Literature DB >> 16339826

Cardiac vagal modulation of heart rate during prolonged submaximal exercise in animals with healed myocardial infarctions: effects of training.

Monica Kukielka1, Douglas R Seals, George E Billman.   

Abstract

The present study investigated the effects of long-duration exercise on heart rate variability [as a marker of cardiac vagal tone (VT)]. Heart rate variability (time series analysis) was measured in mongrel dogs (n = 24) with healed myocardial infarctions during 1 h of submaximal exercise (treadmill running at 6.4 km/h at 10% grade). Long-duration exercise provoked a significant (ANOVA, all P < 0.01, means +/- SD) increase in heart rate (1st min, 165.3 +/- 15.6 vs. last min, 197.5 +/- 21.5 beats/min) and significant reductions in high frequency (0.24 to 1.04 Hz) power (VT: 1st min, 3.7 +/- 1.5 vs. last min, 1.0 +/- 0.9 ln ms(2)), R-R interval range (1st min, 107.9 +/- 38.3 vs. last min, 28.8 +/- 13.2 ms), and R-R interval SD (1st min, 24.3 +/- 7.7 vs. last min 6.3 +/- 1.7 ms). Because endurance exercise training can increase cardiac vagal regulation, the studies were repeated after either a 10-wk exercise training (n = 9) or a 10-wk sedentary period (n = 7). After training was completed, long-duration exercise elicited smaller increases in heart rate (pretraining: 1st min, 156.0 +/- 13.8 vs. last min, 189.6 +/- 21.9 beats/min; and posttraining: 1st min, 149.8 +/- 14.6 vs. last min, 172.7 +/- 8.8 beats/min) and smaller reductions in heart rate variability (e.g., VT, pretraining: 1st min, 4.2 +/- 1.7 vs. last min, 0.9 +/- 1.1 ln ms(2); and posttraining: 1st min, 4.8 +/- 1.1 vs. last min, 2.0 +/- 0.6 ln ms(2)). The response to long-duration exercise did not change in the sedentary animals. Thus the heart rate increase that accompanies long-duration exercise results, at least in part, from reductions in cardiac vagal regulation. Furthermore, exercise training attenuated these exercise-induced reductions in heart rate variability, suggesting maintenance of a higher cardiac vagal activity during exercise in the trained state.

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Year:  2005        PMID: 16339826     DOI: 10.1152/ajpheart.01034.2005

Source DB:  PubMed          Journal:  Am J Physiol Heart Circ Physiol        ISSN: 0363-6135            Impact factor:   4.733


  7 in total

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Journal:  J Appl Physiol (1985)       Date:  2016-01-28

Review 2.  Translational neurocardiology: preclinical models and cardioneural integrative aspects.

Authors:  J L Ardell; M C Andresen; J A Armour; G E Billman; P-S Chen; R D Foreman; N Herring; D S O'Leary; H N Sabbah; H D Schultz; K Sunagawa; I H Zucker
Journal:  J Physiol       Date:  2016-06-17       Impact factor: 5.182

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Authors:  Monica Kukielka; Bethany J Holycross; George E Billman
Journal:  Front Physiol       Date:  2011-02-14       Impact factor: 4.566

Review 4.  Cardiac Autonomic Responses during Exercise and Post-exercise Recovery Using Heart Rate Variability and Systolic Time Intervals-A Review.

Authors:  Scott Michael; Kenneth S Graham; Glen M Davis
Journal:  Front Physiol       Date:  2017-05-29       Impact factor: 4.566

5.  Heart Rate Changes Before, During, and After Treadmill Walking Exercise in Normal Dogs.

Authors:  Sarah A Shull; Sarah K Rich; Robert L Gillette; Jane M Manfredi
Journal:  Front Vet Sci       Date:  2021-04-12

6.  Iyengar yoga increases cardiac parasympathetic nervous modulation among healthy yoga practitioners.

Authors:  Kerstin Khattab; Ahmed A Khattab; Jasmin Ortak; Gert Richardt; Hendrik Bonnemeier
Journal:  Evid Based Complement Alternat Med       Date:  2007-12       Impact factor: 2.629

7.  Monitoring training status with HR measures: do all roads lead to Rome?

Authors:  Martin Buchheit
Journal:  Front Physiol       Date:  2014-02-27       Impact factor: 4.566

  7 in total

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