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Automated Patch-Clamp and Induced Pluripotent Stem Cell-Derived Cardiomyocytes: A Synergistic Approach in the Study of Brugada Syndrome

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Publisher

MDPI
DOI: 10.3390/ijms24076687

Keywords

Brugada syndrome (BrS); BrS experimental model; automated patch-clamp; human-induced pluripotent stem cells; hiPSCs; hiPSCs-CM; patient-derived cardiomyocytes; personalized medicine

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The development of high-throughput automated patch-clamp technology is a recent breakthrough in Brugada syndrome research. This technology, combined with the use of patient-derived cardiomyocytes, has greatly improved our understanding of the underlying mechanisms of this condition and led to the development of more effective treatments for cardiovascular diseases.
The development of high-throughput automated patch-clamp technology is a recent breakthrough in the field of Brugada syndrome research. Brugada syndrome is a heart disorder marked by abnormal electrocardiographic readings and an elevated risk of sudden cardiac death due to arrhythmias. Various experimental models, developed either in animals, cell lines, human tissue or computational simulation, play a crucial role in advancing our understanding of this condition, and developing effective treatments. In the perspective of the pathophysiological role of ion channels and their pharmacology, automated patch-clamp involves a robotic system that enables the simultaneous recording of electrical activity from multiple single cells at once, greatly improving the speed and efficiency of data collection. By combining this approach with the use of patient-derived cardiomyocytes, researchers are gaining a more comprehensive view of the underlying mechanisms of heart disease. This has led to the development of more effective treatments for those affected by cardiovascular conditions.

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