Lecture 7: Cardiac Muscle Tissue Flashcards
Describe the “First Half” of blood’s journey through the heart.
- Deoxygenated Blood enters the heart through the Superior Vena Cava (for head and upper extremities), or through the Inferior Vena Cava for lower extremities.
- The blood is funneled into the Right Atrium, and pushed through the Tricuspid Valve.
- After passing the tricuspid valve, the blood enters the Right Ventricle until it gets pushed up the Pulmonary Valve into the Pulmonary Artery
- The pulmonary artery carries the blood off into the lungs
Describe the “Second Half” of blood’s journey through the heart.
- Oxygenated blood reenters the heart through the Pulmonary Vein.
- The vein delivers the blood to the Left Atrium, where it is pushed through the Mitral Valve
- After passing through Mitral Valve, Blood sits in the Left Ventricle.
- From the Left Ventricle, the blood passes through Aortic Valve into the Aorta. From there, the Aorta delivers the oxygenated blood back into both the upper and lower extremities.
Describe the features and characteristics of Cardiac Muscle Tissue. (Be able to compare it against skeletal muscle tissue)
- Sarcomeric arrangement (therefore, striated)
- Mononucleated
- Central nuclei
- Syncytium
- Intercalated discs
- Cells may branch
How is the action potential different in cardiac muscle fiber?
- Averages about 105 mV, and can rise from about -85 to + 20 mV
- The potential stays fully depolarized for about 0.2 seconds. Unlike skeletal muscle tissue, which is much faster, this is a very long time span for a cell.
- The cardiac muscle cell undergoes sudden repolarization following the depolarization plateau.
How do skeletal muscle fibers compare to cardiac muscle fiber with regard to the T-Tubules and sarcoplasmic reticulum?
- In cardiac muscle, T-tubules are found along the z-line rather than at the ends of the thick filaments.
- There is only one cisterna per T-tubule instead of two
- T-tubules form Diads with the sarcoplasmic reticulum instead of triads
- The sarcoplasmic reticulum isn’t as extensive or prominent in cardiac muscle
- Cardiac muscle cells form a synctium
There are two types of cardiac action potentials: Fast and Slow.
Describe the Fast one.
- Found in atria, ventricles and conduction system
- Very rapidly conducting but non-contractile in Purkinje fibers
- Rapidly conducting and contractile in atrial and ventricular fibers
- High amplitude (100 mV)
- These conduct well, but don’t contract well.
- Fast action potentials are due to changes in conductance of potassium, sodium, and calcium ions.
- Conductance pattern is mostly due to voltage dependent gates.
Things that result in a faster conduction velocity:
Greater AP amplitude, More rapid rate of rise of phase 0, and Larger cell diameter
There are two types of cardiac action potentials: Fast and Slow.
Describe the Slow one.
- Found in SA and AV nodal tissues
- Conducts slowly
- Automatically depolarizes during resting phase, and more rapidly in the SA node than in the AV node
- Low amplitude (60 mV)
- These conduct slowly but rapidly contract
- No fast sodium ion gates
- Upstroke (negative to positive) of action potential is due to calcium (therefore it proceeds slowly).
- Resting phase potential 4 is close to -60 mV rather than -90 mV characteristic of fast action potentials.
- Change in potential (amplitude) is less than that for fast action potentials.
- SA and AV nodal tissue will spontaneously depolarize slowly to reach threshold during phase 4 (resting phase).
Describe each of the phases of a cardiac muscle action potential (See Lecture 7 - Slide 21 for further diagram)
-Phase 4: Resting potential
-Phase 0: Rapid depolarization
-Phase 1: Initial, incomplete repolarization
-Phase 2: Plateau or slow decline of membrane potential
-Phase 3: Repolarization
Why it’s out of order, I have no idea.
So it should go from 4 to 0 to 1 to 2 to 3 back to 4.
Compare the characteristics between:
- Fast-type contractile myocytes
- Fast-type non-contractile myocytes
- Slow-type non-contractile myocytes
- Large diameter, High amplitude, Rapid onset of action potential
- Very large diameter, Very rapid upstroke
- Small diameter, Low amplitude, Slow rate of depolarization
Explain the role of calcium, sodium, and potassium ions in the creation of the cardiac muscle action potential plateau (26)
In skeletal muscle, the sodium channels close rapidly.
- In cardiac muscle the sodium channels also close rapidly, but the calcium channels open slowly and stay open for a longer period of time.
- In cardiac muscle there is also a delay in the opening of the potassium channels.
- The large concentration of both calcium ions and potassium ions is responsible for the plateau.
Describe the automaticity of the heart (29)
Some cardiac tissues will gradually depolarize during phase 4, eventually reaching threshold.
- These tissues include the SA and AV nodes and the Purkinje fibers.
- The SA node usually depolarizes more rapidly than the others and reaches threshold first and, by default, becomes the normal “pacemaker” of the heart’s rhythmicity.
- Rate of depolarization determines the rhythmicity of the cell.
- Gradual depolarization during phase 4 is due to:
- Special sodium channels which open following phase 3
- SA = Sinoatrial; SA node has the fastest intrinsic pulsation rate.
Describe the resting membrane potential of a resting node fiber
- 55 to -60 mV (Threshold ≈ -40 mv) (That’s a postive 55)
- Fast sodium channels are already inactivated (blocked).
- Inactivation gates close when membrane potential is less negative than -55 mV.
- Therefore, only slow sodium-calcium channels can open.
- Therefore, atrial nodal action potential is slower to develop.
- Therefore, repolarization is also slower.
- There is a slow leak of sodium ions back into the cells.
- Membrane potential becomes more positive.
- At -40 mV, sodium-calcium channels become activated.
- Sodium-calcium channels are inactivated within 100-150 msec after opening.
- Large numbers of potassium channels open at the time the sodium calcium channels become inactivated.
- Nodal cells become repolarized.
- Potassium channels remain open for a few tenths of a second.
What’s the resting potential of a ventricular fiber?
-85 to -90 mV
What are the exchanging roles and relationships between Ca, K, and Na? (See slide 34 and memorize the fuck out of it)
In a sinus nodal fiber:
- Sodium influx at phase 4
- Calcium influx at phase 0
- Potassium Efflux at phase 3.
In a Ventricular Muscle Fiber:
This doesn’t have as obvious of phases, so this’ll be harder…but:
- Sodium Influx when it shoots up
- Fast Potassium efflux at the peak
- Calcium influx for the first phase of repolarization (at this point potassium is at equilibrium in and out.
- Delayed Potassium efflux during the downward peak.
Christ i suck at this.
Describe the SA node’s role as a pacemaker
- Action potentials originating in the SA node generate a “sinus” rhythm.
- Action potentials that originate anywhere else are said to be from an ectopic focus or pacemaker