Age reduces key calcium-handling proteins in rat sinoatrial node, lowering intrinsic pacemaker rate by 68 bpm and altering drug responses; NCX protein rose 57%.
Male Han Wistar rats used as a model of ageing throughout their lifespan at 6, 12 and 24 months of age
Ageing (evaluated at 6, 12, and 24 months) and pharmacological modulation of calcium handling (cyclopiazonic acid, nifedipine, isoprenaline)
Young rats (6 months of age)
Levels of key calcium regulatory proteins (Cav1.2, PMCA4, RYR2, SERCA2a, phospholamban, NCX) and intrinsic pacemaker beating ratesurrogate
Age-dependent reduction in sinoatrial node function is driven by a decline in sarcoplasmic reticulum calcium cycling proteins, which can be mimicked in young animals by blocking SR calcium handling.
Absolute Event Rate: 0% vs 0%
With advancing age, the intrinsic function of the sinoatrial node (SAN) declines, as a result of structural changes and changes in electrical regulation within the constitutive cells of the nodal tissue. This study examined changes to proteins involved in regulating calcium flux balance in the atria and SAN of male rats used as a model of ageing throughout their lifespan at 6, 12 and 24 months of age. Using immunohistochemistry and western blotting, we determined a significant age-dependent decline in the levels of key calcium regulatory proteins within the SAN: Cav1.2, PMCA4, RYR2, SERCA2a and phospholamban (n = 5; ANOVA, P -1 in the oldest group compared to the youngest, (n = 6; ANOVA, P = 0.022). Negating sarcoplasmic reticulum calcium cycling and the 'calcium clock' using cyclopiazonic acid reduced the intrinsic pacemaker activity of the SAN in young animals to that observed in the oldest group. Under these conditions, spontaneous activity and the response of the SAN to isoprenaline became matched across all age groups. Restoring sarcoplasmic reticulum function to the SAN in the elderly may offer a route to combatting age-related suppression of function, although care should be taken in the use of calcium channel antagonists to avoid precipitating sick-sinus syndrome. KEY POINTS: This study adds understanding and characterisation of the age-dependent progressive reduction in sinoatrial node (SAN) function. We compared atria and the SAN across the lifespan of a Han Wistar rat model of ageing with animals studied at 6, 12 and 24 months of age. SAN tissue from old rats showed significantly reduced expression of key cellular calcium regulatory proteins compared to nodal tissue from young rats. The SAN from old rats exhibited a slowed intrinsic beating rate and an altered response to drugs that modulate cellular calcium handling. Eliminating sarcoplasmic reticulum calcium handling makes the SAN of a young animal mimic features of an aged animal.
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Jones et al. (Tue,) reported a other. Age reduces key calcium-handling proteins in rat sinoatrial node, lowering intrinsic pacemaker rate by 68 bpm and altering drug responses; NCX protein rose 57%.
synapsesocial.com/papers/69a135b0ed1d949a99abfc03 — DOI: https://doi.org/10.1113/jp290221
Sandra A. Jones
Hull York Medical School
F Godbeer
Hull York Medical School
Matthew K. Lancaster
Electrophysiology
University of Leeds
Hull York Medical School
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