Neurotrophic factors are best characterized for their role in nervous system development and differentiation, although more recently they have been implicated in the regulation of neural plasticity in adult animals. The major objective of the application is to study such a role for neurotrophic factors in the neural plasticity that accompanies chronic exposure to drugs of abuse. This competing renewal focuses on interactions between two neurotrophic factors, BDNF and GDNF, and the actions of two drugs of abuse, morphine and cocaine, at the level of the mesolimbic dopamine system, a neural pathway important for the reinforcing actions of these and other drugs of abuse. Work over the first five years of this application supports three major types of interactions between neurotrophic factors and drugs of abuse, with interesting differences and similarities exerted by BDNF versus GDNF. First, we have shown that exogenous neurotrophic factors can modify the ability of drugs of abuse to produce certain characteristic biochemical adaptations in the mesolimbic dopamine system. Exogenous neurotrophic factors also modify the rewarding and locomotor-activating effects of these drugs. Second we have demonstrated that chronic exposure to morphine or cocaine causes alterations in specific neurotrophic factor signaling proteins, and in preliminary studies, show that such alterations may contribute to the behavioral effects of these drugs. Third, by use of mutant mice and other approaches, we have provided evidence that endogenous neurotrophic factor pathways are involved in controlling an animal's responsiveness to drug exposure. The goal of the proposed studies is to further characterize these interactions and to begin the process of relating specific molecular phenomena to behavioral responses to drugs of abuse, by use of viral-mediated gene transfer and genetic mutations in mice. These proposed studies will improve our understanding of the role played by neurotrophic factors in regulating an animal's responsiveness to drugs of abuse. Moreover, in a general sense, the studies will utilize models of addiction to better understand the continued influence of neurotrophic factors in controlling mesolimbic dopamine function in the fully differentiated, adult brain.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
5R01DA014133-02
Application #
6379146
Study Section
Special Emphasis Panel (ZRG1-MDCN-5 (01))
Program Officer
Pilotte, Nancy S
Project Start
2000-09-01
Project End
2005-06-30
Budget Start
2001-07-01
Budget End
2002-06-30
Support Year
2
Fiscal Year
2001
Total Cost
$312,000
Indirect Cost
Name
University of Texas Sw Medical Center Dallas
Department
Psychiatry
Type
Schools of Medicine
DUNS #
City
Dallas
State
TX
Country
United States
Zip Code
75390
Cahill, Michael E; Browne, Caleb J; Wang, Junshi et al. (2018) Withdrawal from repeated morphine administration augments expression of the RhoA network in the nucleus accumbens to control synaptic structure. J Neurochem 147:84-98
Mul, Joram D; Soto, Marion; Cahill, Michael E et al. (2018) Voluntary wheel running promotes resilience to chronic social defeat stress in mice: a role for nucleus accumbens ?FosB. Neuropsychopharmacology 43:1934-1942
Ribeiro, Efrain A; Salery, Marine; Scarpa, Joseph R et al. (2018) Transcriptional and physiological adaptations in nucleus accumbens somatostatin interneurons that regulate behavioral responses to cocaine. Nat Commun 9:3149
Cahill, M E; Walker, D M; Gancarz, A M et al. (2018) The dendritic spine morphogenic effects of repeated cocaine use occur through the regulation of serum response factor signaling. Mol Psychiatry 23:1474-1486
Muir, Jessie; Lorsch, Zachary S; Ramakrishnan, Charu et al. (2018) In Vivo Fiber Photometry Reveals Signature of Future Stress Susceptibility in Nucleus Accumbens. Neuropsychopharmacology 43:255-263
Calipari, Erin S; Godino, Arthur; Peck, Emily G et al. (2018) Granulocyte-colony stimulating factor controls neural and behavioral plasticity in response to cocaine. Nat Commun 9:9
Yu, Jun; Yan, Yijin; Li, King-Lun et al. (2017) Nucleus accumbens feedforward inhibition circuit promotes cocaine self-administration. Proc Natl Acad Sci U S A 114:E8750-E8759
Anderson, Ethan M; Wissman, Anne Marie; Chemplanikal, Joyce et al. (2017) BDNF-TrkB controls cocaine-induced dendritic spines in rodent nucleus accumbens dissociated from increases in addictive behaviors. Proc Natl Acad Sci U S A 114:9469-9474
Ceglia, Ilaria; Lee, Ko-Woon; Cahill, Michael E et al. (2017) WAVE1 in neurons expressing the D1 dopamine receptor regulates cellular and behavioral actions of cocaine. Proc Natl Acad Sci U S A 114:1395-1400
Calipari, Erin S; Juarez, Barbara; Morel, Carole et al. (2017) Dopaminergic dynamics underlying sex-specific cocaine reward. Nat Commun 8:13877

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