cardiac muscle Flashcards
1
Q
properties of cardiac muscle
A
- Small cells (same as smooth)
- Striated (same as skeletal)
- Branched cells connected by intercalated discs
- Involuntary muscle
2
Q
does cardiac muscle have troponin
A
- yes
- Troponin is the calcium sensing protein
- In cardiac muscle, there are different isoforms of troponin (can distinguish between troponin in skeletal and cardiac muscle)
3
Q
does cardiac muscle have sarcomeres
A
yes
4
Q
are cardiac cells electrically coupled
A
yes
5
Q
3 components of intercalated discs
A
- interdigtating folds- in folds at the end of cells that increase the surface area of cell-cell connection
- mechanical junction-2 types: fascia adherens and desmosomes
- electrical junctions- electrically coupled by gap junctions. Enables each cell to stimulate the next
6
Q
gap junctions
A
- A hexamer composed of connexins provided by each cell
- Connexin = protein subunit that forms gap junctions
- Gap junctions hexamers (6 subunits) provided by adjacent cells form a gap junction with 12 subunits which connects the cells
- Present in intercalated discs
- low-resistance pathway between cells
- cell-cell conductance by electrical coupling
- Gap junction plaques - 5 to 500 gap junctions which offer low resistance pathways and cell to cell conduction
7
Q
description of blood supply in cardiac muscle
A
- Requires continuous supply of oxygen for mitochondria to be able to rapidly oxidise substrates and generate ATP
- Rich capillary supply - approx 1 capillary per fibre
- Short diffusion distances for oxygen and waste products and waste
8
Q
2 types of electrical activity
A
- pace maker potential
2. prolonged cardiac action potential
9
Q
3 ion conducting mechanisms
A
- Funny channel
- T-type calcium channels
- L-type calcium channels
10
Q
what is contraction in cardiac muscle cells in response to
A
- membrane action potential that propagates through the T-tubules
11
Q
L type Ca 2+ channels
A
- (long lasting current)
- Modified DHP receptors that act as the voltage sensor in skeletal muscle excitation-contraction coupling
- Enable depolarization of the cell due to influx of extracellular Ca2+
- VGCs
12
Q
Where does Ca2+ for contraction come from
A
- When L-type channels are open, there is an influx of calcium
- Calcium levels in cytoplasm increase
- Calcium regulates the activity of the ryanodine receptor
- ryanodine receptors on external surface of sarcoplasmic reticulum are Ca2+ channels, and not opened by voltage as in skeletal muscle, instead by binding of trigger Ca2+ in the cytosol
- Causes ryanodine receptor to open and release more calcium into the cytoplasm from the sarcoplasmic reticulum
- This binds to troponin
- Allows cross bridge cycling to occur
- Calcium is pumped back into the sarcoplasmic reticulum via a protein called serca
13
Q
Any differences between skeletal muscle filament activation, cross bridge cycling etc and in cardiac muscle
A
No
14
Q
when does contraction end
A
- when cytosolic Ca2+ concentration restores to its low value by Ca2+ ATPase pumps in the sarcoplasmic reticulum and sarcolemma (cell membrane of muscle cell)
15
Q
Sequence of excitation-contraction coupling
A
- Membrane depolarised by Na+ as an AP begins
- Depolarisation opens L-type channels in T tubules
- Trigger Ca2+ enters cytosol, contributing to cell depolarisation. Binds to and opens ryanodine receptor
- Ca2+ flows into cytosol, cross bridge cycling occurs
- Once Ca2+ has been restored to same level, membrane is repolarized when K+ exits the cell to end the action potential