Abstract:
:Although the causes of Parkinson's disease (PD) are not fully understood, the consensus is that a combination of genetic and environmental factors plays a major role. The discovery that the synthetic chemical, 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP)-derived N-methyl-4-phenylpyridinium (MPP+), recapitulates major pathophysiological characteristics of PD in humans and other mammals has provided the strongest support for this possibility; however, several key aspects of the mechanism remain unclear. In contrast to the widely accepted view that MPP+ is structurally unique and optimal for selective dopaminergic toxicity, previous in vitro studies have suggested that MPP+ is most likely a simple member of a large group of related dopaminergic toxins. Here we provide first in vivo evidence to support the above possibility using Caenorhabditis elegans PD models. We also provide in vivo evidence to show that the inherent predisposition of dopaminergic neurons to produce high oxidative stress and related downstream effects when exposed to MPP+ and related mitochondrial toxins is responsible for their selective vulnerability to these toxins. More significantly, present findings suggest that if this broad group of MPP+ related dopaminergic toxins are present in work places or in the environment, they could cause far-reaching public health consequences.
journal_name
Chem Res Toxicoljournal_title
Chemical research in toxicologyauthors
Murphy D,Patel H,Wimalasena Kdoi
10.1021/acs.chemrestox.0c00422subject
Has Abstractpub_date
2021-01-26 00:00:00eissn
0893-228Xissn
1520-5010pub_type
杂志文章abstract::Estrogens and their oxidative metabolites, the catechol estrogens, have been implicated in the development of breast cancer; yet, relatively little is known about estrogen metabolism in the breast. To determine how the parent hormone, 17 beta-estradiol (E(2)), is metabolized, we used recombinant, purified phase I enzy...
journal_title:Chemical research in toxicology
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journal_title:Chemical research in toxicology
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journal_title:Chemical research in toxicology
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journal_title:Chemical research in toxicology
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pub_type: 杂志文章,评审
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journal_title:Chemical research in toxicology
pub_type: 杂志文章
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journal_title:Chemical research in toxicology
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journal_title:Chemical research in toxicology
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journal_title:Chemical research in toxicology
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更新日期:2006-08-01 00:00:00
abstract::Isoeugenol is widely used by the cosmetic and fragrance industries, but it also represents a known cause of skin sensitization adverse effects. Although devoid of a structural alert, isoeugenol has been classified as prehapten in virtue of the presence of a pre-Michael acceptor domain. Isoeugenol oxidation could theor...
journal_title:Chemical research in toxicology
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更新日期:2020-04-20 00:00:00