alternan and Brugada-Syndrome

alternan has been researched along with Brugada-Syndrome* in 2 studies

Other Studies

2 other study(ies) available for alternan and Brugada-Syndrome

ArticleYear
Atrial SERCA2a Overexpression Has No Affect on Cardiac Alternans but Promotes Arrhythmogenic SR Ca2+ Triggers.
    PloS one, 2015, Volume: 10, Issue:9

    Atrial fibrillation (AF) is the most common arrhythmia in humans, yet; treatment has remained sub-optimal due to poor understanding of the underlying mechanisms. Cardiac alternans precede AF episodes, suggesting an important arrhythmia substrate. Recently, we demonstrated ventricular SERCA2a overexpression suppresses cardiac alternans and arrhythmias. Therefore, we hypothesized that atrial SERCA2a overexpression will decrease cardiac alternans and arrhythmias.. Adult rat isolated atrial myocytes where divided into three treatment groups 1) Control, 2) SERCA2a overexpression (Ad.SERCA2a) and 3) SERCA2a inhibition (Thapsigargin, 1μm). Intracellular Ca2+ was measured using Indo-1AM and Ca2+ alternans (Ca-ALT) was induced with a standard ramp pacing protocol.. As predicted, SR Ca2+ reuptake was enhanced with SERCA2a overexpression (p< 0.05) and reduced with SERCA2a inhibition (p<0.05). Surprisingly, there was no difference in susceptibility to Ca-ALT with either SERCA2a overexpression or inhibition when compared to controls (p = 0.73). In contrast, SERCA2a overexpression resulted in increased premature SR Ca2+ (SCR) release compared to control myocytes (28% and 0%, p < 0.05) and concomitant increase in SR Ca2+ load (p<0.05). Based on these observations we tested in-vivo atrial arrhythmia inducibility in control and Ad.SERCA2a animals using an esophageal atrial burst pacing protocol. There were no inducible atrial arrhythmias in Ad.GFP (n = 4) animals though 20% of Ad.SERCA2a (n = 5) animals had inducible atrial arrhythmias (p = 0.20).. Our findings suggest that unlike the ventricle, SERCA2a is not a key regulator of cardiac alternans in the atrium. Importantly, SERCA2a overexpression in atrial myocytes can increase SCR, which may be arrhythmogenic.

    Topics: Animals; Arrhythmias, Cardiac; Atrial Fibrillation; Brugada Syndrome; Calcium; Cardiac Conduction System Disease; Gene Expression Regulation; Glucans; Heart Atria; Heart Conduction System; Humans; Myocytes, Cardiac; Patch-Clamp Techniques; Rats; Sarcoplasmic Reticulum Calcium-Transporting ATPases; Thapsigargin

2015
POSTEXTRASYSTOLIC ALTERNANS OF THE U WAVE DU TO HYPOKALEMIA.
    American heart journal, 1964, Volume: 68

    Topics: Arrhythmias, Cardiac; Brugada Syndrome; Cardiac Complexes, Premature; Cardiac Conduction System Disease; Electrocardiography; Glucans; Heart Conduction System; Humans; Hypokalemia

1964