📌 Professor’s Notes: Quick Revision
High-yield revision notes for rapid review before university examinations.
- Cardiac electrophysiology explains how electrical impulses are generated, conducted, and coordinated to produce effective cardiac contraction. The heart contains fast-response and slow-response action potentials, each adapted to a specific physiological function. Atrioventricular (AV) nodal delay ensures proper timing between atrial and ventricular contraction, allowing optimal ventricular filling.
- Cardiac electrical activity depends on the movement of sodium (Na⁺), calcium (Ca²⁺), potassium (K⁺), and pacemaker (If) currents.
- Na⁺ current (INa): Produces rapid depolarization (Phase 0) in atrial muscle, ventricular muscle, and Purkinje fibers.
- L-type Ca²⁺ current (ICaL): Produces the plateau phase in working myocardium and depolarization in nodal tissue.
- T-type Ca²⁺ current (ICaT): Contributes to pacemaker depolarization.
- K⁺ currents: Maintain resting membrane potential and produce repolarization.
- Pacemaker current (If): Generates spontaneous depolarization in pacemaker cells.
- Fast-response action potentials occur in atrial muscle, ventricular muscle, and Purkinje fibers and consist of five phases:
- Phase 0: Rapid depolarization due to Na⁺ influx.
- Phase 1: Initial repolarization due to transient K⁺ efflux.
- Phase 2: Plateau phase caused by balance between Ca²⁺ influx and K⁺ efflux.
- Phase 3: Final repolarization due to K⁺ efflux.
- Phase 4: Stable resting membrane potential maintained mainly by K⁺ conductance.
- Slow-response action potentials occur in the SA node and AV node.
- They contain three phases (0, 3, and 4); Phases 1 and 2 are absent.
- Phase 0: Ca²⁺ influx through L-type calcium channels.
- Phase 3: K⁺ efflux.
- Phase 4: Pacemaker potential (prepotential) produced by reduced K⁺ efflux, activation of If (funny current), and T-type Ca²⁺ influx. The slope of Phase 4 determines heart rate.
- Pacemaker potential is responsible for the automatic rhythm of the SA node. The If current, carried through hyperpolarization-activated cyclic nucleotide-gated (HCN) channels, initiates spontaneous depolarization. Sympathetic stimulation increases the slope of the pacemaker potential and increases heart rate, whereas parasympathetic (vagal) stimulation hyperpolarizes pacemaker cells, decreases the slope, and slows heart rate.
- Cardiac excitation normally begins in the SA node, spreads through the atria to the AV node, then passes through the His bundle, bundle branches, and Purkinje fibers to activate the ventricles. The atria and ventricles are electrically insulated by the fibrous cardiac skeleton, so impulses reach the ventricles only through the AV node.
- AV nodal delay (about 0.1 second) results from slow calcium-dependent conduction, small nodal cells, and fewer gap junctions. It allows complete atrial contraction before ventricular systole and protects the ventricles from excessively rapid atrial impulses, such as in atrial fibrillation. Purkinje fibers conduct impulses most rapidly (≈4 m/s), ensuring synchronous ventricular contraction.
📝 Practice MCQs
🎙️ Frequently Asked Viva Questions
High-yield viva questions with concise answers for rapid university examination preparation.
Q1. What are the two types of cardiac action potentials and where are they found?
Answer: Fast-response action potentials occur in atrial muscle, ventricular muscle, and Purkinje fibers. Slow-response action potentials occur in the SA and AV nodes.
Q2. Why is conduction slow in the AV node?
Answer: AV nodal cells are small, have few gap junctions, and depend mainly on slow L-type calcium channels instead of fast sodium channels.
Q3. What is the physiological importance of AV nodal delay?
Answer: It allows atrial contraction to finish before ventricular contraction, ensuring adequate ventricular filling and efficient cardiac output.
Q4. What is the ionic basis of Phase 0 of the ventricular action potential?
Answer: Rapid sodium influx through voltage-gated sodium channels produces the rapid depolarization (Phase 0).
Q5. What is the ionic basis of the plateau (Phase 2) of the ventricular action potential?
Answer: The plateau is produced mainly by calcium influx through L-type calcium channels, balanced by outward potassium movement.
Q6. What is the ionic basis of Phase 3 repolarization?
Answer: Closure of calcium channels and potassium efflux through delayed rectifier potassium channels restore the resting membrane potential.
Q7. Why do SA nodal cells have no true resting membrane potential?
Answer: SA nodal cells show spontaneous diastolic depolarization (pacemaker potential), so their membrane potential continuously drifts toward threshold.
Q8. What is the pacemaker potential?
Answer: The slow spontaneous depolarization during Phase 4 that brings SA nodal cells to threshold and initiates the next heartbeat.
Q9. What is the ionic basis of the pacemaker potential?
Answer: It results from reduced potassium efflux, activation of the funny (If) current, and calcium influx through T-type calcium channels.
Q10. What is the funny current (If)?
Answer: The If current is a slow inward sodium–potassium current through HCN channels that initiates spontaneous pacemaker depolarization.
Q11. How does sympathetic stimulation increase heart rate?
Answer: It steepens the slope of the pacemaker potential by increasing cAMP and calcium channel activity, allowing threshold to be reached sooner.
Q12. How does vagal stimulation decrease heart rate?
Answer: Acetylcholine hyperpolarizes SA nodal cells, increases potassium efflux, and decreases calcium entry, slowing pacemaker depolarization.
Q13. Why is conduction fastest in Purkinje fibers?
Answer: Purkinje fibers have a large diameter and rapid depolarization, giving them the highest conduction velocity (about 4 m/s).
Q14. Why is the plateau phase important in cardiac muscle?
Answer: It prolongs the action potential, allowing sustained contraction and preventing tetanic contraction of the heart.
Q15. How does electrical excitation normally spread through the heart?
Answer: SA node → atria → AV node → His bundle → bundle branches → Purkinje fibers → ventricular myocardium.
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