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A low voltage activated Ca(2+) current found in a subset of human ventricular myocytes
Low voltage activated (I(Ca-LVA)) calcium currents including Cav1.3 and T-type calcium current (I(Ca-T)) have not been reported in adult human left ventricular myocytes (HLVMs). We tried to examine their existence and possible correlation with etiology and patient characteristics in a big number of...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7515576/ https://www.ncbi.nlm.nih.gov/pubmed/32684070 http://dx.doi.org/10.1080/19336950.2020.1794420 |
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author | Zhang, Xin Li, Yijia Zhang, Xiaoying Piacentino, Valentino Harris, David M. Berretta, Remus Margulies, Kenneth B. Houser, Steven R. Chen, Xiongwen |
author_facet | Zhang, Xin Li, Yijia Zhang, Xiaoying Piacentino, Valentino Harris, David M. Berretta, Remus Margulies, Kenneth B. Houser, Steven R. Chen, Xiongwen |
author_sort | Zhang, Xin |
collection | PubMed |
description | Low voltage activated (I(Ca-LVA)) calcium currents including Cav1.3 and T-type calcium current (I(Ca-T)) have not been reported in adult human left ventricular myocytes (HLVMs). We tried to examine their existence and possible correlation with etiology and patient characteristics in a big number of human LVMs isolated from explanted terminally failing (F) hearts, failing hearts with left ventricular assist device (F-LVAD) and nonfailing (NF) human hearts. LVA (I(Ca-LVA)) was determined by subtracting L-type Ca(2+) current (I(Ca-L)) recorded with the holding potential of −50 mV from total Ca(2+) current recorded with the holding potential of −90 mV or −70 mV. I(Ca- LVA) was further tested with its sensitivity to 100 µM CdCl(2) and tetrodotoxin. Three HLVMs (3 of 137 FHLVMs) from 2 (N = 30 hearts) failing human hearts, of which one was idiopathic and the other was due to primary pulmonary hypertension, were found with I(Ca-LVA). I(Ca-LVA) in one FHLVM was not sensitive to 100 µM CdCl(2) while I(Ca-LVA) in another two FHLVMs was not sensitive to tetrodotoxin. It peaked at the voltage of −40~-20 mV and had a time-dependent decay faster than I(Ca-L) but slower than sodium current (I(Na)). I(Ca-LVA) was not found in any HLVMs from NF (75 HLVMs from 17 hearts) or F-LVAD hearts (82 HLVMs from 18 hearts) but a statistically significant correlation could not be established. In conclusion, I(Ca-LVA) was detected in some HLVMs of a small portion of human hearts that happened to be nonischemic failing hearts. |
format | Online Article Text |
id | pubmed-7515576 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-75155762020-10-01 A low voltage activated Ca(2+) current found in a subset of human ventricular myocytes Zhang, Xin Li, Yijia Zhang, Xiaoying Piacentino, Valentino Harris, David M. Berretta, Remus Margulies, Kenneth B. Houser, Steven R. Chen, Xiongwen Channels (Austin) Research Paper Low voltage activated (I(Ca-LVA)) calcium currents including Cav1.3 and T-type calcium current (I(Ca-T)) have not been reported in adult human left ventricular myocytes (HLVMs). We tried to examine their existence and possible correlation with etiology and patient characteristics in a big number of human LVMs isolated from explanted terminally failing (F) hearts, failing hearts with left ventricular assist device (F-LVAD) and nonfailing (NF) human hearts. LVA (I(Ca-LVA)) was determined by subtracting L-type Ca(2+) current (I(Ca-L)) recorded with the holding potential of −50 mV from total Ca(2+) current recorded with the holding potential of −90 mV or −70 mV. I(Ca- LVA) was further tested with its sensitivity to 100 µM CdCl(2) and tetrodotoxin. Three HLVMs (3 of 137 FHLVMs) from 2 (N = 30 hearts) failing human hearts, of which one was idiopathic and the other was due to primary pulmonary hypertension, were found with I(Ca-LVA). I(Ca-LVA) in one FHLVM was not sensitive to 100 µM CdCl(2) while I(Ca-LVA) in another two FHLVMs was not sensitive to tetrodotoxin. It peaked at the voltage of −40~-20 mV and had a time-dependent decay faster than I(Ca-L) but slower than sodium current (I(Na)). I(Ca-LVA) was not found in any HLVMs from NF (75 HLVMs from 17 hearts) or F-LVAD hearts (82 HLVMs from 18 hearts) but a statistically significant correlation could not be established. In conclusion, I(Ca-LVA) was detected in some HLVMs of a small portion of human hearts that happened to be nonischemic failing hearts. Taylor & Francis 2020-07-20 /pmc/articles/PMC7515576/ /pubmed/32684070 http://dx.doi.org/10.1080/19336950.2020.1794420 Text en © 2020 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Paper Zhang, Xin Li, Yijia Zhang, Xiaoying Piacentino, Valentino Harris, David M. Berretta, Remus Margulies, Kenneth B. Houser, Steven R. Chen, Xiongwen A low voltage activated Ca(2+) current found in a subset of human ventricular myocytes |
title | A low voltage activated Ca(2+) current found in a subset of human ventricular myocytes |
title_full | A low voltage activated Ca(2+) current found in a subset of human ventricular myocytes |
title_fullStr | A low voltage activated Ca(2+) current found in a subset of human ventricular myocytes |
title_full_unstemmed | A low voltage activated Ca(2+) current found in a subset of human ventricular myocytes |
title_short | A low voltage activated Ca(2+) current found in a subset of human ventricular myocytes |
title_sort | low voltage activated ca(2+) current found in a subset of human ventricular myocytes |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7515576/ https://www.ncbi.nlm.nih.gov/pubmed/32684070 http://dx.doi.org/10.1080/19336950.2020.1794420 |
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