Cardiac Contractility and the Cardiac Cycle Flashcards
What is the purpose of cardiac T-tubule mucopolysaccharides?
To enrich the environment in favour of calcium influx
Explain contraction of cardiac muscle
- depolarisation travels across surface of cardiac muscle generated by SA node
- travels to T-tubules to open DHP, rush of influx of Ca, high plateau of stimulation causes a release of Ca from SR
- out floods Ca to interact with troponin which causes contraction
- amount of Ca released determines amount of force of contraction
Explain relaxation of cardiac muscle
2 ways:
- Ca can go back into SR in energy dependent ATP process
- can also be moved out by transporter which brings sodium in - this creates sodium current so Na K ATP-ase restores membrane potential by bringing potassium in
Explain how sympathetic innervation has a positive ionotropic effect on contraction
- enhances Ca influx
- promotes storage and release of Ca from SR
- increases contractility
- increases speed of relaxation
Explain how parasympathetic innervation has an indirect negative ionotropic effect
doesn’t directly affect contractility just indirectly allows the heart to relax for longer
- innervates atria
Explain why we cannot have summation or tetanaic contraction of cardiac activity
the plateau phase of contraction is driven by the calcium influx from DHP channels meaning that the AP extends almost as long as the contractile event its’s stimulating so by the time the cardiac AP is resolved, the muscle fibre is almost completely relaxed
Relative refractory period
if conditions are strong enough, another AP can be generated but highly unlikely
Supranormal excitability
lower than normal voltage change can open voltage gated Na channels
Revise cardiac cycle graph
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What is stroke volume (SV)?
- EDV-ESV
- quantity of blood expelled per beat
What is the cardiac output?
- SV x HR
- volume of blood pumped by the heart