Εμφάνιση απλής εγγραφής

dc.creatorGeorgiadis N., Tsarouhas K., Dorne J.-L.C.M., Kass G.E.N., Laspa P., Toutouzas K., Koulaouzidou E.A., Kouretas D., Tsitsimpikou C.en
dc.date.accessioned2023-01-31T07:40:40Z
dc.date.available2023-01-31T07:40:40Z
dc.date.issued2022
dc.identifier10.3390/jcdd9070226
dc.identifier.issn23083425
dc.identifier.urihttp://hdl.handle.net/11615/72129
dc.description.abstract(1) Background: Human health risks and hazards from chemical substances are well regulated internationally. However, cardiotoxicity, is not defined as a stand-alone hazard and therefore there are no defined criteria for the classification of substances as cardiotoxic. Identifying and regulating substances that cause cardiovascular adverse effects would undoubtedly strengthen the national health systems. (2) Methods: To overcome the aforementioned gap, a roadmap is proposed for identifying regulatory criteria from animal studies and endorse legislation in order to classify substances as cardiotoxic. The roadmap consists of: (i) the identification of the appropriate animal species and strains; (ii) the identification of the lines of scientific evidence (e.g., histopathological, biochemical and echocardiographic indices etc.) from animal studies with relevance to humans; (iii) the statistical analysis and meta-analysis for each line of scientific evidence after exposure to well-established cardiotoxicants to humans (e.g., anthracyclines) in order to identify threshold values or range of normal and/ or altered values due to exposure; (iv) validation of the above described lines of evidence in animals exposed to other alleged cardiotoxic substances (e.g., anabolic androgen steroids (AAS) and pesticides); (v) establishment of mechanisms of action based on information of either known or alleged cardiotoxicants; and (vi) introduction of novel indices and in silico methods. (3) Results: Preliminary results in rats indicate a clear distinction from normal values to values measured in rats exposed to anthracyclines regarding left ventricle (LV) fractional shortening (FS) and LV ejection fraction (EF). A distinctive pattern is similarly observed for Creatine Kinase-Myocardial Band isoenzyme (CK-MB) and cardiac tissue glutathione (GSH). These findings are encouraging and indicate that there is room for targeted research to this end, and that these specific indices and biochemical markers should be further investigated in order to be developed to regulatory criteria. (4) Conclusions: Further research should be conducted by both the scientific and regulatory community that aims to clearly define the cardiotoxicity hazard caused by chemicals and develop a full set of scientific criteria. © 2022 by the authors.en
dc.language.isoenen
dc.sourceJournal of Cardiovascular Development and Diseaseen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85135526063&doi=10.3390%2fjcdd9070226&partnerID=40&md5=f615816e2d8ab3044a378c9d97274839
dc.subjectanthracyclineen
dc.subjectbiochemical markeren
dc.subjectbiological markeren
dc.subjectcatalaseen
dc.subjectcreatine kinase MBen
dc.subjectdaunorubicinen
dc.subjectdoxorubicinen
dc.subjectepirubicinen
dc.subjectglutathioneen
dc.subjectglutathione peroxidaseen
dc.subjectidarubicinen
dc.subjectisoenzymeen
dc.subjectmalonaldehydeen
dc.subjectpesticideen
dc.subjectcardiotoxicityen
dc.subjectcomputer modelen
dc.subjectcontrolled studyen
dc.subjectechocardiographyen
dc.subjectheart left ventricle ejection fractionen
dc.subjectheart tissueen
dc.subjecthistopathologyen
dc.subjectlawen
dc.subjectleft ventricular fractional shorteningen
dc.subjectmaleen
dc.subjectmeta analysisen
dc.subjectnonhumanen
dc.subjectnormal valueen
dc.subjectpreliminary dataen
dc.subjectpublic healthen
dc.subjectraten
dc.subjectReviewen
dc.subjectrisk assessmenten
dc.subjectvalidation processen
dc.subjectMDPIen
dc.titleCardiotoxicity of Chemical Substances: An Emerging Hazard Classen
dc.typeotheren


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