Women now constitute one of the fastest growing populations becoming infected with HIV. Drug use plays a major role in the spread of this disease in women and drug abusers are more likely to have neurological complications with HIV infection. In the prior funding period, potential neural mechanisms and target sites for cocaine-HIV interactions in the female brain were identified, leading to the following questions: Are dopaminergic neurochemical systems a preferential target for cocaine+HIV-induced neurotoxicity? And moreover, is the dopamine transporter protein (DAT) a primary target for this cocaine-viral interaction? Recent studies have shown that DAT is reduced in patients with HIV and cognitive deficits, but the mechanisms for this reduction are unknown and current therapeutic strategies unsuccessful. However, dopaminergic systems are known to be responsive to estrogens, and estrogens may provide a unique therapeutic opportunity in women for treatment of HIV-associated cognitive and motor dysfunction. First, the effects of cellular oxidative stress produced by cocaine+Tat/gp120 on monoamine transporters (DAT, NET and SERT) will be determined. We have found that oxidative stress plays an important role in cocaine+Tat/gp120 neurotoxicity and the ability of estrogenic compounds to prevent this stress will be assessed. Second, we will test the ability of estrogen to modulate dopaminergic markers under physiological conditions in female rats exposed to cocaine+Tat/gp120. The function of DAT will be determined using in vivo microdialysis. Third, we will determine whether cocaine+Tat/gp120 produces dopaminergic dysfunction by altering intracellular regulation of DAT signaling mechanisms. Estrogens will be used to modulate intracellular proteins following cocaine+Tat neurotoxicity, providing insight into potential key mechanisms and for developing novel therapeutic strategies. Our gender-based orientation, in combination with HIV protein neurotoxicity, is innovative and will be translational to the important women's health issues of drug abuse and the neurological complications of AIDS. The ultimate goal of this research is to identify the critical neurological targets of HIV infection and to develop innovative pharmacological strategies for preventing cognitive and motor dysfunction following HIV infection in drug abusing women.

Agency
National Institute of Health (NIH)
Institute
National Institute on Drug Abuse (NIDA)
Type
Research Project (R01)
Project #
3R01DA013137-07S1
Application #
7275831
Study Section
NeuroAIDS and other End-Organ Diseases Study Section (NAED)
Program Officer
Lawrence, Diane M
Project Start
1999-09-01
Project End
2010-08-31
Budget Start
2006-09-01
Budget End
2007-08-31
Support Year
7
Fiscal Year
2006
Total Cost
$40,178
Indirect Cost
Name
University of South Carolina at Columbia
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
041387846
City
Columbia
State
SC
Country
United States
Zip Code
29208
Li, Hailong; Illenberger, Jessica M; McLaurin, Kristen A et al. (2018) Identification of Dopamine D1-Alpha Receptor Within Rodent Nucleus Accumbens by an Innovative RNA In Situ Detection Technology. J Vis Exp :
McLaurin, Kristen A; Booze, Rosemarie M; Mactutus, Charles F (2018) Evolution of the HIV-1 transgenic rat: utility in assessing the progression of HIV-1-associated neurocognitive disorders. J Neurovirol 24:229-245
Bertrand, Sarah J; Mactutus, Charles F; Harrod, Steven B et al. (2018) HIV-1 proteins dysregulate motivational processes and dopamine circuitry. Sci Rep 8:7869
Mohseni Ahooyi, Taha; Shekarabi, Masoud; Torkzaban, Bahareh et al. (2018) Dysregulation of Neuronal Cholesterol Homeostasis upon Exposure to HIV-1 Tat and Cocaine Revealed by RNA-Sequencing. Sci Rep 8:16300
Fitting, Sylvia; McLaurin, Kristen A; Booze, Rosemarie M et al. (2018) Dose-dependent neurocognitive deficits following postnatal day 10 HIV-1 viral protein exposure: Relationship to hippocampal anatomy parameters. Int J Dev Neurosci 65:66-82
McLaurin, Kristen A; Li, Hailong; Booze, Rosemarie M et al. (2018) Unraveling Individual Differences In The HIV-1 Transgenic Rat: Therapeutic Efficacy Of Methylphenidate. Sci Rep 8:136
McLaurin, Kristen A; Moran, Landhing M; Li, Hailong et al. (2017) A Gap in Time: Extending our Knowledge of Temporal Processing Deficits in the HIV-1 Transgenic Rat. J Neuroimmune Pharmacol 12:171-179
McLaurin, Kristen A; Booze, Rosemarie M; Mactutus, Charles F (2017) Selective developmental alterations in The HIV-1 transgenic rat: Opportunities for diagnosis of pediatric HIV-1. J Neurovirol 23:87-98
McLaurin, Kristen A; Booze, Rosemarie M; Mactutus, Charles F et al. (2017) Sex Matters: Robust Sex Differences in Signal Detection in the HIV-1 Transgenic Rat. Front Behav Neurosci 11:212
Javadi-Paydar, Mehrak; Roscoe Jr, Robert F; Denton, Adam R et al. (2017) HIV-1 and cocaine disrupt dopamine reuptake and medium spiny neurons in female rat striatum. PLoS One 12:e0188404

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