The code provided is a computational model designed to simulate the behavior of the hyperpolarization-activated cyclic nucleotide-gated channel (HCN or "I_h") found predominantly in sinoatrial (SA) node cells of the heart. These cells are critical for pacemaking activities, which self-initiate action potentials governing heart rhythm. The specific focus here is on modeling the ion channel dynamics via a Markovian framework, capturing the complexity of channel opening and closing rates under different voltage conditions.
c1
, c2
, o1
, o2
, o3
) to represent the transitions between closed and open channel states, facilitating a detailed representation of ion channel kinetics.alpha
, beta
, myu
, and lambda
describe the rate of transitions between these states. These parameters capture the activation and deactivation behavior of the channels in response to voltage changes.ko
, ki
, Nao
, Nai
), reflecting their physiological values crucial for maintaining ionic gradients and electrophysiological properties of SA node cells.CFNa
and CFK
represent the driving forces for Na+ and K+, determined by relative ion concentrations and membrane potential. This factor is essential for accurately modeling ionic currents driven by channel activity.ihNa
) and K+ (ihK
) currents to the overall hyperpolarization-activated current (ih
) in SA node cells. This is fundamental for understanding how these channels influence heart rate.The code encapsulates a detailed biophysical representation of ion channel kinetics within sinoatrial pacemaker cells, leveraging known properties of HCN channels to simulate their voltage-dependent behavior and its impact on cardiac rhythmogenesis. This model serves as a tool for exploring the functional properties of HCN channels under varying conditions, thereby providing insights into their role in cardiac physiology.