Suppr超能文献

先天性心脏传导阻滞患儿母亲的血清和免疫球蛋白G在大鼠心脏模型中可诱发传导异常并抑制L型钙通道。

Serum and immunoglobulin G from the mother of a child with congenital heart block induce conduction abnormalities and inhibit L-type calcium channels in a rat heart model.

作者信息

Boutjdir M, Chen L, Zhang Z H, Tseng C E, El-Sherif N, Buyon J P

机构信息

Division of Cardiology, Veterans Administration Medical Center and Center for Cardiovascular and Muscular Research, State University of New York, Brooklyn 11209, USA.

出版信息

Pediatr Res. 1998 Jul;44(1):11-9. doi: 10.1203/00006450-199807000-00002.

Abstract

Although a strong clinical association exists between congenital heart block (CHB) and an immune response to SSA/Ro and SSB/La proteins, a causative role of these antibodies in the pathogenesis is just emerging. In a preliminary report, we have demonstrated that IgG fractions isolated from the sera of mothers whose children have CHB are arrhythmogenic in the human fetal heart. To more precisely define the arrhythmogenic effect of anti-SSA/Ro-SSB/La antibodies, we used the readily available rat heart model to record: 1) ECGs from Langendorff beating hearts; 2) action potentials from atrioventricular (AV) nodal preparations; 3) L-type Ca currents, I(Ca) at the whole-cell and single channel levels; and 4) other currents such as the transient outward K+ current, I(to), the inward rectifier K+ current, I(K1), and the Na+ current, I(Na). Perfusion of hearts with purified IgG (800 microg/mL), isolated from the serum of a mother with SSA/Ro and SSB/La antibodies whose child had CHB, resulted in bradycardia associated with 2:1 AV block. Simultaneous action potentials were recorded from dissected atrial and AV nodal areas of the rat heart. Superfusion of these preparations with the same mother's IgG fraction resulted in 2:1 AV block followed by complete inhibition of AV nodal action potential. Because AV nodal electrogenesis is largely dependent on I(Ca), the effect of these antibodies on I(Ca) was subsequently determined. Superfusion of myocytes with whole serum or purified IgG (80 microg/mL) from the same mother consistently inhibited whole cell I(Ca), ensemble average Ba2+ currents (I(Ba)) and open state probability, p(o), without affecting the channel conductance. IgG had no significant effect on I(to), I(K1), or I(Na). Whole sera and IgG fractions from a healthy mother with no detectable anti-SSA/Ro or SSB/La antibodies did not inhibit I(Ca) or I(Ba). These results demonstrate that IgG containing anti-SSA/Ro and -SSB/La antibodies induces complete AV block in beating hearts and in multicellular preparations, thus implicating a preferential interaction of these autoantibodies with Ca channels and/or associated regulatory proteins. This is consistent with the observed inhibition of Ca channels that may be a critical factor contributing to the pathogenesis of CHB.

摘要

尽管先天性心脏传导阻滞(CHB)与针对SSA/Ro和SSB/La蛋白的免疫反应之间存在很强的临床关联,但这些抗体在发病机制中的致病作用才刚刚显现。在一份初步报告中,我们已经证明,从患有CHB孩子的母亲血清中分离出的IgG组分在人类胎儿心脏中具有致心律失常作用。为了更精确地确定抗SSA/Ro - SSB/La抗体的致心律失常作用,我们使用了易于获得的大鼠心脏模型来记录:1)Langendorff跳动心脏的心电图;2)房室(AV)结标本的动作电位;3)全细胞和单通道水平的L型钙电流I(Ca);以及4)其他电流,如瞬时外向钾电流I(to)、内向整流钾电流I(K1)和钠电流I(Na)。用从一名患有CHB孩子的、具有SSA/Ro和SSB/La抗体的母亲血清中分离出的纯化IgG(800微克/毫升)灌注心脏,导致心动过缓并伴有2:1房室传导阻滞。同时从大鼠心脏解剖的心房和房室结区域记录动作电位。用同一位母亲的IgG组分对这些标本进行灌流,导致2:1房室传导阻滞,随后房室结动作电位完全被抑制。由于房室结电活动在很大程度上依赖于I(Ca),随后确定了这些抗体对I(Ca)的影响。用来自同一位母亲的全血清或纯化IgG(80微克/毫升)对心肌细胞进行灌流,持续抑制全细胞I(Ca)、总体平均Ba2+电流(I(Ba))和开放状态概率p(o),而不影响通道电导。IgG对I(to)、I(K1)或I(Na)没有显著影响。来自一名未检测到抗SSA/Ro或SSB/La抗体的健康母亲的全血清和IgG组分不抑制I(Ca)或I(Ba)。这些结果表明,含有抗SSA/Ro和 - SSB/La抗体的IgG在跳动的心脏和多细胞标本中诱导完全性房室传导阻滞,从而提示这些自身抗体与钙通道和/或相关调节蛋白存在优先相互作用。这与观察到的钙通道抑制现象一致,而钙通道抑制可能是导致CHB发病机制的一个关键因素。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验