Dissertation/Thesis Abstract

P-glycoprotein transport in pesticide pharmacokinetics and toxicity: Investigating a link to Parkinson's disease risk
by Lacher, Sarah Elizabeth, Ph.D., University of Montana, 2013, 146; 3597803
Abstract (Summary)

Variation in the gene that encodes P-glycoprotein (P-gp), ABCB1, has been associated with Parkinson's disease risk. The aim of my research was to evaluate P-gp transport of pesticides that have been associated with Parkinson's disease as a mechanism for the pharmacogenomic association. To facilitate this aim, a combination of models was utilized to determine P-gp transport of the pesticides diazinon, dieldrin, endosulfan, maneb, MPP+, paraquat, and rotenone.

Paraquat pharmacokinetics and brain accumulation were measured in both FVB wildtype and mdr1a(-/-)/1b(-/-) mice. P-gp deficient mice displayed no changes in paraquat brain accumulation, indicating that P-gp does not mediate paraquat disposition. I confirmed this observation in vitro using ATPase activity, cytotoxic sensitivity, transepithelial transport, and rhodamine-123 inhibition assays, in which I observed no interaction between P-gp and paraquat. There has been recent controversy regarding paraquat induction of Parkinson's disease in mice. I evaluated paraquat toxicity in both C57BL/6J and FVB wild-type mice. I observed no differences in any of the neurological endpoints in C57BL/6J and FVB mice.

I next evaluated diazinon, dieldrin, endosulfan, maneb, MPP+, and rotenone as P-gp substrates or inhibitors. None of the pesticides inhibited P-gp. Only rotenone stimulated ATPase activity, suggesting that rotenone is a P-gp substrate. It is possible that exposure to rotenone may confer differential Parkinson's disease risk in individuals with genetic variation in ABCB1.

Collectively, I screened the pesticides associated with Parkinson's disease as P-gp substrates and inhibitors. Indentifying rotenone as a P-gp substrate has provided the first piece of evidence towards identifying a potential mechanism for the association between genetic variation in ABCB1 and Parkinson's disease. The observations gathered from the models of P-gp transport and pesticide toxicity evaluated herein will be pivotal in further evaluation of the association of genetic variation in ABCB1 and Parkinson's disease risk. It is possible that this association may be a result of another exposure or endogenous molecule, however, the role of genetic variation in ABCB1 and Parkinson's disease remains unclear. Further, the use of paraquat as a reproducible method to induce Parkinson's disease in mice is an unreliable model of Parkinson's disease and requires further investigation.

Indexing (document details)
Advisor: Woodahl, Erica
Commitee: Cardozo-Pelaez, Fernando, Dickman, Leslie, Poulsen, David, Putnam, Elizabeth, Wetzel, Scott
School: University of Montana
Department: Toxicology
School Location: United States -- Montana
Source: DAI-B 75/01(E), Dissertation Abstracts International
Source Type: DISSERTATION
Subjects: Toxicology, Surgery
Keywords: P-glycoprotein transport, Parkinsons disease, Pesticide, Pharmacokinetics, Toxicity
Publication Number: 3597803
ISBN: 978-1-303-46145-3
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