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Deciphering synaptic perturbations associated with HIV and Metham | 791
Journal of Antivirals & Antiretrovirals

Journal of Antivirals & Antiretrovirals
Open Access

ISSN: 1948-5964

Deciphering synaptic perturbations associated with HIV and Methamphetamine mediated CNS dysfunction


International Conference and Exhibition on VIROLOGY

5-7 September 2011 Baltimore, USA

Gurudutt Pendyala

Scientific Tracks Abstracts: JAA

Abstract :

Drugs of abuse represent a signifi cant co-factor in HIV infection and their synergy can lead to accelerated disorders. With the advent of combined antiretroviral therapy (cART), most severe cognitive impairments are now supplanted by milder, less profound cognitive defi cits that can have signifi cant negative ramifi cations on individuals� activities of daily living. Our research focuses on methamphetamine (METH), a potent psychostimulant and our working hypothesis is that the synaptic molecular composition is altered in HIV infected individuals who use METH. Applying a productive rationale strategy leading to the identifi cation of mechanisms that refl ect cellular responses to HIV/drug abuse, our previous work on quantitative proteomic profi ling on synaptosomes from rhesus caudates identifi ed a potential lead- the neuron specifi c Na+/K+ ATPase alpha 3 subunit (ATP1A3), to be up regulated in the SIV+METH treated group compared to the SIV group. Apart from its well-established role as an ion pump in maintaining electrochemical gradient, emerging studies have implicated ATP1A3 as a receptor for the endogenous steroid ouabain and eliciting signal transduction cascades via MAP kinases especially the ERK1/2 pathway. Examining possible parallels with METH that led to phosphorylation of ERK1/2 from our preliminary data, we hypothesize that a novel mechanism of action of METH in the CNS is to interact with ATP1A3 and elicit signaling. Given the considerable evidence of potential ERK activation with cell survival, proliferation and survival, our current work focuses on defi ning the impact of HIV and METH on ATP1A3 in modulating this biological pathway as well as assessing the functional studies and evaluating the biological consequences in the brain.

Biography :

Dr. Gurudutt Pendyala completed his Ph.D in 2005 from University of Fribourg, Switzerland and postdoctoral training from The Scripps Research Institute. He is currently a Faculty at the University of Nebraska Medical Center since 2009 and serves as a reviewer for 3 peer-reviewed journals including ?omics?-The journal of integrative Biology.

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