Revision: Drug dependence is linked to diminished hippocampal structure and function, and the hippocampus is involved in drug reward and relapse to drug seeking. Thus, our understanding and treatment of addiction will be greatly improved if we can clarify the time course, extent, and cause of drug-induced hippocampal neuroadaptations and identify if and how hippocampal neuroadaptations impact addictive behaviors. A notable aspect of the hippocampus is its ability to generate new neurons throughout life. Adult-generated neurons are functionally integrated into hippocampal circuitry and are involved in some types of learning. Drugs of abuse, like morphine, decrease neurogenesis in the hippocampal dentate gyrus subgranular zone (SGZ), raising the possibility that opiate-induced alteration in neurogenesis leads to cognitive deficits, continued drug taking or relapse, or otherwise impedes recovery. The parent grant application, DA 016765, has three aims to test this possibility:
Aim 1) Determine how morphine self-administration and withdrawal alter discrete stages of adult hippocampal neurogenesis.
Aim 2) Assess how altered adult hippocampal neurogenesis relates to drug seeking.
Aim 3) Evaluate the involvement of adult-generated hippocampal neurons in drug/context association. For this competitive revision, we propose a new aim to be completed in one year:
Aim 4) Evaluate the involvement of adult-generated hippocampal neurogenesis in the vulnerability to morphine addiction. Based on our recent publication (Noonan et al., J Neuroscience, 2010), we hypothesize that ablation of adult neurogenesis via cranial radiation will enhance vulnerability to self-administration in an animal model of opiate addiction without disrupting response to non-drug rewards. The extensive analysis of behavior in this new aim will reveal how adult-generated neurons contribute to basal and reward-based behavior, and makes this aim perfectly-suited for consideration through the NIH Basic Behavioral and Social Sciences Opportunity Network. By providing insight into the relationship among adult neurogenesis, opiates, and behavior, these studies will provide much-needed information relevant to our understanding of the addicted and the non-addicted brain and may indicate novel avenues to treat and prevent addiction and improve brain health in general.

Public Health Relevance

Drug addiction is a devastating disorder marked by compulsive drug use, high propensity to relapse to drug taking, and cognitive deficits. Drugs of abuse, including morphine, lead to a decrease in the number of new neurons in the hippocampus, a brain region important for learning and memory. We will explore the potentially reciprocal relationship between opiate addiction and adult hippocampal neurogenesis, thus providing much- needed insight into the structure and function of the addicted brain as well as the function of adult-generated neurons in the non-addicted brain.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
3R01DA016765-07S1
Application #
8038861
Study Section
Special Emphasis Panel (ZRG1-IFCN-C (85))
Program Officer
Pilotte, Nancy S
Project Start
2003-07-01
Project End
2012-09-29
Budget Start
2010-09-30
Budget End
2012-09-29
Support Year
7
Fiscal Year
2010
Total Cost
$237,750
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Psychiatry
Type
Schools of Medicine
DUNS #
800771545
City
Dallas
State
TX
Country
United States
Zip Code
75390
Bulin, Sarah E; Mendoza, Matthew L; Richardson, Devon R et al. (2018) Dentate gyrus neurogenesis ablation via cranial irradiation enhances morphine self-administration and locomotor sensitization. Addict Biol 23:665-675
Whoolery, Cody W; Walker, Angela K; Richardson, Devon R et al. (2017) Whole-Body Exposure to 28Si-Radiation Dose-Dependently Disrupts Dentate Gyrus Neurogenesis and Proliferation in the Short Term and New Neuron Survival and Contextual Fear Conditioning in the Long Term. Radiat Res 188:532-551
Yun, Sanghee; Donovan, Michael H; Ross, Michele N et al. (2016) Stress-Induced Anxiety- and Depressive-Like Phenotype Associated with Transient Reduction in Neurogenesis in Adult Nestin-CreERT2/Diphtheria Toxin Fragment A Transgenic Mice. PLoS One 11:e0147256
Petrik, David; Latchney, Sarah E; Masiulis, Irene et al. (2015) Chromatin Remodeling Factor Brg1 Supports the Early Maintenance and Late Responsiveness of Nestin-Lineage Adult Neural Stem and Progenitor Cells. Stem Cells 33:3655-65
Cho, Kyung-Ok; Lybrand, Zane R; Ito, Naoki et al. (2015) Aberrant hippocampal neurogenesis contributes to epilepsy and associated cognitive decline. Nat Commun 6:6606
Latchney, Sarah E; Jaramillo, Thomas C; Rivera, Phillip D et al. (2015) Chronic P7C3 treatment restores hippocampal neurogenesis in the Ts65Dn mouse model of Down Syndrome [Corrected]. Neurosci Lett 591:86-92
Latchney, Sarah E; Jiang, Yindi; Petrik, David P et al. (2015) Inducible knockout of Mef2a, -c, and -d from nestin-expressing stem/progenitor cells and their progeny unexpectedly uncouples neurogenesis and dendritogenesis in vivo. FASEB J 29:5059-71
Rivera, Phillip D; Raghavan, Ramya K; Yun, Sanghee et al. (2015) Retrieval of morphine-associated context induces cFos in dentate gyrus neurons. Hippocampus 25:409-14
Walker, A K; Rivera, P D; Wang, Q et al. (2015) The P7C3 class of neuroprotective compounds exerts antidepressant efficacy in mice by increasing hippocampal neurogenesis. Mol Psychiatry 20:500-8
DeCarolis, Nathan A; Rivera, Phillip D; Ahn, Francisca et al. (2014) 56 Fe Particle Exposure Results in a Long-Lasting Increase in a Cellular Index of Genomic Instability and Transiently Suppresses Adult Hippocampal Neurogenesisin Vivo. Life Sci Space Res (Amst) 2:70-79

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