived neurotrophic factor, NMDA receptor subunit 2A and NMDA receptor subunit 2B mRNA expression in the postnatal rat hippo Neuroscience 225:105-17
Rojas, Julio C; Bruchey, Aleksandra K; Gonzalez-Lima, Francisco (2012) Low-level light therapy improves cortical metabolic capacity and memory retention. J Alzheimers Dis 32:741-52
Mendez, Ian A; Gilbert, Ryan J; Bizon, Jennifer L et al. (2012) Effects of acute administration of nicotinic and muscarinic cholinergic agonists and antagonists on performance in different cost-benefit decision making tasks in rats. Psychopharmacology (Berl) 224:489-99
Damborsky, Joanne C; Griffith, William H; Winzer-Serhan, Ursula H (2012) Chronic neonatal nicotine exposure increases excitation in the young adult rat hippocampus in a sex-dependent manner. Brain Res 1430:8-17

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