The overall goal of this project is to examine whether exposure to environmental pollutants, specifically volatile organic compounds (VOCs), induces/exacerbates cardiometabolic disease (CMD) by causing systemic insulin resistance and low grade inflammation. Insulin is a master regulator of metabolism and energy disposition, and dysregulation of insulin signaling is associated with the development of obesity and Type 2 diabetes (T2D), which are robust contributors to atherogenesis and heart disease. Recent research has identified a pathogenic continuum between the development of insulin resistance, hepatic steatosis, dyslipidemia and cardiovascular disease. We postulate that environmental pollutants/toxins can either directly cause CMD or interact with obesity and poor nutrition to cause/exacerbate CMD. We have published initial experimental human/rodent data to support this concept, and further preliminary animal data are presented in Project #2. Here, we present important human preliminary results from a unique database/specimen bank of plant workers exposed to high levels of certain VOCs, especially vinyl chloride. The Toxicology Specimen and Databank provides the opportunity for a novel cross-sectional study evaluating the effects of vinyl chloride and other VOCs on the development of insulin resistance and fatty liver (Aim 1a). We will examine our death certificate data to evaluate the effects of VOC exposure on all cause and cardiac deaths (Aim 1b). We will also perform a retrospective/prospective study using samples obtained over a ~40-year period of time to correlate the development of insulin resistance with outcome measures of the CMD and predictors of risk (including occupational exposure, personal exposure, and novel markers of metabolic injury that we have developed? Aim 1c). We will also be able to enroll residents from VOC hot spots including the Lees Lane superfund site in a prospective longitudinal evaluation of the impact of lower levels of exposure and the impact of obesity/nutrition on the progression of CMD (Aim 2). We are able to perform these studies because of an established database, continued linkages with industry for nearly 40 years, and ongoing interactions with community leaders and residents which provide a highly-novel opportunity to assess the cardiometabolic effects of VOCs over a range of exposures.

Public Health Relevance

The overall goal of this project is to examine whether exposure to environmental pollutants, particularly volatile organic compounds (VOCs), causes, or makes worse, a group of disease processes known as cardiometabolic disease (CMD). These processes include type 2 diabetes, cardiovascular disease and fatty liver disease. All of these conditions seem to be regulated through insulin resistance. We hypothesize that environmental pollutants/toxins can either directly cause CMD or interact with obesity and poor nutrition to cause CMD or make it worse. In this project, we will investigate subjects from two ongoing studies?Occupational Toxicology Data and Specimen Bank and the Louisville Healthy Heart Study?to determine if exposure to pollutants leads to insulin resistance, and subsequent CMD. We are able to perform these studies because of an established database, continued linkages with industry for nearly 40 years, and ongoing interactions with community leaders and residents which provide a highly-novel opportunity to assess the effects of pollutants in both workers and a residential population from the same West Louisville area.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Hazardous Substances Basic Research Grants Program (NIEHS) (P42)
Project #
5P42ES023716-02
Application #
9554903
Study Section
Special Emphasis Panel (ZES1)
Project Start
Project End
Budget Start
2018-04-01
Budget End
2019-03-31
Support Year
2
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Louisville
Department
Type
DUNS #
057588857
City
Louisville
State
KY
Country
United States
Zip Code
40292
Lang, Anna L; Chen, Liya; Poff, Gavin D et al. (2018) Vinyl chloride dysregulates metabolic homeostasis and enhances diet-induced liver injury in mice. Hepatol Commun 2:270-284
Xie, Zhenzhen; Ramakrishnam Raju, Mandapati V; Stewart, Andrew C et al. (2018) Imparting sensitivity and selectivity to a gold nanoparticle chemiresistor through thiol monolayer functionalization for sensing acetone. RSC Adv 8:35618-35624
Lang, Anna L; Beier, Juliane I (2018) Interaction of volatile organic compounds and underlying liver disease: a new paradigm for risk. Biol Chem 399:1237-1248
Riggs, Daniel W; Yeager, Ray A; Bhatnagar, Aruni (2018) Defining the Human Envirome: An Omics Approach for Assessing the Environmental Risk of Cardiovascular Disease. Circ Res 122:1259-1275
Li, Mingxiao; Li, Qi; Nantz, Michael H et al. (2018) Analysis of Carbonyl Compounds in Ambient Air by a Microreactor Approach. ACS Omega 3:6764-6769
Hein, David W; Zhang, Xiaoyan; Doll, Mark A (2018) Role of N-acetyltransferase 2 acetylation polymorphism in 4, 4'-methylene bis (2-chloroaniline) biotransformation. Toxicol Lett 283:100-105
Hein, David W; Fakis, Giannoulis; Boukouvala, Sotiria (2018) Functional expression of human arylamine N-acetyltransferase NAT1*10 and NAT1*11 alleles: a mini review. Pharmacogenet Genomics 28:238-244
Liang, Yaqin; Lang, Anna L; Zhang, Jian et al. (2018) Exposure to Vinyl Chloride and Its Influence on Western Diet-Induced Cardiac Remodeling. Chem Res Toxicol 31:482-493
Ramana, Kota V; Srivastava, Sanjay; Singhal, Sharad S (2017) Lipid Peroxidation Products in Human Health and Disease 2016. Oxid Med Cell Longev 2017:2163285
Ramana, Kota V; Srivastava, Sanjay; Reddy, Aramati B M (2016) Immune, Inflammatory, and Oxidative Responses in Cardiovascular Complications. Oxid Med Cell Longev 2016:6858402

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