| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1919694 | Mechanisms of Ageing and Development | 2007 | 8 Pages |
We investigated whether the age-related decrease in sensitivity of the heart to catecholamines was accompanied by changes in Ca2+ homeostasis and abnormal electrical and contractile activity caused by β-adrenergic receptor (β-AR) stimulation. Ventricular myocytes were isolated from young adult (3 months) and aged (24 months) male Fischer 344 rats. Unloaded cell shortening was measured in field-stimulated myocytes (2 Hz, 37 °C); membrane currents and action potentials were measured with microelectrodes. Contractile responses to the non-selective β-AR agonist, isoproterenol were significantly decreased in aged myocytes compared to younger myocytes and aged myocytes were less sensitive to isoproterenol. In contrast, Ca2+ transients measured simultaneously with contractions were similar between groups. Isoproterenol increased sarcoplasmic reticulum Ca2+ stores in both groups, but the increase was larger in aged cells. However, signs of Ca2+ overload induced by isoproterenol were reduced with age. Diastolic Ca2+ accumulation, contracture and the incidences of transient inward current, oscillatory afterpotentials (OAPs), aftertransients and aftercontractions induced by isoproterenol also were reduced with age. These results demonstrate that aged myocytes exhibit fewer signs of Ca2+ overload in response to isoproterenol than young adult myocytes. These age-related changes in intracellular Ca2+ may protect the aging heart against induction of arrhythmias initiated by OAPs.1
