Alterations of Myocardial Mitochondrial Morphology and Function in a Canine Model of Premature Ventricular Contractions-Induced Cardiomyopathy

• Published in: Frontiers in bioscience (Landmark. Print) Vol. 29; no. 5; p. 200
• Main Authors: Liu, Tao, Yang, Manqi, Cui, Bo, Ju, Hao, Wu, Jinchun, Ren, Zongli, Cao, Sheng, Yan, Min, Zhang, Fan, Liu, Zheyu, He, Shuijing, Zhang, Jiajun, Hiram, Roddy, Xiong, Feng, Cheng, Mian, Wu, Gang
• Format: Journal Article
• Language: English
• Published: Singapore IMR Press 22.05.2024
• Subjects: Adenosine Triphosphate - metabolism; Animals; Calcium - metabolism; Cardiomyopathies - etiology; Cardiomyopathies - metabolism; Cardiomyopathies - pathology; Cardiomyopathies - physiopathology; cardiomyopathy; coupling interval; Disease Models, Animal; Dogs; Echocardiography; Male; Membrane Potential, Mitochondrial; mitochondria; Mitochondria, Heart - metabolism; Mitochondria, Heart - pathology; Mitochondria, Heart - ultrastructure; myocardial fibrosis; premature ventricular contractions; Reactive Oxygen Species - metabolism; Ventricular Premature Complexes - metabolism; Ventricular Premature Complexes - physiopathology; coupling interval; cardiomyopathy; mitochondria; myocardial fibrosis; premature ventricular contractions
• ISSN: 2768-6701; 2768-6698
• DOI: 10.31083/j.fbl2905200

Changes in myocardial mitochondrial morphology and function in premature ventricular contractions (PVCs)-induced cardiomyopathy (PVCCM) remain poorly studied. Here, we investigated the effects of PVCs with different coupling intervals (CIs) on myocardial mitochondrial remodelling in a canine model of PVCCM. Twenty-one beagles underwent pacemaker implantation and were randomised into the sham (n = 7), short-coupled PVCs (SCP, n = 7), and long-coupled PVCs (LCP, n = 7) groups. Right ventricular (RV) apical bigeminy was produced for 12-week to induce PVCCM in the SCP (CI, 250 ms) and LCP (CI, 350 ms) groups. Echocardiography was performed at baseline and biweekly thereafter to evaluate cardiac function. Masson's trichrome staining measured ventricular interstitial fibrosis. The ultrastructural morphology of the myocardial mitochondria was analysed using transmission electron microscopy. Mitochondrial Ca2+ concentration, reactive oxygen species (ROS) levels, adenosine triphosphate (ATP) content, membrane potential, and electron transport chain (ETC) complex activity were measured to assess myocardial mitochondrial function. Twelve-week-PVCs led to left ventricular (LV) enlargement with systolic dysfunction, disrupted mitochondrial morphology, increased mitochondrial Ca2+ concentration and ROS levels, decreased mitochondrial ATP content and membrane potential, and impaired ETC complex activity in both the SCP and LCP groups (all < 0.01 the sham group). Ventricular fibrosis was observed only in canines with LCP. Worse cardiac function and more pronounced abnormalities in mitochondrial morphology and function were observed in the LCP group than to the SCP group (all < 0.05). We demonstrated myocardial mitochondrial abnormalities in dogs with PVCCM, characterised by abnormal mitochondrial morphology, mitochondrial Ca2+ overload, oxidative stress, and impaired mitochondrial energy metabolism. Compared to SCP, long-term LCP exposure resulted in more severe mitochondrial remodelling and cardiac dysfunction in dogs.