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  •   Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
  • Επιστημονικές Δημοσιεύσεις Μελών ΠΘ (ΕΔΠΘ)
  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ.
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Ιδρυματικό Αποθετήριο Πανεπιστημίου Θεσσαλίας
Όλο το DSpace
  • Κοινότητες & Συλλογές
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Paraoxonase-1 genetic polymorphisms in organophosphate metabolism

Thumbnail
Συγγραφέας
Dardiotis E., Aloizou A.-M., Siokas V., Tsouris Z., Rikos D., Marogianni C., Aschner M., Kovatsi L., Bogdanos D.P., Tsatsakis A.
Ημερομηνία
2019
Γλώσσα
en
DOI
10.1016/j.tox.2018.10.012
Λέξη-κλειδί
aryldialkylphosphatase 1
organophosphate
aryldialkylphosphatase
organophosphate
pesticide
PON1 protein, human
Article
biosynthesis
cell damage
consensus
enzyme activity
enzyme metabolism
genetic polymorphism
genetic susceptibility
genetic toxicology
genotype
human
Medline
organophosphate poisoning
prevalence
priority journal
animal
gene frequency
genetic polymorphism
genetics
metabolism
Animals
Aryldialkylphosphatase
Gene Frequency
Humans
Organophosphates
Pesticides
Polymorphism, Genetic
Elsevier Ireland Ltd
Εμφάνιση Μεταδεδομένων
Επιτομή
Organophosphates (OPs) are a class of chemicals commonly used in agriculture as pesticides, that can often lead to severe toxicity in humans. Paraoxonase-1 (PON1) belongs to a family of A-esterases and hydrolyses several OPs while also serving other biological roles. Two main genetic polymorphisms have been shown to affect enzymatic ability; an A > G transition in the 192nd position (192 Q/R, rs662), and an A > T at codon 55 (55 M/L, rs854560). In this review, we searched PubMed for relevant articles published from its inception till June 2018 and included publications from 1996 to 2018. We aimed to address the distribution of the polymorphisms in various populations, the way they affect enzymatic activity and the possible use of PON1 as a biomarker. The polymorphisms present great heterogeneity between populations, with the data being clearer over 192 Q/R, and this heterogeneity is related to the phylogenetic origins of each population. Concerning enzymatic activity, the different genotypes react better or worse to different OP substrates, with studies presenting a variety of findings. Detecting the “paraoxonase status” of an individual -referring to PON1 function- seems to be important in predicting OP toxicity, as studies have shown that some specific-genotype individuals present symptoms of toxicity in higher rates than others. We are strongly convinced that in order for the scientific community to reach a consensus over which polymorphisms confer susceptibility to toxicity and whether PON1 can eventually be used as a biomarker, more studies need to be carried out, since the data thus far does not seem to reach a universal conclusion. © 2018 Elsevier B.V.
URI
http://hdl.handle.net/11615/73078
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  • Δημοσιεύσεις σε περιοδικά, συνέδρια, κεφάλαια βιβλίων κλπ. [19674]

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Με τη συγχρηματοδότηση της Ελλάδας και της Ευρωπαϊκής Ένωσης
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