Ion channels play crucial roles in cardiac function, regulating the flow of ions across cell membranes in response to various stimuli. These proteins exhibit selective permeability to specific ions such as Na+, K+, Ca++ and Cl− and their gating mechanisms can be voltage-dependent, ligand-dependent, or mechano-sensitive. Sodium channels, for example, are essential for cardiac action potentials and are implicated in various heart pathologies. Mutations in these channels can lead to situations like long QT syndrome and Brugada syndrome. Calcium channels are vital for excitation-contraction coupling, and L-type channels are predominant in cardiac myocytes. They regulate calcium influx, which is crucial for myocardial contraction. T-type channels, although less prevalent in hearts, contribute to pacemaker activity and may influence heart rhythm. Potassium channels, including voltage-gated and inward rectifier channels, are crucial for maintaining the resting membrane potential and regulating action potential duration. Dysfunction of potassium channels are associated with arrhythmias and cardiac pathologies like long QT syndrome. Additionally, the Na+-K+ pump maintains cellular ion gradients essential for various physiological processes. Understanding the structure and function of these ion channels provides insights into cardiac physiology and pathophysiology, guiding the development of targeted therapies for heart disorders.