scholarly journals Eleutheroside B, a selective late sodium current inhibitor, suppresses atrial fibrillation induced by sea anemone toxin II in rabbit hearts

Author(s):  
Pei-pei Zhang ◽  
Zhao-fu Guo ◽  
Pei-hua Zhang ◽  
Zhi-pei Liu ◽  
Lv Song ◽  
...  
2020 ◽  
Vol 76 (4) ◽  
pp. 437-444
Author(s):  
Yanpeng Chu ◽  
Qiaomei Yang ◽  
Lu Ren ◽  
Shandong Yu ◽  
Zhipei Liu ◽  
...  

PLoS ONE ◽  
2015 ◽  
Vol 10 (6) ◽  
pp. e0131432 ◽  
Author(s):  
Claire Poulet ◽  
Erich Wettwer ◽  
Morten Grunnet ◽  
Thomas Jespersen ◽  
Larissa Fabritz ◽  
...  

Circulation ◽  
2020 ◽  
Vol 142 (Suppl_3) ◽  
Author(s):  
Liang HONG ◽  
Olivia T Ly ◽  
Hanna Chen ◽  
Arvind Sridhar ◽  
Meihong Zhang ◽  
...  

Introduction: Gain-of-function mutations in SCN5A, which encodes the cardiac sodium channel, have been linked with familial atrial fibrillation (AF). However, the mechanistic link between the late sodium current (I Na,L ) and triggered arrhythmia remains unclear. Hypothesis: To characterize the electrophysiological (EP) phenotype of gain-of-function AF-linked SCN5A mutations, elucidate the underlying cellular mechanisms using patient-specific and gene-corrected (GC) induced pluripotent stem cell-derived atrial cardiomyocytes (iPSC-aCMs). Methods: We generated iPSC-aCMs from two families carrying SCN5A mutations (E428K and N470K) and control subjects. Whole-cell patch clamp and multi-electrode arrays were recorded to assess the EP phenotypes of the atrial iPSC-CMs. We corrected the E428K iPSC-aCMs using CRISPR/Cas9 gene editing approach (isogenic control). Results: The SCN5A mutation lines displayed abnormal EP properties including increased beating frequency and irregularity with triggered beats characteristic of AF ( Fig. 1 ). E428K iPSC-aCMs displayed spontaneous arrhythmogenic activity with beat-to-beat irregularity ( Fig. 1 A-D ) with the prolonged APD ( Fig. 1 E-H ) associated with enhanced I Na,L ( Fig. 1 I-L ). In contrast, expression of SCN5A -E428K in heterologous expression system failed to show enhanced I Na,L . The gene-corrected E428K iPSC-aCMs normalized the aberrant EP phenotype. Gene expression profiling revealed differential expression of calcium and potassium channel homeostasis and nitric oxide mediated signal transduction which could result in EP remodeling of atrial CMs. Conclusions: Patient-specific and gene-corrected iPSC-aCMs exhibited striking ex-vivo EP phenotype of an AF-causing SCN5A gain-of-function mutation that produced minimal changes in-vitro . We established a mechanistic link between enhanced I Na,L , ion channel remodeling and nitric oxide signaling pathways, and triggered AF.


2019 ◽  
Vol 125 (Suppl_1) ◽  
Author(s):  
Ambili Menon ◽  
Brandon Chalzan ◽  
Liang Hong ◽  
Arvind sridhar ◽  
Meihong Zhang ◽  
...  

2015 ◽  
Vol 65 (10) ◽  
pp. A392
Author(s):  
Richard L. Verrier ◽  
Juliana S. Carneiro ◽  
Afonso Alves Bento ◽  
Danilo Bacic ◽  
Bruce Nearing ◽  
...  

2019 ◽  
Vol 857 ◽  
pp. 172444 ◽  
Author(s):  
Xuexin Jin ◽  
Yuan Jiang ◽  
Genlong Xue ◽  
Yin Yuan ◽  
Haixia Zhu ◽  
...  

Heart Rhythm ◽  
2012 ◽  
Vol 9 (11) ◽  
pp. 1911
Author(s):  
E. Savio Galimberti ◽  
C.G. Vanoye ◽  
T. Yang ◽  
T.C. Atack ◽  
R. Muhammad ◽  
...  

2020 ◽  
Vol 41 (Supplement_2) ◽  
Author(s):  
I Del Canto Serrano ◽  
L Gomez-Cid ◽  
A.S De La Nava ◽  
M.S Guillem ◽  
M.E Fernandez-Santos ◽  
...  

Abstract Background The cardiac late sodium current (INaL) has been increasingly implicated in the initiation of atrial fibrillation (AF). In fact, it has been reported that the augmentation of INaL in pathophysiological conditions prolongs repolarization and facilitates the appearance of afterdepolarizations, which can act as triggers of arrhythmic activity. Eleclazine is a novel selective inhibitor of INaL and is undergoing clinical testing for the treatment of cardiac arrhythmias. Purpose The aim of this study was to investigate the effects of eleclazine on spectral characteristics of atrial fibrillation in cultured atrial myocyte monolayer in order to assess whether this inhibitor could protect against cardiac arrhythmias. Methods Confluent HL-1 murine atrial myocyte monolayer with spontaneous fibrillatory activity was cultured in 1.5 cm diameter petri dishes (n=10). A high-resolution optical mapping system was used to record fibrillatory activity under basal conditions (without drug), and under eleclazine at increasing concentrations (1, 3 and 5 μM). Power spectra of optical signals were estimated by using Welch periodogram and dominant frequency (frequency with the largest peak in the spectrum between 0.05 and 30 Hz) was determined. The incidence of spontaneous defibrillation was analyzed under control and drug conditions. An ANOVA and a chi-squared test were used. Significance was reached when p<0.05. Results Eleclazine at 1, 3 and 5 μM significantly decreased dominant frequency with respect to basal conditions (basal: 4.74±1.31 Hz; 1μM: 3.59±1.17 Hz, p<0.001; 3μM: 3.19±0.64 Hz, p<0.01; 5μM: 2.58±0.40 Hz, p<0.01). The magnitude of drug-induced decrease in AF activation frequency was enhanced by increasing concentrations (1μM: 27%, 3μM: 42%; 5μM: 46%; p<0.05). After the analysis of optical signals, we observed that the incidence of spontaneous defibrillation in atrial monolayers was significantly greater under eleclazine 5μM action than under control conditions (chi-square=5.00, p=0.025). In fact, under the action of eleclazine 5μM, fibrillatory activity was suppressed in 4 of the 10 monolayers, phenomenon that did not occur in any case of control situation. Conclusions Selective late INa inhibition with eleclazine reduced dominant frequency of atrial fibrillation and facilitates the termination of arrhythmia in cultured atrial myocyte monolayer. Funding Acknowledgement Type of funding source: Public grant(s) – National budget only. Main funding source(s): Instituto de Salud Carlos III, Ministerio de Innovaciόn y Ciencia, Spain; Generalitat Valenciana, Spain


2016 ◽  
Vol 67 (13) ◽  
pp. 751
Author(s):  
Henrique Fuller ◽  
Fernanda Justo ◽  
Bruce Nearing ◽  
Sridharan Rajamani ◽  
Luiz Belardinelli ◽  
...  

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