2019
DOI: 10.1007/s00204-019-02628-x
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Developmental toxicity of arsenic: a drift from the classical dose–response relationship

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Cited by 23 publications
(8 citation statements)
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“…Our study has confirmed the prolongation of QT interval as a major complication of As exposure 40–42 . Blocking potassium channels by As increases the risk of excessive repolarization delay in phase 3 of the cardiac action potential, causing changes in ventricular action potential duration (APD) 43 . Increased APD is reflected by prolongation of the QT interval, displaying ventricular depolarization and repolarization 44 .…”
Section: Discussionsupporting
confidence: 71%
“…Our study has confirmed the prolongation of QT interval as a major complication of As exposure 40–42 . Blocking potassium channels by As increases the risk of excessive repolarization delay in phase 3 of the cardiac action potential, causing changes in ventricular action potential duration (APD) 43 . Increased APD is reflected by prolongation of the QT interval, displaying ventricular depolarization and repolarization 44 .…”
Section: Discussionsupporting
confidence: 71%
“…Depending on exposure levels and circumstances, various health consequences are observed, such as skin rashes and pulmonary and cardiovascular diseases. Children and infants exposed to arsenic frequently develop neuro-developmental and -behavioral disorders [43,44].…”
Section: Table 3 Toxic Hazardsmentioning
confidence: 99%
“… 3 iAs and its metabolites can cross the placenta, 25 and fetal exposure has been associated with lower birth weight 26 and adverse neurodevelopmental effects. 27 , 28 , 29 …”
Section: Arsenic Sources and Toxicitymentioning
confidence: 99%