Cardiac muscle is essential for the functioning of the heart.
Silverthorn 8e – Chapter 12 (Cardiac Muscle) Section 12.4.
Chapter 14 – Section 4.3 "Cardiac Muscle and the Heart", Pages 408-409.
Beginning at subsection "Cardiac Muscles Contract Without Innervation" on page 446.
Roles of three types of cardiac muscle cells in generating electrical activity.
Similarities and differences between cardiac action potentials and neuronal action potentials; implications on tetanus.
Explanation of Excitation-Contraction Coupling in cardiac contractile cells.
Types of cardiac muscle cells
Electrical conduction in the heart
Action potentials in pacemaker cells vs. contractile cells
Prolonged action potentials in contractile cells
Mechanism of Excitation-Contraction Coupling.
Cardiac muscle cells (myocytes) are approximately 0.1 mm in diameter.
Contains a nucleus and intercalated discs that link the cells.
Interconnected Structure:
They form functional syncytia, allowing for synchronized contractions.
Types of Membrane Junctions in Intercalated Discs:
Desmosomes: Provide structural support during contractions.
Gap Junctions: Allow electrical signals to pass quickly between cells.
Myocardial Autorhythmic Cells
Initiate and maintain electrical activity.
Do not contract.
Conducting Cells
Conduct electrical signals throughout the heart.
Also do not contract.
Myocardial Contractile Cells
Comprise 99% of cardiac muscle cells.
Responsible for contractions and the mechanical pumping of the heart.
Electrically joined by gap junctions.
Origin of Cardiac Impulse: Begins at the SA node.
Action Potential Spread:
Spreads through left and right atria.
Passes from atria to ventricles via the AV node (only electrical contact point).
Delays briefly at AV node for complete ventricular filling.
Impulse Pathway:
Travels rapidly down the interventricular septum (bundle of His).
Disperses throughout myocardium via Purkinje fibers.
Activated via cell-to-cell spread through gap junctions.
Intrinsic Conduction System:
Autorhythmic cells initiate action potentials.
No stable resting membrane potential; rather, a pacemaker potential that drift towards threshold.
Membrane repolarizes to -60 mV.
Ion Currents in Pacemakers:
IF: Sodium (Na+) current.
ICaT: Fast calcium (Ca2+) current.
ICaL: Slow Ca2+ current.
Rising phase due to calcium influx through L-type Ca2+ channels.
Characterized by:
Rapid depolarization.
Rapid partial early repolarization.
Prolonged slow repolarization (plateau phase).
Rapid final repolarization.
Important for maintaining contraction duration.
Prolonged Action Potential:
Caused primarily by slow calcium channel activation (L-type).
Ensures adequate blood ejection and prevents tetanus.
Skeletal Muscle:
Short refractory period; allows summation and tetanus.
Cardiac Muscle:
Long refractory period close to entire muscle twitch duration; prevents tetanus.
Long action potentials lead to an extended refractory period, preventing tetanus and ensuring rhythmic heartbeats.
Mechanism Explained:
Ca2+ entry through T tubules triggers massive Ca2+ release from the sarcoplasmic reticulum (SR).
This leads to cross-bridge cycling and muscle contraction.