The impacts of age and frailty on heart rate and sinoatrial node function

被引:70
|
作者
Moghtadaei, Motahareh [1 ]
Jansen, Hailey J. [1 ]
Mackasey, Martin [1 ]
Rafferty, Sara A. [1 ]
Bogachev, Oleg [1 ]
Sapp, John L. [1 ,3 ]
Howlett, Susan E. [2 ]
Rose, Robert A. [1 ,4 ]
机构
[1] Dalhousie Univ, Fac Med, Dept Physiol & Biophys, Halifax, NS, Canada
[2] Dalhousie Univ, Dept Pharmacol, Fac Med, Halifax, NS, Canada
[3] Dalhousie Univ, Div Cardiol, Fac Med, Halifax, NS, Canada
[4] Dalhousie Univ, Sch Biomed Engn, Fac Med, Halifax, NS, Canada
来源
JOURNAL OF PHYSIOLOGY-LONDON | 2016年 / 594卷 / 23期
基金
加拿大健康研究院;
关键词
SICK SINUS SYNDROME; MATRIX METALLOPROTEINASES; DEFICIT ACCUMULATION; NATRIURETIC-PEPTIDE; PACEMAKER ACTIVITY; ELECTRICAL-CONDUCTION; ATRIAL-FIBRILLATION; MICE LACKING; ION-CHANNEL; FIBROSIS;
D O I
10.1113/JP272979
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Sinoatrial node (SAN) dysfunction increases with age, although not all older adults are affected in the same way. This is because people age at different rates and individuals of the same chronological age vary in health status from very fit to very frail. Our objective was to determine the impacts of age and frailty on heart rate (HR) and SAN function using a new model of frailty in ageing mice. Frailty, which was quantified in young and aged mice using a frailty index (FI), was greater in aged vs. young mice. Intracardiac electrophysiology demonstrated that HR was reduced whereas SAN recovery time (SNRT) was prolonged in aged mice; however, both parameters showed heteroscedasticity suggesting differences in health status among mice of similar chronological age. Consistent with this, HR and corrected SNRT were correlated with, and graded by, FI score. Optical mapping of the SAN demonstrated that conduction velocity (CV) was reduced in aged hearts in association with reductions in diastolic depolarization (DD) slope and action potential (AP) duration. In agreement with in vivo results, SAN CV, DD slope and AP durations all correlated with FI score. Finally, SAN dysfunction in aged mice was associated with increased interstitial fibrosis and alterations in expression of matrix metalloproteinases, which also correlated with frailty. These findings demonstrate that age-related SAN dysfunction occurs in association with electrical and structural remodelling and that frailty is a critical determinant of health status of similarly aged animals that correlates with changes in HR and SAN function.
引用
收藏
页码:7105 / 7126
页数:22
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