Physiology · MU Sofia

23. Excitation-Contraction Coupling in the Working Myocardium.Mechanics of cardiac contraction.

Explains excitation-contraction coupling in working cardiac muscle, starting with calcium-induced calcium release from the sarcoplasmic reticulum. It then walks through the cardiac action potential phases, linking the plateau to calcium influx and troponin-driven contraction. The note closes with the length-tension relationship, the force-velocity relation under afterload, and the Frank-Starling law, followed by recap questions on relaxation and heart failure.

Inside: 1 section · 3 labelled pictures · 11 flashcards · 4 min

Topic 23 of 104 in the MU Sofia syllabus for Physiology (Dental Medicine, Year 2). The free AceMed note covers it in 1 section, about 521 words (4 min of reading), with 11 flashcards.

In this note

  1. Introduction

Introduction

23. Excitation-Contraction Coupling in the Working Myocardium.Mechanics of cardiac contraction.

1. Overview of Excitation-Contraction (E-C) Coupling in Cardiac Muscle

Excitation-contraction (E-C) coupling in cardiac muscle is the process that links an action potential (electrical excitation) to muscle contraction.

Calcium-Induced Calcium Release (CICR): In cardiac muscle, small amounts of Ca²⁺ enter the cell during an action potential, triggering a larger release of Ca²⁺ from internal stores (sarcoplasmic reticulum, SR). This amplification is unique to cardiac muscle and essential for strong contraction.

2. Phases of the Cardiac Action Potential

Phase 0 (Depolarization):

The action potential begins with a rapid influx of Na⁺ through voltage-gated Na⁺ channels, causing cell depolarization. The action potential peaks at +30mV then Na+ gates close.

Phase 1 (Initial Repolarization):

Brief outward flow of K⁺ ions causes slight repolarization, setting the stage for Ca²⁺ influx.

Phase 2 (Plateau Phase):

L-type Ca²⁺ Channels Open: Ca²⁺ enters the cell, balancing K⁺ efflux. This plateau prolongs the action potential.

Significance: The plateau phase allows sustained Ca²⁺ influx, critical for prolonged contraction and effective pumping.

Ca2+ binds to troponin which moves the tropomyosin so that the binding site is exposed to myosin heads.

The myosin heads then perform the power-stroke and pulls the actin towards the center of the sarcomere. This is the contraction of the muscle

Phase 3 (Repolarization):

Ca²⁺ channels close, while K⁺ channels stay open, causing repolarization and returning the cell to resting potential.

Phase 4 (Resting Potential):

The Na⁺/K⁺ ATPase pump restores ion balance, expelling Na⁺ and bringing K⁺ back into the cell.

3. Calcium-Induced Calcium Release (CICR)

Ca²⁺ Entry via L-type Channels: Ca²⁺ enters through L-type Ca²⁺ channels in response to the action potential during the plateau phase.

Ryanodine Receptors (RyR2) on the SR: The incoming Ca²⁺ activates RyR2 on the SR, triggering the release of a larger quantity of Ca²⁺ into the cytoplasm.

Amplification of Signal: This release of Ca²⁺ from the SR amplifies the initial Ca²⁺ signal, providing enough Ca²⁺ for full contraction.

Termination: CICR stops when SR Ca²⁺ levels are depleted or L-type channels close, halting Ca²⁺ entry.

Mechanics of Cardiac Contraction

1. Length-Tension Relationship

Optimal Length: The heart muscle generates maximum force when fibers are stretched to an ideal length (length-tension relationship).

Physiological Relevance: This relationship ensures efficient pumping by optimizing cross-bridge overlap between actin and myosin.

2. Force-Velocity Relationship.

Effect of Afterload: As afterload (arterial resistance) increases, contraction velocity decreases.

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