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Aging Disrupts Normal Time-of-Day Variation in Cardiac Electrophysiology
Zhen Wang1, Srinivas Tapa1, Samantha D Francis Stuart1
1Department of Pharmacology, School of Medicine, University of California Davis (Z.W., S.T., S.D.F.S., L.W., J.B., C.M.R.).
Insights
Adult mouse hearts show significant daily variations in electrical activity and calcium handling, with reduced action potential duration at night. Aging disrupts these circadian patterns, impacting cardiac function and arrhythmia susceptibility.
Area of Science:
- Cardiovascular Physiology
- Chronobiology
- Molecular Cardiology
Background:
- Cardiac gene expression and arrhythmia occurrence exhibit daily variations.
- Daily changes in cardiac electrophysiology, arrhythmia susceptibility, and calcium handling remain poorly characterized.
- The impact of aging on these daily cardiac patterns is unknown.
Purpose of the Study:
- To characterize daily variations in cardiac electrophysiology, arrhythmia susceptibility, and calcium handling in adult mice.
- To investigate how aging affects these daily cardiac patterns.
- To assess the expression of key genes and proteins involved in cardiac function.
Main Methods:
- Isolated hearts from adult and aged male mice were Langendorff-perfused.
- Optical mapping with voltage- and calcium-sensitive dyes was used to assess electrophysiology.
- Real-time polymerase chain reaction and Western blot were employed to analyze gene and protein expression.
Main Results:
- Adult hearts displayed shortest action potential and calcium transient durations at ZT14 (night).
- Arrhythmia susceptibility and adrenergic responsiveness were diminished at ZT14 in adult hearts.
- Aged hearts showed minimal time-of-day variation in most assessed parameters, unlike adult hearts.
- Gene expression of KCNA5 increased, while ADRB1 decreased at ZT14 versus ZT4 in adult hearts.
Conclusions:
- Isolated adult hearts exhibit significant time-of-day variations in electrophysiology, calcium handling, and adrenergic responsiveness.
- Aging disrupts these circadian rhythms in cardiac function.
- These findings highlight the importance of considering daily rhythms in cardiovascular research and clinical practice.
Background:
Cardiac gene expression and arrhythmia occurrence have time-of-day variation; however, daily changes in cardiac electrophysiology, arrhythmia susceptibility, and Ca2+ handling have not been characterized. Furthermore, how these patterns change with age is unknown.
Methods:
Hearts were isolated during the light (zeitgeber time [ZT] 4 and ZT9) and dark cycle (ZT14 and ZT21) from adult (12-18 weeks) male mice. Hearts from aged (18-20 months) male mice were isolated at ZT4 and ZT14. All hearts were Langendorff-perfused for optical mapping with voltage- and Ca2+-sensitive dyes (n=4-7/group). Cardiac gene and protein expression were assessed with real-time polymerase chain reaction (n=4-6/group) and Western blot (n=3-4/group).
Results:
Adult hearts had the shortest action potential duration (APD) and Ca2+ transient duration (CaTD) at ZT14 (APD80: ZT4: 45.4±4.1 ms; ZT9: 45.1±8.6 ms; ZT14: 34.7±4.2 ms; ZT21: 49.2±7.6 ms, P<0.05 versus ZT4 and ZT21; and CaTD80: ZT4: 70.1±3.3 ms; ZT9: 72.7±2.7 ms; ZT14: 64.3±3.3 ms; ZT21: 74.4±1.2 ms, P<0.05 versus other time points). The pacing frequency at which CaT alternans emerged was faster, and average CaT alternans magnitude was significantly reduced at ZT14 compared with the other time points. There was a trend for decreased spontaneous premature ventricular complexes and pacing-induced ventricular arrhythmias at ZT14, and the hearts at ZT14 had diminished responses to isoproterenol compared with ZT4 (ZT4: 49.5.0±5.6% versus ZT14: 22.7±9.5% decrease in APD, P<0.01). In contrast, aged hearts exhibited no difference between ZT14 and ZT4 in nearly every parameter assessed (except APD80: ZT4: 39.7±1.9 ms versus ZT14: 33.8±3.1 ms, P<0.01). Gene expression of KCNA5 (potassium voltage-gated channel subfamily A member 5; encoding Kv1.5) was increased, whereas gene expression of ADRB1 (encoding β1-adrenergic receptors) was decreased at ZT14 versus ZT4 in adult hearts. No time-of-day changes in expression or phosphorylation of Ca2+ handling proteins (SERCA2 [sarco/endoplasmic reticulum Ca2+-ATPase], RyR2 [ryanodine receptor 2], and PLB [phospholamban]) was found in ex vivo perfused adult isolated hearts.
Conclusions:
Isolated adult hearts have strong time-of-day variation in cardiac electrophysiology, Ca2+ handling, and adrenergic responsiveness, which is disrupted with age.
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