Literature DB >> 12498789

Lithium ameliorates HIV-gp120-mediated neurotoxicity.

Ian P Everall1, Christopher Bell, Margaret Mallory, Dianne Langford, Anthony Adame, Edward Rockestein, Eliezer Masliah.   

Abstract

To investigate the protective effects of lithium against HIV-gp120-mediated toxicity in vivo, mice were exposed to lithium and gp120 and levels of the neuronal markers, microtubule-associated protein-2 and NeuN, and the astrocyte marker, glial fibrillary acidic protein, were determined. In addition, SH-SY5Y neuronal cells exposed to gp120 and lithium were assessed for cell viability. Lithium pretreatment protected the hippocampus of mice from gp120-mediated toxicity. Similarly, preexposure of neuronal cultures to lithium significantly reduced gp120-associated neurotoxicity. However, posttreatment with lithium had minimal neuroprotective effects against gp120, both in vivo and in vitro. The protective effects of lithium in vitro were blocked by LY294002, an inhibitor of the phosphatidylinositol 3-kinase/Akt pathway. Taken together, these results demonstrate that lithium might be neuroprotective against gp120-mediated toxicity and suggest that prophylactic treatment with lithium may prevent the onset/progression of HIV-associated cognitive impairments.

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Year:  2002        PMID: 12498789     DOI: 10.1006/mcne.2002.1196

Source DB:  PubMed          Journal:  Mol Cell Neurosci        ISSN: 1044-7431            Impact factor:   4.314


  58 in total

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Review 4.  Brain dysfunction in the era of combination antiretroviral therapy: implications for the treatment of the aging population of HIV-infected individuals.

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6.  Platelet-derived growth factor protects neurons against gp120-mediated toxicity.

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Review 8.  HIV-1 neuropathogenesis: glial mechanisms revealed through substance abuse.

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9.  Chronic HIV-1 Tat and HIV reduce Rbfox3/NeuN: evidence for sex-related effects.

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10.  Inhibition of human immunodeficiency virus type-1 by cdk inhibitors.

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