Researchers at NYU Langone Medical Center have developed the first large animal model of an inherited arrhythmic syndrome - an advance that will lead to a better understanding of the biologic mechanisms important in normal heart conduction and rhythm. The novel pig model points the way toward development of better treatments for inherited forms of life-threatening arrhythmias, which are a significant cause of sudden cardiac death.
The findings, published online today in the Journal of Clinical Investigation, shed light on what causes lethal arrhythmias in the face of abnormal cardiac sodium channels. The proper functioning of these channels is essential for maintaining normal conduction in the heart. Disease-causing mutations in cardiac ion channels, technically referred to as "channelopathies," can lead to progressive cardiac conduction disorders, atrial and ventricular arrhythmias, and sudden cardiac death.
"By developing a genetically engineered pig sodium channelopathy model, we are now able to examine the mechanisms responsible for lethal arrhythmias in a human-like heart and investigate new therapies aimed at reducing sudden cardiac death," said lead author David S. Park, MD, PhD, assistant professor, Leon H. Charney Division of Cardiology, Department of Medicine at NYU Langone.
Until now, researchers have primarily used cultured heart cells and mouse models to study cardiac arrhythmias. "But because of similarities of the pig heart to human hearts, research with the pig model will prove invaluable in gaining further insights into the mechanisms that underlie life-threatening arrhythmias," said Glenn I. Fishman, MD, the study's senior author, and Director of the Leon H. Charney Division of Cardiology at NYU Langone.
Both Drs. Fishman and Park envision a future where novel therapies, such as drugs that can enhance cardiac sodium channel expression or radiofrequency ablation procedures, can first be tested in the pig model before application to patients. "A better understanding of arrhythmia mechanisms should yield better therapies in the future," said Dr. Park.
Other NYU Langone researchers collaborating on this study include Marina Cerrone, MD, Gregory Morley, PhD, Carolina Vasquez, PhD, Steven Fowler, MD, Nian Liu, MD, Scott A. Bernstein, MD, Fang-Yu Liu, BS, Jie Zhang, MD, Silvia G. Priori, MD, PhD, and Larry Chintz, MD. Christopher S. Rogers, PhD, also contributed to this study and is an employee and shareholder of Exemplar Genetics.
About NYU Langone Medical Center
NYU Langone Medical Center, a world-class, patient-centered, integrated academic medical center, is one of the nation's premier centers for excellence in clinical care, biomedical research, and medical education. Located in the heart of Manhattan, NYU Langone is composed of four hospitals--Tisch Hospital, its flagship acute care facility; Rusk Rehabilitation; the Hospital for Joint Diseases, and the Medical Center's dedicated inpatient orthopaedic hospital--plus the NYU School of Medicine, which since 1841 has trained thousands of physicians and scientists who have helped to shape the course of medical history. The Medical Center's tri-fold mission to serve, teach, and discover is achieved 365 days a year through the seamless integration of a culture devoted to excellence in patient care, education, and research. For more information, go to http://www.