Rodent bedding may contain compounds that affect the same endpoints that are the target of NTP's testing program, such as reproduction and development. For example, endotoxins (a byproduct of mold) can mask responses to exposure to asthma-causing agents. We are working with the Quality Assurance Laboratory to quantify these effects and develop guidelines for limits on contaminants in bedding of rodent studies. The ability of acrylamide, a compound found in heated cooking oils, to interfere with reproduction in rodents has been well-established. We fed male mice diets containing either 10% fat or 60% fat, creating groups of lean or obese male mice, respectively. We then showed that obesity in male mice greatly exacerbated the reproductive toxicity of acrylamide. Obese males exposed to acrylamide produced fewer and smaller litters than males that were lean and exposed to acrylamide or that were obese or lean and not exposed to acrylamide. We contributed to the study design of a multi-strain mouse study in which different strains are exposed to ionizing radiation then followed up for development of tumors. These strains were selected to represent a broad range of genetic variation. Although the data are not yet complete, the early indications are that different strains have a range of susceptibility to radiation and show varying locations and rates of tumors.

Project Start
Project End
Budget Start
Budget End
Support Year
14
Fiscal Year
2010
Total Cost
$96,113
Indirect Cost
City
State
Country
Zip Code
Stanko, Jason P; Kissling, Grace E; Chappell, Vesna A et al. (2016) Differences in the Rate of in Situ Mammary Gland Development and Other Developmental Endpoints in Three Strains of Female Rat Commonly Used in Mammary Carcinogenesis Studies: Implications for Timing of Carcinogen Exposure. Toxicol Pathol 44:1021-33
Churchill, Sheba R; Morgan, Daniel L; Kissling, Grace E et al. (2016) Impact of Environmental Enrichment Devices on NTP In Vivo Studies. Toxicol Pathol 44:233-45
French, John E; Gatti, Daniel M; Morgan, Daniel L et al. (2015) Diversity Outbred Mice Identify Population-Based Exposure Thresholds and Genetic Factors that Influence Benzene-Induced Genotoxicity. Environ Health Perspect 123:237-45
Filgo, Adam J; Quist, Erin M; Hoenerhoff, Mark J et al. (2015) Perfluorooctanoic Acid (PFOA)-induced Liver Lesions in Two Strains of Mice Following Developmental Exposures: PPAR? Is Not Required. Toxicol Pathol 43:558-68
Quist, Erin M; Filgo, Adam J; Cummings, Connie A et al. (2015) Hepatic Mitochondrial Alteration in CD-1 Mice Associated with Prenatal Exposures to Low Doses of Perfluorooctanoic Acid (PFOA). Toxicol Pathol 43:546-57
Ramot, Yuval; Kodavanti, Urmila P; Kissling, Grace E et al. (2015) Clinical and pathological manifestations of cardiovascular disease in rat models: the influence of acute ozone exposure. Inhal Toxicol 27 Suppl 1:26-38
Jayes, Friederike L; Burns, Katherine A; Rodriguez, Karina F et al. (2014) The naturally occurring luteinizing hormone surge is diminished in mice lacking estrogen receptor Beta in the ovary. Biol Reprod 90:24
Ray, Mitas; Shockley, Keith; Kissling, Grace (2014) Minimizing Systematic Errors in Quantitative High Throughput Screening Data Using Standardization, Background Subtraction, and Non-Parametric Regression. J Exp Second Sci 3:
Ferguson, Sherry A; Law, Charles Delbert; Kissling, Grace E (2014) Developmental treatment with ethinyl estradiol, but not bisphenol A, causes alterations in sexually dimorphic behaviors in male and female Sprague Dawley rats. Toxicol Sci 140:374-92
Kim, J M; Kosak, J P; Kim, J K et al. (2013) NAG-1/GDF15 transgenic mouse has less white adipose tissue and a reduced inflammatory response. Mediators Inflamm 2013:641851

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