The overall aim of this core is to evaluate mechanisms of oxidative injury, inflammation and repair in both the respiratory and cardiovascular systems caused by environmental and occupational agents.
This aim has been a central focus for the core since the 1940?s when Rochester first began investigation into the pulmonary toxicology of airborne particulates. Focus today continues not only on airborne particulates, but also on oxidant gases, endotoxin, siloxanes, zinc oxide and ionizing radiation. Experimental approaches range from basic cellular and molecular methods to animal and clinical human studies. The core studies the impact of inhaled agents in asthma, COPD, fibrosis and lung cancer. Factors that modulate the toxicological effects of inhaled agents, such as age and underlying disease, are also studied. A new approach that has evolved over the last 5 years is the focus on systemic effects of inhaled agents, in particular effects on the cardiovascular system. Nearly 50% of the 181 publications cited since the last renewal are joint authored by members of the core, speaking to the intense collaborative effort underway. The studies carried out by core members result in publications in strong, high-impact scientific journals (AJP Lung, AJRCCM, Environ Health Perspectives, J Immunol, Inhalation Toxicol). All members are now housed under one roof with the construction of a new research building, enhancing the collaborative effort.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Center Core Grants (P30)
Project #
2P30ES001247-31
Application #
6867267
Study Section
Environmental Health Sciences Review Committee (EHS)
Project Start
2005-04-01
Project End
2010-03-31
Budget Start
2005-04-01
Budget End
2006-03-31
Support Year
31
Fiscal Year
2005
Total Cost
$59,634
Indirect Cost
Name
University of Rochester
Department
Type
DUNS #
041294109
City
Rochester
State
NY
Country
United States
Zip Code
14627
Newman, Maureen R; Russell, Steven G; Schmitt, Christopher S et al. (2018) Multivalent Presentation of Peptide Targeting Groups Alters Polymer Biodistribution to Target Tissues. Biomacromolecules 19:71-84
Groves, Angela M; Johnston, Carl J; Williams, Jacqueline P et al. (2018) Role of Infiltrating Monocytes in the Development of Radiation-Induced Pulmonary Fibrosis. Radiat Res 189:300-311
Sobolewski, Marissa; Conrad, Katherine; Marvin, Elena et al. (2018) Endocrine active metals, prenatal stress and enhanced neurobehavioral disruption. Horm Behav 101:36-49
Klocke, Carolyn; Allen, Joshua L; Sobolewski, Marissa et al. (2018) Exposure to fine and ultrafine particulate matter during gestation alters postnatal oligodendrocyte maturation, proliferation capacity, and myelination. Neurotoxicology 65:196-206
McSorley, Emeir M; Yeates, Alison J; Mulhern, Maria S et al. (2018) Associations of maternal immune response with MeHg exposure at 28 weeks' gestation in the Seychelles Child Development Study. Am J Reprod Immunol 80:e13046
Duffney, Parker F; Falsetta, Megan L; Rackow, Ashley R et al. (2018) Key roles for lipid mediators in the adaptive immune response. J Clin Invest 128:2724-2731
Morris-Schaffer, Keith; Sobolewski, Marissa; Allen, Joshua L et al. (2018) Effect of neonatal hyperoxia followed by concentrated ambient ultrafine particle exposure on cumulative learning in C57Bl/6J mice. Neurotoxicology 67:234-244
Willis, Mary D; Jusko, Todd A; Halterman, Jill S et al. (2018) Unconventional natural gas development and pediatric asthma hospitalizations in Pennsylvania. Environ Res 166:402-408
Wahlberg, Karin; Love, Tanzy M; Pineda, Daniela et al. (2018) Maternal polymorphisms in glutathione-related genes are associated with maternal mercury concentrations and early child neurodevelopment in a population with a fish-rich diet. Environ Int 115:142-149
Cholette, Jill M; Pietropaoli, Anthony P; Henrichs, Kelly F et al. (2018) Elevated free hemoglobin and decreased haptoglobin levels are associated with adverse clinical outcomes, unfavorable physiologic measures, and altered inflammatory markers in pediatric cardiac surgery patients. Transfusion 58:1631-1639

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