Chronic exposure to polychlorinated biphenyls (PCBs) has been associated with a wide range of toxic effects, including hepatotoxicity, carcinogenicity, hormonal disruption, and neurotoxicity. The persistence of PCBs in the environment combined with their """"""""bioaccumulative"""""""" nature make PCBs a significant health hazard in highly contaminated areas, even though U.S. production was banned in 1977. Recent research has demonstrated that PCBs and PCB metabolites can increase mitochondrial dysfunction and cause oxidative injury via increases in mitochondrial superoxide and hydrogen peroxide, suggesting that mitochondria are a major target. Sirtuin 3 (Sirt3), which is the major deacetylase in mammalian mitochondria, has been linked to the regulation of the mitochondrial acetylome and activation of several metabolic enzymes (e.g., MnSOD) in response to environmental stresses. Furthermore, loss of function of this mitochondrial fidelity protein appears to enhance the injury processes induced by stress by contributing to aberrant oxidative metabolism and genomic instability in vitro and in vivo. Therefore, the goal of the current application is to determine whether Sirt3 activity can protect against PCB-induced mitochondrial dysfunction, oxidative stress, and tissue injury. In pursuit of this goal, we will rigorously test he hypothesis that Sirt3 function regulates the alterations in the mitochondrial acetylome to maintain oxidative homeostasis in response to PCB-induced mitochondrial injury through the following specific aims.
In Aim 1, we will determine if loss of Sirt3 function disrupts the maintenance of the mitochondrial acetylome in response to PCB-induced mitochondrial dysfunction and oxidative stress. Thus, this aim will determine whether loss of Sirt3 function enhances PCB-induced mitochondrial dysfunction (Aim 1a) and oxidative stress (Aim 1b) and whether exposure to PCBs alters the Sirt3 acetylation targets responsible for protecting oxidative homeostasis in the mitochondrial acetylome (Aim 1c).
In Aim 2, we will determine if Sirt3 protects against PCB-induced mitochondrial injury by directing MnSOD activity via post-translational modification of critical acetyl lysines (Aim 2a) and whether the changes in acetylation status of critical lysines in MnSOD modulate PCB-induced mitochondrial dysfunction (Aim 2b).
In Aim 3, we will determine if the changes in mitochondrial function following PCB exposure result in differential expression of mitochondria-related genes in the livers of Sirt3+/+ and Sirt3-/- mice. Successful completion of these specific aims will contribute to the mechanistic understanding of the role of a mitochondrial fidelity protein, Sirt3, in tissue injury and mitochondrial dysfunction with potential identification of novel targets for pharmacologic manipulation for the health problems arising from PCB exposure. The information to be gained from the proposed studies will also advance the mission of the NIEHS to reduce the burden of human illness and dysfunction from environmental causes. Furthermore, this application will provide biomedical research experience for undergraduate and graduate students in line with the AREA program objectives.

Public Health Relevance

Chronic exposure to polychlorinated biphenyls (PCBs) in the environment has been associated with a wide range of toxic effects, making them a significant health hazard in highly contaminated areas, because they persist in the environment and can bioaccumulate. This proposal seeks to understand the mechanisms of how PCBs induce dysfunction, oxidative stress, and injury to the mitochondria, which produce chemical energy to power the cell and are involved in a range of other processes, including control of the cell cycle and cell growth. The goal of the proposed studies is to establish a link between an enzyme (the deacetylase Sirt3) produced by mitochondria and PCB-induced mitochondrial injury, thus has the potential to identify novel drug targets that would ameliorate the health problems arising from PCB exposure.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Academic Research Enhancement Awards (AREA) (R15)
Project #
1R15ES022781-01
Application #
8496911
Study Section
Special Emphasis Panel (ZRG1-DKUS-C (90))
Program Officer
Shaughnessy, Daniel
Project Start
2013-09-13
Project End
2016-08-31
Budget Start
2013-09-13
Budget End
2016-08-31
Support Year
1
Fiscal Year
2013
Total Cost
$442,500
Indirect Cost
$142,500
Name
University of Arkansas for Medical Sciences
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
122452563
City
Little Rock
State
AR
Country
United States
Zip Code
72205
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Banerjee, Sudip; Melnyk, Stepan B; Krager, Kimberly J et al. (2015) The neuronal nitric oxide synthase inhibitor NANT blocks acetaminophen toxicity and protein nitration in freshly isolated hepatocytes. Free Radic Biol Med 89:750-7
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