CV 3

Objectives

  • Understand the ionic basis of action potentials in contractile cardiac myocytes.
  • Comprehend how the Electrocardiogram (ECG) is generated and interpret its components.

Ionic Basis of an Action Potential for Contractile Cardiac Myocytes

  • Characterized by 5 phases of depolarization and repolarization:
    1. Phase 0: Rapid Depolarization
    • Triggered by Na+ influx through fast voltage-gated Na+ channels.
    • Occurs following the pacemaker potential reaching the threshold of approximately -65 mV.
    1. Phase 1: Early Repolarization
    • Known for rapid inactivation of fast Na+ channels.
    • Involves activation of transient outward K+ current resulting in a brief efflux of K+.
    1. Phase 2: Plateau Phase
    • Characterized by a balance between K+ efflux and Ca2+ influx through the L-type Ca2+ channels.
    • K+ efflux occurs through delayed rectifier K+ channels.
    • Duration of this phase is approximately 175 ms.
    1. Phase 3: Repolarization
    • Continuation of K+ efflux leads to a progressively negative inside of the cell.
    • Duration is about 75 ms, and the cell is refractory during phases 0, 1, 2, and part of 3 due to inactivation of L-type Ca2+ channels.
    1. Phase 4: Restoration of Ionic Concentrations
    • Returns Na+ and K+ to resting concentrations via Na+-K+ pumps (Na+-K+ ATPase).
    • Ca2+ restoration through Na+-Ca2+ exchangers and ATP-driven Ca2+ pumps, with a net movement of 2 K+ entering and 3 Na+ leaving the cell.

Heart Structure and Details

  • Catecholamines play a significant role in cardiac contraction.
  • Calcium (Ca2+) interactions are crucial in muscle contraction, via binding to troponin I, influencing muscle fibers.
  • Cardiac glycosides inhibit the Na+-K+ pump, affecting intracellular Na+ levels.

Electrocardiogram (ECG/EKG)

  • Definition: A graphical representation of biopotentials generated during the cardiac cycle, reflecting electrical events of depolarization and repolarization, subsequently triggering mechanical contraction and relaxation.
  • Key Components:
    • P Wave: Atrial depolarization.
    • QRS Complex: Ventricular depolarization.
    • T Wave: Ventricular repolarization.
    • U Wave: Unknown, possibly related to repolarization of papillary muscles or Purkinje fibers.
  • Lead Connections:
    • Bipolar Leads: Leads I, II, III (constructed through references of right arm to left arm leg connections).
    • Unipolar Leads: aVR, aVL, aVF, and leads V1-V6.

ECG Placement of Electrodes

  • Limb Leads:
    • Lead I: RA (-) to LA (+)
    • Lead II: RA (-) to LL (+)
    • Lead III: LA (-) to LL (+)
  • Chest Leads: V1 to V6 positioned across the chest to capture electrical activity from the heart's surface.

ECG Intervals or Segments

  • PR Interval: Time taken for impulse from SA node to start of ventricular depolarization (normal 0.12 to 0.20 seconds).
  • QRS Duration: Reflects the time required for ventricular depolarization (should be < 0.12 seconds).
  • QT Interval: Duration from ventricular depolarization to repolarization; can be corrected for heart rate as QTc. Normal range is 0.3 - 0.44 seconds.
  • ST Segment: Indicates the period between ventricular depolarization and repolarization (isoelectric line). Deviations can indicate ischemia.
  • T Wave: Normally upright; an inverted T wave may signal ischemia or conduction issues.

Sample Questions

  1. What is the cause of the plateau phase observed in the myocardial action potential?
    • Answer: c) Eflux of K+ and influx of Ca++.
  2. What does the QRS complex represent in the ECG?
    • Answer: a) Ventricular depolarization.
  3. Duration of the QT interval can indicate what relative to heart rate?
    • QTc = QT/extsqrt(RR)QT / ext{sqrt} (RR) and is affected by HR.
  4. PR segment status can suggest conduction delay if prolonged, indicating possible arrhythmias.

Normal ECG Values

  • P wave: Amplitude < 2.5 mm, width < 0.11 s.
  • Short PR interval may indicate pre-excitation syndrome.
  • Long PR interval might suggest heart block.
  • Ensure adequate monitoring of QT interval especially in drug administration settings to avoid long QT syndrome.