Abstract
Human immunodeficiency virus 1 (HIV-1) and its associated proteins can have a profound impact on the central nervous system. Co-morbid abuse of opiates, such as morphine and heroin, is often associated with rapid disease progression and greater neurological dysfunction. The mechanisms by which HIV proteins and opiates cause neuronal damage on their own and together are unclear. The emergence of ferritin heavy chain (FHC) as a negative regulator of the chemokine receptor CXCR4, a co-receptor for HIV, may prove to be important in elucidating the interaction between HIV proteins and opiates. This review summarizes our current knowledge of central nervous system damage inflicted by HIV and opiates, as well as the regulation of CXCR4 by opiate-induced changes in FHC protein levels. We propose that HIV proteins and opiates exhibit an additive or synergistic effect on FHC/CXCR4, thereby decreasing neuronal signaling and function.
Publication types
-
Research Support, N.I.H., Extramural
-
Review
MeSH terms
-
AIDS Dementia Complex / metabolism*
-
AIDS Dementia Complex / physiopathology
-
Acquired Immunodeficiency Syndrome / metabolism*
-
Acquired Immunodeficiency Syndrome / physiopathology
-
Analgesics, Opioid / adverse effects
-
Analgesics, Opioid / metabolism*
-
Analgesics, Opioid / pharmacology
-
Disease Progression
-
Female
-
HIV Envelope Protein gp120 / drug effects
-
HIV Envelope Protein gp120 / metabolism
-
HIV-1 / drug effects*
-
Humans
-
Male
-
Neurons / drug effects
-
Neurons / metabolism*
-
Opioid-Related Disorders / metabolism*
-
Opioid-Related Disorders / physiopathology
-
Receptors, CXCR4 / metabolism
-
Signal Transduction / drug effects
-
tat Gene Products, Human Immunodeficiency Virus / drug effects
-
tat Gene Products, Human Immunodeficiency Virus / metabolism
Substances
-
Analgesics, Opioid
-
HIV Envelope Protein gp120
-
Receptors, CXCR4
-
gp120 protein, Human immunodeficiency virus 1
-
tat Gene Products, Human Immunodeficiency Virus