Electrical activity of the heart Flashcards
State the electrical properties of the heart
-
Excitation-contraction coupling in skeletal muscle VS cardiac muscle
SM- can exhibit tetanus ( good when carrying heavy weight)
-AP does not trigger opening of Ca2+ channels, but ttravels down T-tubules and causes release from Ca2+ from SR onl ( no extracellular)
CM - no tetanus ( need contraction and relaxation, otherwise no beating)
Longer action potential
- due to calcium entry delaying repolarisation of membranes. Calcium can come from cytosol/calcium dependent release from sacroplasmic reticulum.
Calcium does not saturate troponin like in skeletal muscle, so amount of calcium acts as a control
- Unstable MPs in pacemaker cells
- functional syncitium
Describe the features of the cardiac muscle ( e-c coupling)
- eletrically connected via gap junctions ( allows ions to pass depolarisation in neighbouring cells)
- physically connected by desmosones ( prevents cells from pulling apart during contraction)
- GJ + Des =intercelated discs
Why can’t cardiac muscle exhibit tetanus?
-long refractory period so no tetanic contraction
Describe the mechanism of Ca2+ in a muscle contraction
- regulation of calcium ions will regulate contraction ( can make contraction stronger/weaker depending on number). The more Ca2+, the more crossbridges will be formed.
- calcium release will not saturate all the troponin
- can regulate SV
Non-pacemaker ( mycocytes) action potential
RMP
-high resting PK+ (permeability - leaky K+ channels)
Initial depolarisation
- increase in PNa+ ( sodium voltage gated channels and they close quickly)
Plateau
- increase in PCa2+(L-type which lets in more Ca2+ vs T-type) - [opens slower but stays open longer]
- decrease in PK+
Repolarisation
- decrease in PCa2+ ( L-type)
- decrease in PK+
Pacemaker action potential
Action potential is slower due to:
-increase in PCa2+ ( L-type), only voltage gated Ca2+ NO Na+, hence slower.
Pacemaker potential
- there is a gradual decrease in PK+ (slow)
- BUT early increase in PNa+ ( = PF) [ voltage gated but different. Causes early AP due to Na+ flowing into cell via this funny channel]
- late increase in PCA2+ ( T-type) [ not big AP evoked due to less Ca2+ entering but threshold is still reached]
Pacemaker is autorythmicity ( self depolarising)
Modulators of electrical activity
-Drugs(anti-arrythmic), temperate, hconditions (hyperkalemia/calcemia hypokalemeria/calcemia )
Drugs
- Ca2+ channel blockers decrease in force of contraction[ L-type]. They operate by making less Ca2+ available to trigger cross-bridge formation.
- cardiac glycocides ( increases force of contraction) increased Ca2+ released from int stores so more crossbridge formation]
Temperature
- increase by 1 degree celcius = increase in HR by 10beats/min
Hyperkalemia ( high plasma K+)
- fibrilation + heart block [depolarises cells due to reduced conc gradient for K+ changing eq/potential + RMP. Cardiac cells more likely to fire..unordinated firing+contraction=fib]
- Heart block: If cells depolarise, smaller ion gradient pushing ions in + things happen slower to the point heart stops.
Hypokalemia
- fibrilation + heart block (anomalous) [ hyperpolarises but then depolarises]
Hypercalcemia
-increased HR + force of contraction
Hypocalcemia
-decreased HR + force of contraction
Name the Conduction system
- SA node ( pacemaker) [ self depolarises wheras cardiac cells depolarise due to neighbouring cell ]
- Annulus fibrosus ( non conducting) [ conduction stops here + NO GAP J]
- AV node ( delay box)
- Bundle of His
- Purkinje fibres ( rapid conduction system)
Describe the mechanism of the conduction system
An action potential in a single myocyte evokes a small extracellular electrical potential
- lots of small extracellular eletrical potentials are evoked by many cells depolarising and repolarising at the same time and can summate to creat a llarge extracellylar eletrical waves
- This is recorded at the periphery as the electrocardiogram
Describe the PQRST wave
P wave = atrial depolarisation
QRS complex = ventricular depolarisation
T wave = ventricular repolarisation
How is the cardiac muscle classified as a functional syncitium?
- this is formed by fusion of many cells, so many of these cells will operate as the 1 cell
- physically and electrically connected
Types of calcium ion channels
L type: allows large amount of Ca2+ ions into cell
T type: present in pacemaker cells and allows small amount of ions into cell over a long period
Funny current
-pacemaker potential is stange, sodium channels are opened up by repolarisation from previous AP