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Morphine Potentiates HIV‐1 gp120–Induced Neuronal Apoptosis
Author(s) -
Shuxian Hu,
Wen S. Sheng,
James R. Lokensgard,
Phillip K. Peterson
Publication year - 2005
Publication title -
the journal of infectious diseases
Language(s) - Uncategorized
Resource type - Journals
SCImago Journal Rank - 2.69
H-Index - 252
eISSN - 1537-6613
pISSN - 0022-1899
DOI - 10.1086/427830
Subject(s) - apoptosis , morphine , p38 mitogen activated protein kinases , neurotoxicity , programmed cell death , intracellular , microbiology and biotechnology , opiate , protein kinase a , biology , kinase , pharmacology , signal transduction , cell culture , neuroscience , chemistry , medicine , receptor , biochemistry , toxicity , genetics
To investigate the effect of opiates on human immunodeficiency virus type 1 (HIV-1)-related neuronal apoptosis, primary human fetal neuronal/glial cell cultures were exposed to gp120(IIIB) in the absence and the presence of morphine. Although morphine by itself had little effect on neuronal survival, the combination of morphine (>/=10(-7) mol/L) and gp120(IIIB) (1 nmol/L) significantly increased neuronal apoptosis. The mechanism whereby morphine potentiates gp120(IIIB)-induced neuronal apoptosis appears to involve activation of the p38 mitogen-activated protein kinase intracellular signaling pathway and microglial cells dispersed within the neuronal/glial cell cultures. These results provide additional insight into the molecular basis whereby opiate abuse could promote HIV-1-associated dementia.

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