· Intro
· Graph and conductance
· Pacemaker action potential
· Allows rapid, co-ordinated signalling · Rapid depolarisation followed by repolarization · Ion channels cycle through resting -> activated -> inactivated states |
|
Determinants of ion flux |
· Channel permeability: voltage dependent · Electrochemical gradients o Na+ and Ca2+ into cell, K+ out of cell o Mainly due to Na+K+ATPase |
(note: I have found it difficult to find consensus regarding voltages, channel opening times etc.; please advise me if you find a solid source)
Features |
· Automaticity o i.e. intrinsic, rhythmic, frequent depolaristion and contraction o HCN channel produces ‘funny current’ – i.e. mixed Na+ and K+ influx o [cAMP] ∝ If ∝ slope of phase 4 ∝ heart rate o Note depth of repolarisation ∝ IK ∝ 1/(heart rate) · Post-repolarisation refractoriness o RRP extends into phase 4 |
Refractory periods |
· ERP: insufficient HCN and Ca2+ channels resting; action potential (AP) impossible · RRP: enough HCN and Ca2+ channels resting but fewer than normal; AP possible with higher than normal stimulus |
Factors increasing rate |
· ↑SNS -> ↑If = ↑ICa > IK -> ↑steepness all slopes, especially phase 4 · ↑Temp -> ↑cell metabolic rate (enzymes, pumps) · ↓K+ -> less hyperpolarisation · Neonate: ↑resting HR (fixed stroke volume) |
Factors decreasing rate |
· ↑PSNS: -> ↓If, ↑IK -> ↓steepness phase 4, increased hyperpolarisation · ↓Temp -> ↓cell metabolic rate (enzymes, pumps) · Hypoxia -> failure of Na+K+ATPase, unable to repolarize cell, HCN not reactivated · Elderly: fibrous/fatty change in conduction system, ↓β1 adrenoceptors |
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