Mechanistic insight into the functional role of human sinoatrial node conduction pathways and pacemaker compartments heterogeneity: A computer model analysis

• Published in: PLoS computational biology 2023-12, Vol.19 (12), p.e1011708-e1011708
• Main Authors: Zhao, Jichao, Sharma, Roshan, Kalyanasundaram, Anuradha, Kennelly, James, Bai, Jieyun, Li, Ning, Panfilov, Alexander, Fedorov, Vadim V
• Format: Article
• Language: English
• Subjects: Adenosine; Adenosine A1 receptors; Analysis; Arrhythmia; Atria; Automation; Biology and Life Sciences; Blood vessels; Compartments; Computer and Information Sciences; Computer simulation; Computer-generated environments; Conduction; Electrical insulation; Engineering and Technology; Fibrosis; Heart; Heterogeneity; Histology; Ion channels; Mapping; Mathematical models; Medicine and Health Sciences; Pacemakers; Physical Sciences; Physiology; Receptors; Rhythm; Robustness; Sinoatrial node; Structure-function relationships
• ISSN: 1553-7358; 1553-734X; 1553-7358
• DOI: 10.1371/journal.pcbi.1011708

The sinoatrial node (SAN), the primary pacemaker of the heart, is responsible for the initiation and robust regulation of sinus rhythm. 3D mapping studies of the ex-vivo human heart suggested that the robust regulation of sinus rhythm relies on specialized fibrotically-insulated pacemaker compartments (head, center and tail) with heterogeneous expressions of key ion channels and receptors. They also revealed up to five sinoatrial conduction pathways (SACPs), which electrically connect the SAN with neighboring right atrium (RA). To elucidate the role of these structural-molecular factors in the functional robustness of human SAN, we developed comprehensive biophysical computer models of the SAN based on 3D structural, functional and molecular mapping of ex-vivo human hearts. Our key finding is that the electrical insulation of the SAN except SACPs, the heterogeneous expression of If, INa currents and adenosine A1 receptors (A1R) across SAN pacemaker-conduction compartments are required to experimentally reproduce observed SAN activation patterns and important phenomena such as shifts of the leading pacemaker and preferential SACP. In particular, we found that the insulating border between the SAN and RA, is required for robust SAN function and protection from SAN arrest during adenosine challenge. The heterogeneity in the expression of A1R within the human SAN compartments underlies the direction of pacemaker shift and preferential SACPs in the presence of adenosine. Alterations of INa current and fibrotic remodelling in SACPs can significantly modulate SAN conduction and shift the preferential SACP/exit from SAN. Finally, we show that disease-induced fibrotic remodeling, INa suppression or increased adenosine make the human SAN vulnerable to pacing-induced exit blocks and reentrant arrhythmia. In summary, our computer model recapitulates the structural and functional features of the human SAN and can be a valuable tool for investigating mechanisms of SAN automaticity and conduction as well as SAN arrhythmia mechanisms under different pathophysiological conditions.