Date on Master's Thesis/Doctoral Dissertation
5-2018
Document Type
Master's Thesis
Degree Name
M.S.
Department
Pharmacology and Toxicology
Degree Program
Pharmacology and Toxicology, MS
Committee Chair
Arteel, Gavin
Committee Co-Chair (if applicable)
Cai, Lu
Committee Member
Cai, Lu
Committee Member
States, J. Christopher
Committee Member
Merchant, Michael
Committee Member
Neal, Rachel
Author's Keywords
in utero; metabolic syndrome; NAFLD; arsenic; cadmium; gender differences
Abstract
Metabolic syndrome (MetS) is a group of diseases affecting < 30% of adults. Although obesity is a major risk for the development of MetS, it does not account for all cases, suggesting contribution of other risk factors. We hypothesized that early life exposure to arsenic (As) or cadmium (Cd) may represent such a risk. The purpose of this study was to characterize a model to discern the effects of early life exposures to Cd and As on high fat diet (HFD)-induced MetS. Adult C57BL/6J mice were exposed to control or metals containing drinking water. Pregnant dams and offspring were continuously exposed to the same toxicants as their parents. At weaning, offspring were fed LFD or HFD and sacrificed 10 or 24 weeks later. Metal exposure caused time- and sex-dependent alterations in HFD-induced variables of liver damage. The initial results suggest that these toxicants enhanced obesity-induced liver injury.
Recommended Citation
Young, Jamie L., "A model to study the effects of whole life chronic exposure to arsenic or cadmium on the development of adult metabolic syndrome : initial characterization of hepatic changes." (2018). Electronic Theses and Dissertations. Paper 2959.
https://doi.org/10.18297/etd/2959
