| Literature DB >> 27701120 |
Ksenia Blinova1, Jayna Stohlman2, Jose Vicente2,3,4, Dulciana Chan2, Lars Johannesen2, Maria P Hortigon-Vinagre5,6, Victor Zamora5,6, Godfrey Smith5,6, William J Crumb7, Li Pang8, Beverly Lyn-Cook8, James Ross9, Mathew Brock9, Stacie Chvatal9, Daniel Millard9, Loriano Galeotti2, Norman Stockbridge3, David G Strauss1,10.
Abstract
Induced pluripotent stem cell-derived cardiomyocytes (iPSC-CM) hold promise for assessment of drug-induced arrhythmias and are being considered for use under the comprehensive in vitro proarrhythmia assay (CiPA). We studied the effects of 26 drugs and 3 drug combinations on 2 commercially available iPSC-CM types using high-throughput voltage-sensitive dye and microelectrode-array assays being studied for the CiPA initiative and compared the results with clinical QT prolongation and torsade de pointes (TdP) risk. Concentration-dependent analysis comparing iPSC-CMs to clinical trial results demonstrated good correlation between drug-induced rate-corrected action potential duration and field potential duration (APDc and FPDc) prolongation and clinical trial QTc prolongation. Of 20 drugs studied that exhibit clinical QTc prolongation, 17 caused APDc prolongation (16 in Cor.4U and 13 in iCell cardiomyocytes) and 16 caused FPDc prolongation (16 in Cor.4U and 10 in iCell cardiomyocytes). Of 14 drugs that cause TdP, arrhythmias occurred with 10 drugs. Lack of arrhythmic beating in iPSC-CMs for the four remaining drugs could be due to differences in relative levels of expression of individual ion channels. iPSC-CMs responded consistently to human ether-a-go-go potassium channel blocking drugs (APD prolongation and arrhythmias) and calcium channel blocking drugs (APD shortening and prevention of arrhythmias), with a more variable response to late sodium current blocking drugs. Current results confirm the potential of iPSC-CMs for proarrhythmia prediction under CiPA, where iPSC-CM results would serve as a check to ion channel and in silico modeling prediction of proarrhythmic risk. A multi-site validation study is warranted. Published by Oxford University Press on behalf of the Society of Toxicology 2016. This work is written by US Government employees and is in the public domain in the US.Entities:
Keywords: CiPA; Cor.4U.; MEA; VSD; iCell; iPSC-CM
Mesh:
Year: 2016 PMID: 27701120 PMCID: PMC6093617 DOI: 10.1093/toxsci/kfw200
Source DB: PubMed Journal: Toxicol Sci ISSN: 1096-0929 Impact factor: 4.849