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dc.creatorDardiotis E., Aloizou A.-M., Siokas V., Tsouris Z., Rikos D., Marogianni C., Aschner M., Kovatsi L., Bogdanos D.P., Tsatsakis A.en
dc.date.accessioned2023-01-31T07:50:38Z
dc.date.available2023-01-31T07:50:38Z
dc.date.issued2019
dc.identifier10.1016/j.tox.2018.10.012
dc.identifier.issn0300483X
dc.identifier.urihttp://hdl.handle.net/11615/73078
dc.description.abstractOrganophosphates (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.en
dc.language.isoenen
dc.sourceToxicologyen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85055625689&doi=10.1016%2fj.tox.2018.10.012&partnerID=40&md5=f282d8b92c52d88aeb7cc7ecd670f5b6
dc.subjectaryldialkylphosphatase 1en
dc.subjectorganophosphateen
dc.subjectaryldialkylphosphataseen
dc.subjectorganophosphateen
dc.subjectpesticideen
dc.subjectPON1 protein, humanen
dc.subjectArticleen
dc.subjectbiosynthesisen
dc.subjectcell damageen
dc.subjectconsensusen
dc.subjectenzyme activityen
dc.subjectenzyme metabolismen
dc.subjectgenetic polymorphismen
dc.subjectgenetic susceptibilityen
dc.subjectgenetic toxicologyen
dc.subjectgenotypeen
dc.subjecthumanen
dc.subjectMedlineen
dc.subjectorganophosphate poisoningen
dc.subjectprevalenceen
dc.subjectpriority journalen
dc.subjectanimalen
dc.subjectgene frequencyen
dc.subjectgenetic polymorphismen
dc.subjectgeneticsen
dc.subjectmetabolismen
dc.subjectAnimalsen
dc.subjectAryldialkylphosphataseen
dc.subjectGene Frequencyen
dc.subjectHumansen
dc.subjectOrganophosphatesen
dc.subjectPesticidesen
dc.subjectPolymorphism, Geneticen
dc.subjectElsevier Ireland Ltden
dc.titleParaoxonase-1 genetic polymorphisms in organophosphate metabolismen
dc.typejournalArticleen


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