This subproject is one of many research subprojects utilizing the resources provided by a Center grant funded by NIH/NCRR. The subproject and investigator (PI) may have received primary funding from another NIH source, and thus could be represented in other CRISP entries. The institution listed is for the Center, which is not necessarily the institution for the investigator. The goal of this research is to develop a human brain cell model to evaluate the mitochondrial effects of human equivalent doses of HIV antiretroviral medications. Our hypothesis is that antiretroviral drugs are contributing to mitochondrial dysfunction of neurons by decreasing energy metabolism and increasing oxidative stress. We propose to examine this hypothesis by treating primary human neuronal cells with human equivalent drug doses used in antiretroviral therapy and evaluating mitochondrial DNA and RNA levels, ATP production, and mitochondrial specific oxidative damage and antioxidants.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
2P20RR016467-09A1
Application #
8168067
Study Section
Special Emphasis Panel (ZRR1-RI-7 (01))
Project Start
2010-08-01
Project End
2011-05-31
Budget Start
2010-08-01
Budget End
2011-05-31
Support Year
9
Fiscal Year
2010
Total Cost
$323,567
Indirect Cost
Name
University of Hawaii
Department
Type
Schools of Medicine
DUNS #
965088057
City
Honolulu
State
HI
Country
United States
Zip Code
96822
Kaholokula, Joseph Keawe'aimoku; Antonio, Mapuana C K; Ing, Claire K Townsend et al. (2017) The effects of perceived racism on psychological distress mediated by venting and disengagement coping in Native Hawaiians. BMC Psychol 5:2
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Panee, Jun; Pang, Xiaosha; Munsaka, Sody et al. (2015) Independent and co-morbid HIV infection and Meth use disorders on oxidative stress markers in the cerebrospinal fluid and depressive symptoms. J Neuroimmune Pharmacol 10:111-21
Rueli, Rachel H L H; Parubrub, Arlene C; Dewing, Andrea S T et al. (2015) Increased selenoprotein P in choroid plexus and cerebrospinal fluid in Alzheimer's disease brain. J Alzheimers Dis 44:379-83
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