Section 3 Flashcards

1
Q

What is unique about the heart as an organ?

A

The heart is an electro-mechanical organ, possessing both electrical activity, similar to nerves, and the ability to contract as a large muscle.

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2
Q

How many types of cardiac muscle cells exist, and what are their primary functions?

A

There are two types of cardiac muscle cells: primarily contractile cells responsible for mechanical work, and electrical cells responsible for generating and propagating action potentials.

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3
Q

What is the primary function of primarily contractile cells in the heart?

A

Primarily contractile cells perform the mechanical work of the heart.

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4
Q

What are some situations where the SNS or PNS could affect heart rate?

A

Physical and emotional stress can cause changes in heart rate. This stress can be due to exercise, fear,
injury, and even illness.

  • Exercise increases heart rate to bring additional blood, and therefore oxygen, to working muscles and to rid them of CO2 and other waste.
  • Fear increases heart rate due to the “fight or flight” response which releases epinephrine from the adrenal glands. Epinephrine stimulates the SNS and raises the heart rate.
  • Illness and injury cause an increase in blood flow to peripheral tissues, which increases heart rate via the SNS.
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5
Q

Does the heart require the CNS or PNS to generate or propagate electrical signals?

A

No

What makes the heart interesting in terms of electrical activity is that it generates and propagates electrical signals independently. That is, the heart is not dependent upon either the CNS or PNS for its function.

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6
Q

What are specialized cardiac muscle cells capable of generating action potentials known as?

A

Autorhythmic cells.

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7
Q

How do autorhythmic cells differ from other cells in terms of resting membrane potential?

A

Autorhythmic cells have a slowly depolarizing resting membrane potential until the threshold is reached and an action potential is fired.

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8
Q

What is the suggested mechanism for depolarization in autorhythmic cells, and what channels are thought to be involved?

A

Autorhythmic cells may contain If channels, possibly activated by the hyperpolarization-activated cyclic nucleotide-gated channel (HCN) family or the T-type Ca2+ channel.

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9
Q

What is unique about the upstroke of the action potential in autorhythmic cells compared to neurons and cardiac contractile cells?

A

The upstroke of the action potential in autorhythmic cells is due to the L-type Ca2+ channel, unlike neurons and cardiac contractile cells where it is typically due to Na+ channels.

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10
Q

Where are autorhythmic cells localized in the heart?

A

Autorhythmic cells are localized in specific regions of the heart, including the sinoatrial (SA) node.

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11
Q

Where is the sinoatrial (SA) node located?

A

The sinoatrial (SA) node is a very small area located in the right atrial wall near the opening of the superior venae cavae.

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12
Q

What is the If channel?

A

A channel with unusual properties that allow current (I) to flow

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13
Q

Where are sinoatrial (SA) nodes located?

A

Sinoatrial (SA) nodes are located in a very small area in the right atrial wall near the opening of the superior venae cavae.

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14
Q

Where is the atrioventricular (AV) node located, and how is it often described?

A

The atrioventricular (AV) node is a small area located in the right atrium, where the right atria and right ventricle come together. It is often described as being located in the interatrial septum due to its central position in the heart.

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15
Q

What does the bundle of His consist of, and where does it arise from?

A

The bundle of His consists of specialized cells that arise from the AV node.

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16
Q

Where do the bundle branches of the bundle of His travel, and what is their path in the heart?

A

They travel down each side of the septum to the bottom of the heart, where they curve around and travel back towards the atria.

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17
Q

What is the path and location of the Purkinje fibers?

A

Purkinje fibers are small fibers that branch off the bundle of His and spread along the inner (endocardial) surface of the ventricles.

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18
Q

What is the role of autorhythmic cells in the SA node?

A

pacemaker cells of the heart, as they have the fastest rate of depolarization, controlling heart rate at around 70-80 beats/minute for the average person.

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19
Q

Why are SA node cells considered pacemaker cells?

A

because they control heart rate and have the fastest rate of depolarization, reaching threshold the fastest.

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20
Q

What happens once an action potential is generated in SA node cells?

A

it conducts through the rest of the cardiac conduction system, overriding the pacemaker activity of other autorhythmic cells.

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21
Q

What is the significance of the pacemaker activity of the SA node?

A

As long as the SA node is functioning fine, it controls the rate at which the heart beats. Without pacemaker activity, the heart would not beat at all

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22
Q

Why should atrial excitation and contraction be complete before the onset of ventricular contractions?

A

Atrial excitation and contraction should be complete before the onset of ventricular contractions to allow the ventricles to fill with blood completely. If ventricular contraction occurred simultaneously with atrial contraction, incomplete ventricular filling would occur.

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23
Q

What percentage of total ventricular filling is accounted for by passive blood flow, and when does it occur?

A

Passive blood flow accounts for around 80% of total ventricular filling, occurring during the relaxation of the heart when the AV valves are open.

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24
Q

Why is it crucial for excitation of cardiac muscle fibers to be coordinated?

A

Coordination of excitation is crucial for efficient pumping, as uncoordinated depolarization (ventricular fibrillation) can hinder the heart’s ability to eject blood.

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25
Q

What is ventricular fibrillation, and why is it problematic?

A

Ventricular fibrillation is uncoordinated depolarization of different regions of a ventricular wall, hindering the heart’s ability to eject blood.

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26
Q

Why must the pair of atria and the pair of ventricles be functionally coordinated?

A

The pair of atria and the pair of ventricles must be functionally coordinated to ensure both pumps work together, moving the same amount of blood at the same time for efficient blood circulation.

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27
Q

What do you think would happen if the ventricles contracted out of sync?

A

If the right and left ventricles contract at different times, such as is the case with a bundle branch block (a block in one of the branches of the bundle of His), the blood pumping to the lungs to be oxygenated,and the blood pumping through the aorta would occur at different times.

These blocks can cause unnecessary stress on the ventricular walls and may require a pacemaker to re-coordinate the
contraction of the ventricles.

Alone, these blocks are generally not dangerous, however they can be a symptom of a much larger
problem such as a heart failure, a valve problem, lung disease, or other cardiac conditions.

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28
Q

What are the two main mechanisms by which the wave of excitation travels throughout the atria?

A

The wave of excitation travels throughout the atria by gap junctions and pathways (interatrial and internodal pathways).

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29
Q

What are gap junctions, and how do they contribute to atrial excitation?

A

Gap junctions are connections between atrial cells that allow the wave of excitation to spread through the atria.

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30
Q

What is the function of the interatrial pathway in atrial excitation?

A

The interatrial pathway extends from the right atrium to the left atrium, ensuring that the wave of excitation spreads across both atria at the same time, allowing them to contract simultaneously.

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31
Q

What is the role of the internodal pathway in atrial excitation?

A

The internodal pathway connects the SA node to the AV node, facilitating the transmission of the excitation wave between these two nodes.

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32
Q

What separates the muscle cells of the atria from the muscle cells of the ventricles, and what is its significance?

A

The muscle cells of the atria are separated from the muscle cells of the ventricles by a dense region of connective tissue. This separation limits the means by which an electrical signal can move from the atria to the ventricles, allowing only the AV node and the bundle of His to transmit the signal.

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33
Q

Why does the rate of conduction slow down through the AV node, and what is this delay called?

A

The rate of conduction slows down through the AV node, and this delay is called the AV nodal delay. The purpose of this delay is to ensure that the atria have had a chance to contract prior to the ventricles, maximizing the atrial emptying of blood into the ventricles.

34
Q

Why can’t the ventricles rely on gap junctions alone to spread the wave of excitation?

A

The ventricles, being a substantially larger mass of muscle than the atria and having a different shape, would result in the top part of the heart contracting before the wave of excitation reached the bottom if they relied on gap junctions alone

35
Q

What solves the problem of coordinating the contraction of the ventricles (which can’t only be done with gap junctions), and how?

A

The bundle of His and the purkinje fibers solve the problem of coordinating ventricular contraction. They allow the wave of excitation to spread uniformly through the ventricles.

36
Q

What happens after the AV nodal delay in ventricular excitation?

A

After the AV nodal delay, the wave of excitation spreads down both the right and left bundles of His and the purkinje fibers.

37
Q

Why is gap junction communication required in ventricular excitation, especially with purkinje fibers?

A

Purkinje fibers do not terminate on all ventricular muscle cells, so gap junction communication is required to spread the wave of excitation to the rest of the cells not innervated by purkinje fibers.

38
Q

What does the ventricular conduction system ensure in terms of ventricular contraction?

A

The ventricular conduction system ensures that both ventricles contract at the same time.

39
Q

How is the cardiac action potential different in shape compared to nerve cells and pacemaker cells of the SA node?

A

The cardiac action potential is substantially different in shape due to the different kinds of voltage-gated ion channels found in ventricular muscle cells compared to nerve cells and pacemaker cells of the SA node.

40
Q

What is the resting membrane potential for a cardiac myocyte, and why does it remain steady until the cell is excited?

A

The resting membrane potential for a cardiac myocyte is around -80 mV. It remains steady until the cell is excited because these cells have no pacemaker currents.

41
Q

What are the three stages of the cardiac action potential?

A
  1. When a cardiac myocyte is excited and reaches threshold, voltage-gated Na+ channels open, and the membrane potential rapidly depolarizes towards +50 mV.
  2. This rapid depolarization activates other ion channels, creating a balance of the membrane potential known as the plateau potential.
  3. Eventually, the transient outward K+ and L-type Ca2+ currents inactivate, allowing the cell to hyperpolarize and reach its resting membrane potential again.
42
Q

What creates the balance of the membrane potential during the plateau phase of the cardiac action potential?

A

The balance of the membrane potential during the plateau phase is created by the activation of transient outward K+, L-type Ca2+, and delayed rectifying K+ channels.

43
Q

What is excitation-contraction (EC) coupling, and what is its role in cardiac myocytes?

A

Excitation-contraction (EC) coupling is the process by which an action potential triggers a cardiac myocyte to contract. It plays a crucial role in initiating muscle contraction.

44
Q

How is the T-tubule system involved in cardiac EC coupling, and what is its role in skeletal muscle cells?

A

Like skeletal muscle cells, cardiac myocytes have a well-defined T-tubule system. In skeletal muscle cells, T-tubules allow the spread of excitation and an increase in intracellular Ca2+ necessary for contraction.

45
Q

What happens during the plateau phase of the action potential in cardiac contractile cells, and where are the L-type Ca2+ channels located?

A

During the plateau phase, L-type Ca2+ channels located within the T-tubules open, allowing Ca2+ to enter the cell.

46
Q

How is Ca2+ released within the cell during cardiac EC coupling, and what is the process called?

A

The opening of L-type Ca2+ channels allows Ca2+ to enter the cell. This Ca2+ can directly interact with the contractile apparatus. Additionally, Ca2+-induced Ca2+-release (CICR) occurs when released Ca2+ interacts with ryanodine receptors on the sarcoplasmic reticulum (SR), triggering an additional large release of Ca2+ from internal stores.

47
Q

What initiates cardiac muscle contraction during EC coupling, and how does contraction end?

A

The influx of Ca2+ initiates cardiac muscle contraction. Contraction ends when Ca2+ is removed from the cytosol, either by moving it across the plasma membrane or pumping it back into the SR.

48
Q

Why can’t cardiac muscle undergo summation and tetanus like skeletal muscle fibers?

A

Cardiac muscle cannot undergo summation and tetanus because it would lead to inefficient and life-threatening contractile patterns in the heart.

49
Q

What prevents twitch summation in cardiac muscle, and why does this occur?

A

The length of the cardiac action potential, particularly the prominent plateau phase, prevents twitch summation. During the plateau phase, the depolarized membrane potential keeps the voltage-gated Na+ channels in an inactivated state, preventing re-stimulation even if another wave of excitation occurs.

50
Q

What is the refractory period, and why is it significant in cardiac muscle contraction?

A

The refractory period is the period during which a cardiac myocyte cannot be re-stimulated. It is significant in cardiac muscle contraction because it prevents additional waves of excitation during the plateau phase, ensuring that most of the muscle contraction is completed before re-stimulation can occur.

51
Q

Why is it more sensible to study the electrical and mechanical properties of the heart as a whole rather than at the single myocyte level?

A

Studying the heart as a whole is more sensible because the heart is highly coordinated, serving the single function of contracting to circulate blood. Examining the organ’s electrical and mechanical properties at this level provides a more comprehensive understanding.

52
Q

What generates the electrical field in the heart, and how is it transmitted throughout the body?

A

The distinctive pattern of electrical activity in the heart generates an electrical field. This field is transmitted throughout the body fluids and can be “sensed” at the surface of the skin.

53
Q

What is the abbreviation for the technique used to study the electrical activity of the heart, and what does it stand for?

A

The technique used to study the electrical activity of the heart is abbreviated as ECG, which stands for Electrocardiogram.

54
Q

How did Willem Einthoven construct the first ECG device, and what was its key feature?

A

Einthoven constructed a device using three electrical leads placed on the right arm, left arm, and left leg, with a ground electrode on the right leg. This arrangement formed the Einthoven Triangle for lead location and serves as the basis for the limb leads of the modern ECG.

55
Q

How does the modern ECG differ from the original three leads developed by Einthoven?

A

The modern ECG consists of a 12 lead ECG, expanding beyond the original three limb leads. It incorporates three limb leads (I-III) and six leads on the chest around the heart. The additional three leads are mathematically derived from leads I, II, and III.

56
Q

What is the purpose of the 12 lead ECG, and how many physical leads does it use?

A

The 12 lead ECG is a powerful diagnostic tool that measures the electrical activity of the heart. Despite its name, it arises from only 9 physical leads. Three leads are limb leads (I-III), and the remaining six are positioned on the chest around the heart.

57
Q

How does an ECG measure the electrical activity of the heart, and what does it allow us to observe?

A

An ECG measures changes in electrical potentials that originate in the heart and are transmitted through the body to the surface, where they are measured. It allows the observation of the summation of all electrical activity at any given time, enabling the identification of cardiac abnormalities.

58
Q

What is the nomenclature used for different parts or deflections of an ECG recording, and what is the reference line for ECG tracings?

A

The nomenclature for ECG deflections was introduced by Einthoven. ECG tracings revolve around the isoelectric, or 0 voltage line.

59
Q

What does an upward (positive) deflection generally indicate in an ECG tracing, and what does a downward (negative) deflection indicate?

A

Generally, depolarization is observed as upward (positive) deflections, while repolarizations are observed as downward (negative) deflections.

60
Q

What does the P wave in an ECG tracing represent, and what initiates it?

A

The P wave represents the depolarization of the atria. It is initiated by the firing of the SA node, although the SA node’s electrical activity is too small to be detected at the body’s surface.

61
Q

What does the QRS complex in an ECG tracing represent, and what electrical event corresponds to it?

A

The QRS complex represents the depolarization of the ventricles. It corresponds to the wave of excitation traveling down the bundle of His and Purkinje fibers.

62
Q

What does the T wave in an ECG tracing represent, and what electrical event corresponds to it?

A

The T wave represents the repolarization of the ventricles.

63
Q

What do different segments of an ECG recording indicate?

A

Various segments of an ECG recording represent different phases of the cardiac cycle. For example, the P-R segment indicates the AV node delay, the S-T segment indicates the time during which ventricles are contracting and emptying, and the T-P interval indicates the time during which ventricles are relaxing and filling.

64
Q

T wave:
__________________

A

Ventricular repolarization

65
Q

P wave:
__________________

A

Atrial depolarization

66
Q

TP Interval:
__________________

A

Time during which ventricles are relaxing and filling

67
Q

ST segments:
__________________

A

Time during which ventricles are contracting and emptying

68
Q

ST segments:
__________________

A

Time during which ventricles are contracting and emptying

69
Q

QRS complex:
__________________

A

Ventricular depolarization (atria repolarizing simultaneously)

70
Q

PR Segment:
__________________

A

AV nodal delay

71
Q

QT interval:
__________________

A

Electrical depolarization and repolarization of the ventricles

72
Q

What is cardiac output?

A

The volume of blood that is pumped by each ventricle over a minute of time

73
Q

What is tachycardia, and what heart rate is considered tachycardic in adults?

A

Tachycardia is a heart rate that exceeds the normal resting heart rate. In adults, this is a heart rate exceeding 100 bpm.

74
Q

How can tachycardia affect cardiac output, and how is it classified based on the QRS complex in an ECG?

A

Tachycardia can decrease cardiac output due to reduced ventricular filling. It is classified into either wide or narrow based on the QRS complex in an ECG.

75
Q

What is extrasystole, and what initiates the heartbeat in this condition?

A

Extrasystole is an event where a heartbeat is initiated by the Purkinje fibers rather than the SA node.

76
Q

How does extrasystole affect ventricular contraction, and is it normally a threat to healthy individuals?

A

In extrasystole, the ventricles contract before the atria, leading to suboptimal filling, reducing cardiac output. It is not normally a threat to healthy individuals.

77
Q

What is ventricular fibrillation (V-fib), and what are the consequences of this condition?

A

Ventricular fibrillation occurs when the heart is quivering rather than pumping due to abnormal electrical activity in the ventricles. It can result in cardiac arrest with loss of consciousness and no pulse.

78
Q

How is ventricular fibrillation classified on an ECG, and what does the ECG show in this irregularity?

A

V-fib is classified by an irregular, unformed QRS complex without clear P waves on an ECG.

79
Q

What is a complete heart block, and what happens to the impulse generated at the SA node in this condition?

A

A complete heart block, or third degree AV block, is a condition where the impulse generated at the SA node does not travel to the ventricles. The pacemaker cells in the AV node independently activate the ventricles.

80
Q

How does a complete heart block appear on an ECG, and what are the consequences for patients with this condition?

A

On an ECG, a complete heart block shows a P wave with regular intervals, but the QRS complex does not always follow a P wave. Patients with complete heart block often experience abnormally low heart rates and blood pressure.

81
Q
A