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Gender Difference in Lithium-Induced Sodium Current Dysregulation and Ventricular Arrhythmogenesis in Right Ventricular Outflow Tract Cardiomyocytes

Lithium intoxication induces Brugada-pattern ECG, ventricular arrhythmia, and sudden death with the predominant preference for the male over the female gender. This study investigated the mechanisms of gender difference in lithium-induced arrhythmogenesis. The ECG parameters were recorded in male an...

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Autores principales: Liu, Ching-Han, Chen, Yao-Chang, Lu, Yen-Yu, Lin, Yung-Kuo, Higa, Satoshi, Chen, Shih-Ann, Chen, Yi-Jen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687181/
https://www.ncbi.nlm.nih.gov/pubmed/36359250
http://dx.doi.org/10.3390/biomedicines10112727
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author Liu, Ching-Han
Chen, Yao-Chang
Lu, Yen-Yu
Lin, Yung-Kuo
Higa, Satoshi
Chen, Shih-Ann
Chen, Yi-Jen
author_facet Liu, Ching-Han
Chen, Yao-Chang
Lu, Yen-Yu
Lin, Yung-Kuo
Higa, Satoshi
Chen, Shih-Ann
Chen, Yi-Jen
author_sort Liu, Ching-Han
collection PubMed
description Lithium intoxication induces Brugada-pattern ECG, ventricular arrhythmia, and sudden death with the predominant preference for the male over the female gender. This study investigated the mechanisms of gender difference in lithium-induced arrhythmogenesis. The ECG parameters were recorded in male and female rabbits before and after the intravenous administration of lithium chloride (LiCl) (1, 3, 10 mmol/kg). Patch clamps were used to study the sodium current (I(Na)) and late sodium current (I(Na-late)) in the isolated single male and female right ventricular outflow tract (RVOT) cardiomyocytes before and after LiCl. Male rabbits (n = 9) were more prone to developing lithium-induced Brugada-pattern ECG changes (incomplete right bundle branch block, ST elevation and QRS widening) with fatal arrhythmia (66.7% vs. 0%, p = 0.002) than in female (n = 7) rabbits at 10 mmol/kg (but not 1 or 3 mmol/kg). Compared to those in the female RVOT cardiomyocytes, LiCl (100 μM) reduced I(Na) to a greater extent and increased I(Na-late) in the male RVOT cardiomyocytes. Moreover, in the presence of ranolazine (the I(Na-late) inhibitor, 3.6 mg/kg iv loading, followed by a second iv bolus 6.0 mg/kg administered 30 min later, n = 5), LiCl (10 mmol/kg) did not induce Brugada-pattern ECG changes (p < 0.005). The male gender is much predisposed to lithium-induced Brugada-pattern ECG changes with a greater impact on I(Na) and I(Na-late) in RVOT cardiomyocytes. Targeting I(Na-late) may be a potential therapeutic strategy for Brugada syndrome-related ventricular tachyarrhythmia.
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spelling pubmed-96871812022-11-25 Gender Difference in Lithium-Induced Sodium Current Dysregulation and Ventricular Arrhythmogenesis in Right Ventricular Outflow Tract Cardiomyocytes Liu, Ching-Han Chen, Yao-Chang Lu, Yen-Yu Lin, Yung-Kuo Higa, Satoshi Chen, Shih-Ann Chen, Yi-Jen Biomedicines Article Lithium intoxication induces Brugada-pattern ECG, ventricular arrhythmia, and sudden death with the predominant preference for the male over the female gender. This study investigated the mechanisms of gender difference in lithium-induced arrhythmogenesis. The ECG parameters were recorded in male and female rabbits before and after the intravenous administration of lithium chloride (LiCl) (1, 3, 10 mmol/kg). Patch clamps were used to study the sodium current (I(Na)) and late sodium current (I(Na-late)) in the isolated single male and female right ventricular outflow tract (RVOT) cardiomyocytes before and after LiCl. Male rabbits (n = 9) were more prone to developing lithium-induced Brugada-pattern ECG changes (incomplete right bundle branch block, ST elevation and QRS widening) with fatal arrhythmia (66.7% vs. 0%, p = 0.002) than in female (n = 7) rabbits at 10 mmol/kg (but not 1 or 3 mmol/kg). Compared to those in the female RVOT cardiomyocytes, LiCl (100 μM) reduced I(Na) to a greater extent and increased I(Na-late) in the male RVOT cardiomyocytes. Moreover, in the presence of ranolazine (the I(Na-late) inhibitor, 3.6 mg/kg iv loading, followed by a second iv bolus 6.0 mg/kg administered 30 min later, n = 5), LiCl (10 mmol/kg) did not induce Brugada-pattern ECG changes (p < 0.005). The male gender is much predisposed to lithium-induced Brugada-pattern ECG changes with a greater impact on I(Na) and I(Na-late) in RVOT cardiomyocytes. Targeting I(Na-late) may be a potential therapeutic strategy for Brugada syndrome-related ventricular tachyarrhythmia. MDPI 2022-10-28 /pmc/articles/PMC9687181/ /pubmed/36359250 http://dx.doi.org/10.3390/biomedicines10112727 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Liu, Ching-Han
Chen, Yao-Chang
Lu, Yen-Yu
Lin, Yung-Kuo
Higa, Satoshi
Chen, Shih-Ann
Chen, Yi-Jen
Gender Difference in Lithium-Induced Sodium Current Dysregulation and Ventricular Arrhythmogenesis in Right Ventricular Outflow Tract Cardiomyocytes
title Gender Difference in Lithium-Induced Sodium Current Dysregulation and Ventricular Arrhythmogenesis in Right Ventricular Outflow Tract Cardiomyocytes
title_full Gender Difference in Lithium-Induced Sodium Current Dysregulation and Ventricular Arrhythmogenesis in Right Ventricular Outflow Tract Cardiomyocytes
title_fullStr Gender Difference in Lithium-Induced Sodium Current Dysregulation and Ventricular Arrhythmogenesis in Right Ventricular Outflow Tract Cardiomyocytes
title_full_unstemmed Gender Difference in Lithium-Induced Sodium Current Dysregulation and Ventricular Arrhythmogenesis in Right Ventricular Outflow Tract Cardiomyocytes
title_short Gender Difference in Lithium-Induced Sodium Current Dysregulation and Ventricular Arrhythmogenesis in Right Ventricular Outflow Tract Cardiomyocytes
title_sort gender difference in lithium-induced sodium current dysregulation and ventricular arrhythmogenesis in right ventricular outflow tract cardiomyocytes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9687181/
https://www.ncbi.nlm.nih.gov/pubmed/36359250
http://dx.doi.org/10.3390/biomedicines10112727
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