This application requests funds for support of biomedical and ecoengineering research directed toward a better understanding of the potential human health hazards arising from contamination of groundwater with volatile organic compounds (VOCs) and for remediation of this situation. A group of twenty-one scientists from Michigan State University and the University of Michigan propose to conduct collaborative research on ten different projects connected with VOC contamination of groundwater caused by leaking waste storage sites. Research connected with remediation of contamination will include studies of the ability of microorganisms to degrade VOCs and the engineering- based application of biodegradation process used alone or in connection with adsorptive processes. Other studies will involve measurement of the retention properties of clays and modified clays, and the abilities of these materials to catalyze chemical degradation of VOCs. The transport of volatile contaminants in soils and groundwater will be studied experimentally and refined mathematical models describing this movement will be developed for use in predicting time courses of contamination and clean-up. Biomedical scientists will study the effects of VOCs on membrane- connected functions associated with important biological processes. Included will be studies of VOC effects on biomembrane structure, activated neutrophil involvement in toxicity, gamete function and embryonic growth, cell-cell communication, in addition to VOC-induced changes in oncogene expression and possible roles in cancer promotion. The results of this research will be used to help clarify the health hazards of various VOCs and to direct the remediation research to encompass VOCs that may cause the greatest health-related concerns. This research effort will be accompanied by a training component designed to give physical/chemical oriented graduate students sufficient toxicological knowledge to facilitate their careers in research directed toward remediation of environmental contamination by hazardous chemicals.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Hazardous Substances Basic Research Grants Program (NIEHS) (P42)
Project #
5P42ES004911-03
Application #
3104484
Study Section
Special Emphasis Panel (SRC (02))
Project Start
1988-12-07
Project End
1992-03-31
Budget Start
1990-12-01
Budget End
1992-03-31
Support Year
3
Fiscal Year
1991
Total Cost
Indirect Cost
Name
Michigan State University
Department
Type
Organized Research Units
DUNS #
193247145
City
East Lansing
State
MI
Country
United States
Zip Code
48824
Konganti, Kranti; Ehrlich, Andre; Rusyn, Ivan et al. (2018) gQTL: A Web Application for QTL Analysis Using the Collaborative Cross Mouse Genetic Reference Population. G3 (Bethesda) 8:2559-2562
Zhang, Shuai; Liu, Qinfu; Gao, Feng et al. (2018) Molecular Dynamics Simulation of Basal Spacing, Energetics, and Structure Evolution of a Kaolinite-Formamide Intercalation Complex and Their Interfacial Interaction. J Phys Chem C Nanomater Interfaces 122:3341-3349
Nault, Rance; Doskey, Claire M; Fader, Kelly A et al. (2018) Comparison of Hepatic NRF2 and Aryl Hydrocarbon Receptor Binding in 2,3,7,8-Tetrachlorodibenzo-p-dioxin-Treated Mice Demonstrates NRF2-Independent PKM2 Induction. Mol Pharmacol 94:876-884
Dornbos, Peter; LaPres, John J (2018) Incorporating population-level genetic variability within laboratory models in toxicology: From the individual to the population. Toxicology 395:1-8
Zhang, Shuai; Liu, Qinfu; Gao, Feng et al. (2018) Interfacial Structure and Interaction of Kaolinite Intercalated with N-methylformamide Insight from Molecular Dynamics Modeling. Appl Clay Sci 158:204-210
Fader, Kelly A; Nault, Rance; Raehtz, Sandi et al. (2018) 2,3,7,8-Tetrachlorodibenzo-p-dioxin dose-dependently increases bone mass and decreases marrow adiposity in juvenile mice. Toxicol Appl Pharmacol 348:85-98
Zhang, Shuai; Liu, Qinfu; Cheng, Hongfei et al. (2018) Mechanism Responsible for Intercalation of Dimethyl Sulfoxide in Kaolinite: Molecular Dynamics Simulations. Appl Clay Sci 151:46-53
Zhang, Qiang; Li, Jin; Middleton, Alistair et al. (2018) Bridging the Data Gap From in vitro Toxicity Testing to Chemical Safety Assessment Through Computational Modeling. Front Public Health 6:261
Fader, K A; Nault, R; Kirby, M P et al. (2018) Corrigendum to ""Convergence of hepcidin deficiency, systemic iron overloading, heme accumulation, and REV-ERB?/? activation in aryl hydrocarbon receptor-elicited hepatotoxicity"" [Toxicol. Appl. Pharmacol. 321 (2017) 1-17]. Toxicol Appl Pharmacol 344:74
Williams, M R; Stedtfeld, R D; Waseem, H et al. (2017) Implications of direct amplification for measuring antimicrobial resistance using point-of-care devices. Anal Methods 9:1229-1241

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