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Statins: an undesirable class of aquatic contaminants?

dc.contributor.authorSantos, Miguel M.
dc.contributor.authorRuivo, Raquel
dc.contributor.authorLopes-Marques, Mónica
dc.contributor.authorTorres, Tiago
dc.contributor.authorde los Santos, Carmen B.
dc.contributor.authorCastro, L. Filipe C.
dc.contributor.authorNeuparth, Teresa
dc.date.accessioned2022-03-03T15:02:05Z
dc.date.available2022-03-03T15:02:05Z
dc.date.issued2016-05
dc.date.updated2022-03-03T12:13:25Z
dc.description.abstractEmerging pollutants, such as pharmaceuticals, may pose a considerable environment risk. Hypocholesterolaemic drugs such as statins are among the most prescribed human pharmaceuticals in western European countries. In vertebrates, this therapeutic class disrupts the cholesterol synthesis by inhibiting the enzyme 3-hydroxy-3-methyl-glutaryl-CoA reductase (HMGR), responsible for the limiting step in the mevalonate pathway. Recently, functional studies have shown that statins competitively inhibit HMGR in vertebrates and arthropods, two taxa that have diverged over 450 million years ago. Importantly, chronic simvastatin exposure disrupts crustacean reproduction and development at environmentally relevant concentrations. Hence, a fundamental question emerges: what is the taxonomic scope of statins-induced HMGR inhibition across metazoans? Here, we address this central question in a large sampling of metazoans using comparative genomics, homology modelling and molecular docking. Sequence alignment of metazoan HMGRs allowed the annotation of highly conserved catalytic, co-factor and substrate binding sites, including residues highjacked for statin binding. Furthermore, molecular docking shows that the catalytic domains of metazoan HMGRs are highly conserved regarding interactions, not only with HMG-CoA, but also with both simvastatin and atorvastatin, the top prescribed statins in Europe and USA. Hence, the data indicates that both statins are expected to competitively inhibit metazoan’s HMGRs, and therefore all metazoan taxa might be at risk. The environmental relevance of these findings are discussed and research priorities established. We believe that the conceptual framework used in this study can be applied to other emerging pollutants and assist in the design of toxicity testing and risk assessment.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.doi10.1016/j.aquatox.2016.02.001pt_PT
dc.identifier.issn0166-445X
dc.identifier.slugcv-prod-938602
dc.identifier.urihttp://hdl.handle.net/10400.1/17626
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherElsevierpt_PT
dc.subjectStatinspt_PT
dc.subjectRisk assessmentpt_PT
dc.subjectEmerging pollutant In silicopt_PT
dc.subjectToxicity testingpt_PT
dc.subjectMode of action (MOA)pt_PT
dc.titleStatins: an undesirable class of aquatic contaminants?pt_PT
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage9pt_PT
oaire.citation.startPage1pt_PT
oaire.citation.titleAquatic Toxicologypt_PT
oaire.citation.volume174pt_PT
person.familyNameBarrena de los Santos
person.givenNameCarmen
person.identifier.ciencia-idC317-02C0-516E
person.identifier.orcid0000-0002-7013-494X
person.identifier.ridL-3723-2014
person.identifier.scopus-author-id26427612000
rcaap.cv.cienciaidC317-02C0-516E | Carmen B de los Santos
rcaap.rightsrestrictedAccesspt_PT
rcaap.typearticlept_PT
relation.isAuthorOfPublication9df095b9-2b1c-4f05-a3f9-afb40706adff
relation.isAuthorOfPublication.latestForDiscovery9df095b9-2b1c-4f05-a3f9-afb40706adff

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