Faculty Collaboration Database

Effects of regular exercise on ventricular myocyte biomechanics and K_ATP channel function. Am J Physiol Heart Circ Physiol 2018 Oct 01;315(4):H885-H896

Date

08/04/2018

Pubmed ID

30074836

DOI

10.1152/ajpheart.00130.2018

Scopus ID

2-s2.0-85053835914 (requires institutional sign-in at Scopus site)   9 Citations

Abstract

Exercise training is known to protect the heart from ischemia and improve function during exercise by reducing cardiomyocyte action potential duration (APD) and increasing contractility. The cellular mechanisms involve β-adrenergic regulation and the ATP-sensitive K⁺ (K_ATP) channel, but how each alters function of the left ventricle and sex specificity is unknown. To address this, female and male Sprague-Dawley rats were randomly assigned to wheel-running (TRN) or sedentary (SED) groups. After 6-8 wk of training, myocytes were isolated from the left ventricle and field stimulated at 1, 2, and 5 Hz. TRN significantly increased cardiomyocyte contractility, the kinetics of the Ca²⁺ transient, and responsiveness to the adrenergic receptor agonist isoproterenol (ISO), as reflected by an increased sarcomere shortening. Importantly, we demonstrated a TRN-induced upregulation of K_ATP channels, which was reflected by elevated content, current density, and the channel's contribution to APD shortening at high activation rates and in the presence of the activator pinacidil. TRN induced increase in K_ATP current occurred throughout the left ventricle, but channel subunit content showed regional specificity with increases in Kir6.2 in the apex and SUR2A in base regions. In summary, TRN elevated cardiomyocyte cross-bridge kinetics, Ca²⁺ sensitivity, and the responsiveness of contractile function to β-adrenergic receptor stimulation in both sexes. Importantly, upregulation of the K_ATP channel accelerates repolarization and shortens APD during stress and exercise. These adaptations have clinical importance, as increased contractility and reduced APD would help protect cardiac output and reduce intracellular Ca²⁺ overload during stresses such as regional ischemia. NEW & NOTEWORTHY Our results demonstrate that regular exercise significantly increased ventricular myocyte shortening and relaxation velocity and the rate of rise in intracellular Ca²⁺ transient and enhanced the response of biomechanics and Ca²⁺ reuptake to β-adrenergic stimulation. Importantly, exercise training upregulated the cardiomyocyte sarcolemma ATP-sensitive K⁺ channel across the left ventricle in both sexes, as reflected by elevated channel subunit content, current density, and the channel's contribution to reduced action potential duration at high activation rates.

Author List

Wang X, Fitts RH

Authors

Robert Fitts PhD Professor in the Biological Sciences department at Marquette University
Xinrui Wang Assistant Professor in the Pharmacology and Toxicology department at Medical College of Wisconsin

MESH terms used to index this publication - Major topics in bold

Adrenergic beta-Agonists
Animals
Biomechanical Phenomena
Calcium Signaling
Cardiac Pacing, Artificial
Female
Heart Ventricles
Isoproterenol
KATP Channels
Kinetics
Male
Myocardial Contraction
Myocytes, Cardiac
Physical Conditioning, Animal
Physical Exertion
Potassium Channels, Inwardly Rectifying
Rats, Sprague-Dawley
Sarcomeres
Sex Factors
Sulfonylurea Receptors
Ventricular Function, Left