Journal of Applied Physiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Appl Physiol 99: 505-514, 2005. First published March 31, 2005; doi:10.1152/japplphysiol.00896.2004
8750-7587/05 $8.00
This Article
Right arrow Full Text Free
Right arrow Full Text (PDF) Free
Right arrow All Versions of this Article:
99/2/505    most recent
00896.2004v1
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via ISI Web of Science (1)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Eklund, K. E.
Right arrow Articles by Musch, T. I.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Eklund, K. E.
Right arrow Articles by Musch, T. I.

Impact of aging on muscle blood flow in chronic heart failure

Kevin E. Eklund, K. Sue Hageman, David C. Poole, and Timothy I. Musch

Clarenburg Research Laboratory, Departments of Kinesiology, Anatomy and Physiology, Kansas State University, Manhattan, Kansas

Submitted 18 August 2004 ; accepted in final form 26 March 2005

Chronic heart failure (CHF) is manifested principally in the elderly population. Therefore, to understand the causes of exercise intolerance in CHF patients, it is imperative to resolve the effects of aging on muscle blood flow (BF) in CHF. To address this issue, we determined the muscle BF response to submaximal treadmill exercise (20 m/min, 5% grade) in young (YCHF: 6–8 mo, 412 ± 11 g, n = 11) and old (OCHF: 27–29 mo, 494 ± 10 g, n = 8) Fischer 344 x Brown Norway rats with similar degrees of myocardial infarction-induced left ventricular (LV) dysfunction [resting LV end-diastolic pressure: YCHF = 24 ± 2, OCHF = 22 ± 2 mmHg; derivative of LV pressure over time: YCHF = 5,168 ± 285; OCHF = 5,050 ± 165 mmHg/s; lung weight normalized to body weight: YCHF = 9.14 ± 0.72; OCHF = 8.21 ± 0.29 mg/g (all P > 0.05)]. The exercising heart rate response was blunted in OCHF compared with YCHF rats (YCHF = 454 ± 8, OCHF = 395 ± 9 beats/min; P < 0.05). BF (radiolabeled microspheres) to the total hindlimb musculature and to each of the 28 individual muscles examined was similar between YCHF and OCHF rats under resting conditions. During exercise, BF to five of the hindlimb muscles that normally possess a majority of slow-twitch oxidative and fast-twitch oxidative glycolytic muscle fibers increased significantly less (–25 to –42%) for OCHF compared with YCHF rats. In contrast, BF to 14 of the hindlimb muscles that normally possess a majority of fast-twitch glycolytic muscle fibers was increased (+22 to +337%) for OCHF vs. YCHF rats, which contributed to a greater mass-specific total hindlimb BF response in OCHF rats (YCHF = 78 ± 5, OCHF = 100 ± 11 ml·min–1·100 g–1; P < 0.05) and coincided with greater reductions in BF to the kidneys and splanchnic organs during exercise in OCHF vs. YCHF. In conclusion, there appears to be a profound age-related redistribution of BF from the highly oxidative to the highly glycolytic muscles of the hindlimb during exercise in OCHF compared with YCHF rats. This phenomenon is qualitatively similar to that reported previously for healthy young and old rats.

myocardial infarction; exercise; fiber type; left ventricular dysfunction; exercise hyperemia



Address for reprint requests and other correspondence: T. I. Musch, Dept. of Anatomy and Physiology, College of Veterinary Medicine, 128 Coles Hall, 1600 Denison Ave., Manhattan, KS 66505-5802 (E-mail: musch{at}vet.ksu.edu)







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2005 by the American Physiological Society.