Electrical properties of the heart Flashcards

1
Q

The potassium hypothesis

A
  • The membrane is more permeable to potassium ions than anything else and these can diffuse down a concentration gradient, carrying positive charge with them.
  • As they move, the incident chamber becomes increasingly positive related to the other chamber (as other negative ions cannot move due to the barrier being impermeable to them).
  • The electrical gradient then directly opposes the concentration gradient and eventually you get a point when the electrical gradient = the concentration gradient and equilibrium is achieved
  • Here K+ ions randomly move back and forth
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2
Q

What does the RMP depend on and how can the resting membrane potential be predicted?

A

The membrane potential depend on the flow of K+ out of cells.
Using the Nernst equation

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3
Q

What happens if the membrane is only permeable to K+?

A

If the membrane is only permeable to K+ then then potential across it will equal the K+ equilibrium potential.
The value for this is -80mV very close to actual RMP

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4
Q

What will cause the membrane’s potential to change?

A

The membrane’s potential will change depending on the relative permeability of the membrane to different ions

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5
Q

What happens if the membrane is only permeable to Na+?

A

When the membrane is only permeable to Na then the membrane potential is equal to the Na equilibrium potential.

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6
Q

What is a better equation to predict membrane potential over Nernst equation?

A

The membrane potential is better describe by the Goldman Hodgkin Katz equation which takes into account relative permeabilities of ions

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7
Q

What is the duration of a cardiac action potential and why?

A
  • Cardiac action potentials last between 200 and 400ms (long)
  • The duration of the AP controls the duration of contraction of the heart
  • > long, slow contraction is required to produce an effective pump
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8
Q

At rest what is membrane potential mainly determined by and why?

A
  • At rest, membrane potential determined by K+
  • Large membrane permeability to K+ stabilises membrane potential reducing risk to arrhythmias by requiring a large stimulus to excite the cells
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9
Q

Cardiac action potential sequence

A
  1. AP causes large change in PNa causing rapid upstroke
  2. Large [Na+] Intracellular inactivates Na channels and thus reduces PNa quickly and this causes a brief increase in PK which gives the characteristic notch on the graph as K leaves the cell. Na channels enter absolute refractory period.
  3. Large [Na+] intracellular also increases PCa early in plateau via LTCC. Influx provides trigger for Ca2+ release from intracellular stores for contraction.
  4. The Ca2+ intracellular increase combined with the K+ efflux maintains the plateau of the graph.
  5. Plateau ends when PCa decreases and a slow and small increase in PK occurs.
  6. Repolarisation occurs due to inactivation of LTCC and opening of another subtype of K+ channels.
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10
Q

What is absolute, relative refractory period?

A

Absolute - time during which no action potential can be initiated

Relative- period after ARP when and AP can be initiated but it must be larger than normal

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11
Q

What causes refractory periods?

A

Sodium channel inactivation which reactivate at repolarisation

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12
Q

What do long ARPs and RRPs prevent?

A

tetany

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13
Q

What is full recovery time?

A

The time at which a normal AP can be elicited with a normal AP.

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14
Q

Skeletal muscle vs cardiac muscle re stimulation and tetanising

A

In skeletal muscle repolarisation occurs quickly so restimulation and summation is possible

In cardiac muscle you cannot re excite the muscle until contraction is well underway to prevent tetanising the cardiac muscle

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15
Q

What are the phases of the AP?

A
phase 4- resting membrane potential
phase 0- upstroke
phase 1- early repolarisation
phase 2 -plateau
phase 3 - repolarisation
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16
Q

What are the intrinsic properties of the heart?

A
  • The heart has its own independent electrical impulse generation and propagation system.
  • The nature of the heart means even if disconnected with it’s supplying nerves; it can still beat.
  • The internal electrical activity is modulated by sympathetic and parasympathetic nerves.
17
Q

What happens during phase 1?

A

Inactivation of sodium channels (no further depolarisation) and the transient outward potassium current starting.

18
Q

What happens during phase 2?

A
  • Large intracellular sodium causes calcium influx which triggers CICR from intracellular stores.
  • Potassium efflux and calcium influx stabilise the membrane potential around 0mV.
  • Calcium influx can be blocked by dihydropyridine calcium channel antagonists (bind to LTCC, blocking the channel) such as Nifedipine, Nitrendipine and Nisoldipine.
19
Q

What can Nifedipine, Nitrendipine and Nisoldipine do?

A

They are dihydropyridine calcium channel antagonists which can bind to LTCC and block the channel preventing calcium influx.

20
Q

What happens in phase 3?

A
  • Small potassium current starts to activate towards the end of the plateau which begins repolarisation.
  • As the membrane becomes repolarised (due to efflux of potassium via normal potassium channels), the IK1 potassium channel switches back on (it turns off during depolarisation).
  • The IK1 current is large and flows during diastole -> it acts to stabilise the resting membrane potential and reduce risk of arrhythmia.
21
Q

Different action potential profiles in the heart

A
  • Different parts of the heart have different action potential shapes due to different ionic currents flowing due to expression of different ionic channels.
  • These graph shapes combined create the iconic PQRST shaped wave.
22
Q

What happens in phase 4 and 0?

A
  • Resting membrane potential is determined by K+ moving out of cells
  • Upstroke is determined by a large increase in membrane permeability to sodium
23
Q

Which channels are present in the SA node and why?

A
  • Most of the types of channels exist in the SA node cells with the exception of IK1.
  • The function of IK1 is to maintain a stable membrane potential so SA node cells do not have a stable membrane potential.
  • There is very little sodium influx into SA node cells, instead, the upstroke is caused by Ca2+ influx.
  • The SA node cells contain T-type Ca2+ Channels (TTCC) which activate at a more negative potential than LTCC.
  • The ITO (transient outward) current is very small.
  • The pacemaker current If is present.
24
Q

How does the pacemaker potential affect heart rate?

A
  • With sympathetic stimulation of the heart (e.g. adrenaline), it makes the pacemaker potential (the gradual upward slope before the -40mV line) steeper
  • This means threshold potential is reached more quickly
  • With parasympathetic stimulation (e.g. ACh) there is a decrease in the gradient of pacemaker potential
  • Takes longer for membrane potential to meet the threshold thus reducing heart rate.
  • This is how autonomic nervous system modulates heart rate.
25
Q

What are the four parts of the cardiac conduction system?

A
  • Sinoatrial Node (Located in the right atrium)
  • Inter-nodal Fibre Bundles
    (Conduct AP to AV-node at a greater velocity than ordinary atrial muscle?)
Atrioventricular Node
(Produces a delay of ~100ms)
Ventricular Bundles (bundle branches, purkinje fibres).
Bundle of His descends from AV-node and splits into two bundle branches made of Purkinje fibres 
Purkinje Fibres - conduct AP at around 6x the velocity ordinary cardiac muscle and penetrate 1/3rd distance into myocardial wall.
26
Q

How are impulses propagated between cells?

A

By using gap junctions which cluster at intercalated discs and have low resistance

27
Q

The basics of an ECG

A
  • When a wave of depolarisation moves towards the positive electrode, an upward deflection is detected.
  • When a wave is moving away from the positive electrode, a downward deflection is detected.
  • Repolarising waves have the opposite effect on the trace.
28
Q

How is the intrinsic heart rate modulated?

A

Increased parasympathetic stimulation of SA node decreases heart rate and increases sympathetic stimulation increases heart rate and strength of contraction. Vagus nerve and sympathetic nerves involved as well and cardioregulatory and vasomotor centres in medulla oblongata

29
Q

Where is the SA node located?

A

Lies just below the epicardial surface at the boundary between the right atrium and SVC.

30
Q

How are impulses propagated?

A

The propagation of the cardiac action potential is due to a combination of passive spread of current and the existence of a threshold. The spread of current excites neighbouring cells easily because the membrane resistance between cells is low due to gap junctions. Gap junction resistance determine the extent of current spread.

31
Q

Pathway of electrical conduction through the heart

A
SAN -> LA (via bachmann's bundle)
SAN -> AVN (via internodal branches)
AVN -> Bundle of His
BOH -> L and R bundle branch
L/R Bundle branch -> purkinje fibres
32
Q

What is the pacemaker potential?

A

The slow, positive increase in voltage across the cell’s membrane at the start of the AP

33
Q

AP sequence in the SAN

A

Permeability to sodium increases so shallow upward stroke, then permeability to calcium so rapid upstroke, inactivation of calcium channels and then potassium channels open causing a downward stroke and then potassium channels close

34
Q

What is a graded potential?

A

Change in amplitude, can be bi-directional
Found at synapse and sensory receptors - if leads to an AP then called a generator potential
They decrease in amplitude over time and distance as charge leaks

35
Q

What is the function of a graded potential?

A

To generate or prevent AP

36
Q

What are the features of an AP and what is it preceded by?

A

uniform - all or nothing principle

preceded by generator potential