HIV, Tat and dopamine transmission

Human Immunodeficiency Virus (HIV) is a progressive infection that targets the immune system, affecting more than 37 million people around the world. While combinatorial antiretroviral therapy (cART) has lowered mortality rates and improved quality of life in infected individuals, the prevalence of...

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Main Authors: Peter J. Gaskill, Douglas R. Miller, Joyonna Gamble-George, Hideaki Yano, Habibeh Khoshbouei
Format: Article
Language:English
Published: Elsevier 2017-09-01
Series:Neurobiology of Disease
Subjects:
HIV
Tat
Online Access:http://www.sciencedirect.com/science/article/pii/S096999611730089X
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spelling doaj-91c1cd0649d2487196c273b7928811812021-03-22T12:45:25ZengElsevierNeurobiology of Disease1095-953X2017-09-011055173HIV, Tat and dopamine transmissionPeter J. Gaskill0Douglas R. Miller1Joyonna Gamble-George2Hideaki Yano3Habibeh Khoshbouei4Department of Pharmacology and Physiology, Drexel University College of Medicine, Philadelphia, PA 19102, United States; Correspondence to: P. Gaskill, Department of Pharmacology and Physiology, Drexel University College of Medicine, United States.Department of Neuroscience, University of Florida, Gainesville, FL 32611, United StatesDepartment of Neuroscience, University of Florida, Gainesville, FL 32611, United StatesNational Institute on Drug Abuse, National Institutes of Health, Baltimore, MD 21224, United StatesDepartment of Neuroscience, University of Florida, Gainesville, FL 32611, United States; Correspondence to: H. Khoshbouei, Department of Neuroscience, University of Florida, United States.Human Immunodeficiency Virus (HIV) is a progressive infection that targets the immune system, affecting more than 37 million people around the world. While combinatorial antiretroviral therapy (cART) has lowered mortality rates and improved quality of life in infected individuals, the prevalence of HIV associated neurocognitive disorders is increasing and HIV associated cognitive decline remains prevalent. Recent research has suggested that HIV accessory proteins may be involved in this decline, and several studies have indicated that the HIV protein transactivator of transcription (Tat) can disrupt normal neuronal and glial function. Specifically, data indicate that Tat may directly impact dopaminergic neurotransmission, by modulating the function of the dopamine transporter and specifically damaging dopamine-rich regions of the CNS. HIV infection of the CNS has long been associated with dopaminergic dysfunction, but the mechanisms remain undefined. The specific effect(s) of Tat on dopaminergic neurotransmission may be, at least partially, a mechanism by which HIV infection directly or indirectly induces dopaminergic dysfunction. Therefore, precisely defining the specific effects of Tat on the dopaminergic system will help to elucidate the mechanisms by which HIV infection of the CNS induces neuropsychiatric, neurocognitive and neurological disorders that involve dopaminergic neurotransmission. Further, this will provide a discussion of the experiments needed to further these investigations, and may help to identify or develop new therapeutic approaches for the prevention or treatment of these disorders in HIV-infected individuals.http://www.sciencedirect.com/science/article/pii/S096999611730089XDopamineHIVTatHIV-associated neurocognitive disordersneurological diseaseneurotransmission
collection DOAJ
language English
format Article
sources DOAJ
author Peter J. Gaskill
Douglas R. Miller
Joyonna Gamble-George
Hideaki Yano
Habibeh Khoshbouei
spellingShingle Peter J. Gaskill
Douglas R. Miller
Joyonna Gamble-George
Hideaki Yano
Habibeh Khoshbouei
HIV, Tat and dopamine transmission
Neurobiology of Disease
Dopamine
HIV
Tat
HIV-associated neurocognitive disorders
neurological disease
neurotransmission
author_facet Peter J. Gaskill
Douglas R. Miller
Joyonna Gamble-George
Hideaki Yano
Habibeh Khoshbouei
author_sort Peter J. Gaskill
title HIV, Tat and dopamine transmission
title_short HIV, Tat and dopamine transmission
title_full HIV, Tat and dopamine transmission
title_fullStr HIV, Tat and dopamine transmission
title_full_unstemmed HIV, Tat and dopamine transmission
title_sort hiv, tat and dopamine transmission
publisher Elsevier
series Neurobiology of Disease
issn 1095-953X
publishDate 2017-09-01
description Human Immunodeficiency Virus (HIV) is a progressive infection that targets the immune system, affecting more than 37 million people around the world. While combinatorial antiretroviral therapy (cART) has lowered mortality rates and improved quality of life in infected individuals, the prevalence of HIV associated neurocognitive disorders is increasing and HIV associated cognitive decline remains prevalent. Recent research has suggested that HIV accessory proteins may be involved in this decline, and several studies have indicated that the HIV protein transactivator of transcription (Tat) can disrupt normal neuronal and glial function. Specifically, data indicate that Tat may directly impact dopaminergic neurotransmission, by modulating the function of the dopamine transporter and specifically damaging dopamine-rich regions of the CNS. HIV infection of the CNS has long been associated with dopaminergic dysfunction, but the mechanisms remain undefined. The specific effect(s) of Tat on dopaminergic neurotransmission may be, at least partially, a mechanism by which HIV infection directly or indirectly induces dopaminergic dysfunction. Therefore, precisely defining the specific effects of Tat on the dopaminergic system will help to elucidate the mechanisms by which HIV infection of the CNS induces neuropsychiatric, neurocognitive and neurological disorders that involve dopaminergic neurotransmission. Further, this will provide a discussion of the experiments needed to further these investigations, and may help to identify or develop new therapeutic approaches for the prevention or treatment of these disorders in HIV-infected individuals.
topic Dopamine
HIV
Tat
HIV-associated neurocognitive disorders
neurological disease
neurotransmission
url http://www.sciencedirect.com/science/article/pii/S096999611730089X
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