代谢综合征心房心律失常的结构基础

Shaleka Agrawal, G. Ramlugun, Kevin Jamart, James Kennelly, Jesse L. Ashton, G. Sands, M. Zarzoso, Jichao Zhao
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引用次数: 0

摘要

代谢综合征(MetS)的各个组成部分与心房颤动(AF)相关,但作为一个整体,AF易感性增加的确切机制仍不清楚。本研究确定了兔子代谢代谢的肥胖饮食模型中的关键结构底物。分别取材于met和对照组的兔心房(N=3),在小麦胚芽凝集素(WGA)中孵育,标记细胞膜和胶原。用共聚焦显微镜对组织成像。使用强大的机器学习架构V-net对胶原蛋白和细胞膜进行分割。通过计算每个分割图像中胶原总像元与心房组织总像元的比率来量化纤维化。通过测量单个细胞直径计算细胞肥大测量值。我们发现心房扩张,胶原蛋白增加,细胞肥大和轴小管减少。这些是确定的心律失常表型,可能导致房颤易感性增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Structural Basis of Atrial Arrhythmogenesis in Metabolic Syndrome
Individual components of metabolic syndrome (MetS) have been correlated with atrial fibrillation (AF), but as a whole, the exact mechanism underlying the increased susceptibility of AF still remains unclear. This study identifies key structural substrates in a robust obesogenic dietary model of MetS in the rabbits. The rabbit atria from both MetS and controls (N=3 each) were processed and incubated in wheat germ agglutinin (WGA) to label cell membranes and collagen. Confocal microscopy was used to image the tissue. The collagen and cell membranes were segmented using a robust machine learning architecture, V-net. Quantification of fibrosis was done by calculating the ratio of total pixels of collagen to those of atrial tissue in each of the segmented images. Cell hypertrophy measurements were calculated by measuring means of individual cell diameters. We discovered atrial dilation, increased collagen, cell hypertrophy and reduction in axial-tubules in MetS atria. These are established arrhythmogenic phenotypes which might lead to increased AF susceptibility.
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