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Oxidative Stress and Analysis of Selected SNPs ofACHE(rs 2571598),BCHE(rs 3495),CAT(rs 7943316),SIRT1(rs 10823108),GSTP1(rs 1695), and GeneGSTM1,GSTT1in Chronic Organophosphates Exposed Groups from Cameroon and Pakistan

dc.contributor.authorNtepe, Leonel Javeres Mbah
dc.contributor.authorHabib, Rabia
dc.contributor.authorLaure, Ngondi Judith
dc.contributor.authorRaza, Saqlain
dc.contributor.authorNepovimová, Eugenie
dc.contributor.authorKuča, Kamil
dc.contributor.authorBatool, Sajida
dc.contributor.authorNurulain, Syed Muhammad
dc.date.accessioned2025-12-05T09:16:37Z
dc.date.available2025-12-05T09:16:37Z
dc.date.issued2020
dc.description.abstractThe detrimental effects of organophosphates (OPs) on human health are thought to be of systemic, i.e., irreversible inhibition of acetylcholinesterase (AChE) at nerve synapses. However, several studies have shown that AChE inhibition alone cannot explain all the toxicological manifestations in prolonged exposure to OPs. The present study aimed to assess the status of antioxidants malondialdehyde (MDA), superoxide dismutase (SOD), glutathione (GSH) (reduced), catalase, and ferric reducing antioxidant power (FRAP) in chronic OP-exposed groups from Cameroon and Pakistan. Molecular analysis of genetic polymorphisms (SNPs) of glutathione transferases (GSTM1, GSTP1, GSTT1), catalase gene (CAT, rs7943316), sirtuin 1 gene (SIRT1, rs10823108), acetylcholinesterase gene (ACHE, rs2571598), and butyrylcholinesterase gene (BCHE, rs3495) were screened in the OP-exposed individuals to find the possible causative association with oxidative stress and toxicity. Cholinesterase and antioxidant activities were measured by colorimetric methods using a spectrophotometer. Salting-out method was employed for DNA extraction from blood followed by restriction fragment length polymorphism (RFLP) for molecular analysis. Cholinergic enzymes were significantly decreased in OP-exposed groups. Catalase and SOD were decreased and MDA and FRAP were increased in OP-exposed groups compared to unexposed groups in both groups. GSH was decreased only in Pakistani OPs-exposed group. Molecular analysis of ACHE, BCHE, Catalase, GSTP1, and GSTM1 SNPs revealed a tentative association with their phenotypic expression that is level of antioxidant and cholinergic enzymes. The study concludes that chronic OPs exposure induces oxidative stress which is associated with the related SNP polymorphism. The toxicogenetics of understudied SNPs were examined for the first time to our understanding. The findings may lead to a newer area of investigation on OPs induced health issues and toxicogenetics.eng
dc.formatp. &quot;Article Number: 6432&quot;
dc.identifier.doi10.3390/ijms21176432
dc.identifier.issn1422-0067
dc.identifier.obd43876718
dc.identifier.urihttp://hdl.handle.net/20.500.12603/1079
dc.identifier.wos000569794600001
dc.language.isoeng
dc.peerreviewedyes
dc.publicationstatuspostprint
dc.publisherMDPI
dc.relation.ispartofINTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, volume 21, issue: 17eng
dc.relation.publisherversionhttps://www.mdpi.com/1422-0067/21/17/6432
dc.rights.accessOpen Access
dc.rights.licenseCC BY
dc.source.urlhttps://www.mdpi.com/1422-0067/21/17/6432
dc.subjectorganophosphateseng
dc.subjectantioxidantseng
dc.subjectcholinergic enzymeseng
dc.subjectSNPseng
dc.subjecttoxicogeneticseng
dc.titleOxidative Stress and Analysis of Selected SNPs ofACHE(rs 2571598),BCHE(rs 3495),CAT(rs 7943316),SIRT1(rs 10823108),GSTP1(rs 1695), and GeneGSTM1,GSTT1in Chronic Organophosphates Exposed Groups from Cameroon and Pakistaneng
dc.typearticle

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