Table 6.
Age range | Cardiomyocyte type | Key points | Citation |
| |||
<1–75 years | Right ventricular | Age-dependent increase in ICa density | Cohen and Lederer (1993) |
<1–75 years 1–8 years | Right atrial and ventricular Right ventricular |
Age-dependent decrease in calcium window current | Cohen and Lederer (1993); Pelzmann et al. (1998) |
<1–79 years | Right atria |
Age-dependent increase in ICa amplitude Lower basal L-type calcium current amplitude and increased expression of inhibitory G proteins is seen in infant atrial cells, compared with adults |
Tipparaju et al. (2004) |
<1–79 years | Right atria |
No age-dependent difference in ICa No evidence for age-related changes in ICa density, steady-state inactivation or recovery from inactivation |
Roca et al. (1996) |
<2 years <0–40 years |
Left and right ventricle Ventricular |
Age-dependent increase in calcium-handling proteins Age-dependent increase in NCX, SERCA, phospholamban and L-type calcium channel; age-dependent decrease in T-type calcium channel expression |
Wiegerinck et al. (2009); Qu et al. (2000) |
<1–4 years | Right atria |
Excitation-contraction coupling matures with postnatal age Slower Ca2+ upstroke velocity in infant cells is likely to be attributable to structural immaturity and inefficient coupling between calcium channels and ryanodine receptors |
Hatem et al. (1995) |
<1 year | Right atria |
Paediatric action potential waveform modulates excitation-contraction coupling Prolonged early repolarization in paediatric cells is correlated with increased dependence on trans-sarcolemmal Ca2+ influx for contraction |
Wagner et al. (2005) |
<2 years | Left and right ventricle |
Age-dependent increase in force-frequency relationship At faster frequencies, newborn ventricular muscle strips have less developed force compared with slightly older infant muscle strips; results are likely to be linked to developmental changes in protein expression |
Wiegerinck et al. (2009) |