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Journal of applied physiology (Bethesda, Md. : 1985)1992; 73(6); 2274-2282; doi: 10.1152/jappl.1992.73.6.2274

O2 delivery at VO2max and oxidative capacity in muscles of standardbred horses.

Abstract: The purpose of this study was to describe the relationships between 16 physiological, biochemical, and morphological variables presumed to relate to the oxidative capacity in quadriceps muscles or muscle parts in Standardbred horses. The variables included O2 delivery (blood flow) and mean capillary transit time (MTT) during treadmill locomotion at whole animal maximal O2 consumption (VO2max, 134 +/- 2 ml.min-1 x kg-1), capillary density and capillary-to-fiber ratio, myoglobin concentration, oxidative enzyme activities, glycolytic enzyme activities, fiber type populations, and fiber size. These components of muscle metabolic capacity were found to be interrelated to varying degrees using correlation matrix analysis, with lactate dehydrogenase activity showing the most significant correlations (n = 14) with other variables. Most of the "oxidative" variables occurred in the highest quantities in the deepest muscle of the group (vastus intermedius) and in the deepest parts of the other quadriceps muscles where the highest proportions of type I fibers were localized. The highest blood flow measured with microspheres in the muscle group during exercise was in vastus intermedius muscle (145 ml.min-1 x 100 g-1), and the lowest was in the superficial part of rectus femoris muscle (32 ml.min-1 x 100 g-1). Average muscle blood flow during exercise at whole animal VO2max was 116 ml.min-1 x 100 g-1. Because skeletal muscle comprised 43% of total body mass (453 +/- 34 kg), total muscle blood flow was estimated at 226 l/min, which was approximately 78% of total cardiac output (288 l/min).(ABSTRACT TRUNCATED AT 250 WORDS)
Publication Date: 1992-12-01 PubMed ID: 1337073DOI: 10.1152/jappl.1992.73.6.2274Google Scholar: Lookup
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  • Journal Article
  • Research Support
  • Non-U.S. Gov't
  • Research Support
  • U.S. Gov't
  • Non-P.H.S.
  • Research Support
  • U.S. Gov't
  • P.H.S.

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research article examines the relationship between multiple physiological, biochemical, and morphological factors theorized to be involved in the oxidative capacity of Standardbred horses’ quadriceps muscles. Notably, these factors include oxygen delivery, capillary density, and muscle fiber type distribution.

Understanding Oxidative Capacity and Variables

  • The study focuses on understanding the complex network of factors that correlate with and potentially impact the oxidative capacity in quadriceps muscle sections of Standardbred horses.
  • The researchers considered 16 key variables, including oxygen delivery, the mean capillary transit time during treadmill exercise at the animal’s maximal oxygen consumption,myoglobin concentration, and various enzyme activities.
  • The properties and activities of various enzyme types, fiber populations, and fiber sizes also play a role in this investigation.

Correlations Found

  • The researchers found that these aspects of muscle metabolic capacity were interconnected to varying extents, as shown by correlation matrix analysis.
  • Among all the variables, lactate dehydrogenase activity exhibited the most significant correlations with other aspects.

Relevance of Muscle Depth and Fiber Type

  • The study revealed that the highest quantities of “oxidative” variables were present in the deeper muscles of the quadriceps group (vastus intermedius), as well as in the deeper sections of other quadriceps muscles where type I fibers were predominantly located.
  • This suggests the vital role of muscle depth and fiber type in determining oxidative capacity.

Importance of Blood Flow

  • In terms of blood flow, highest rates were recorded in the vastus intermedius muscle during exercise, while the lowest were detected in the superficial part of the rectus femoris muscle.
  • This indicates how blood flow, and therefore presumably oxygen delivery, can significantly vary within different regions of the same muscle group.
  • The research also highlighted the importance of blood flow in terms of cardiac output, with the muscles taking approximately 78% of total cardiac output, underlining the significant cardiovascular demands of equine locomotion.

Cite This Article

APA
Armstrong RB, Essén-Gustavsson B, Hoppeler H, Jones JH, Kayar SR, Laughlin MH, Lindholm A, Longworth KE, Taylor CR, Weibel ER. (1992). O2 delivery at VO2max and oxidative capacity in muscles of standardbred horses. J Appl Physiol (1985), 73(6), 2274-2282. https://doi.org/10.1152/jappl.1992.73.6.2274

Publication

ISSN: 8750-7587
NlmUniqueID: 8502536
Country: United States
Language: English
Volume: 73
Issue: 6
Pages: 2274-2282

Researcher Affiliations

Armstrong, R B
  • Muscle Biology Laboratory, University of Georgia, Athens 30602.
Essén-Gustavsson, B
    Hoppeler, H
      Jones, J H
        Kayar, S R
          Laughlin, M H
            Lindholm, A
              Longworth, K E
                Taylor, C R
                  Weibel, E R

                    MeSH Terms

                    • Animals
                    • Capillaries / physiology
                    • Cardiac Output / physiology
                    • Electron Transport Complex IV / metabolism
                    • Female
                    • Glycolysis / physiology
                    • Horses
                    • L-Lactate Dehydrogenase / metabolism
                    • Male
                    • Microspheres
                    • Muscles / cytology
                    • Muscles / enzymology
                    • Muscles / metabolism
                    • Myoglobin / metabolism
                    • Oxidation-Reduction
                    • Oxygen Consumption / physiology

                    Grant Funding

                    • AM-37098 / NIADDK NIH HHS

                    Citations

                    This article has been cited 18 times.
                    1. Adepu KK, Anishkin A, Adams SH, Chintapalli SV. A versatile delivery vehicle for cellular oxygen and fuels or metabolic sensor? A review and perspective on the functions of myoglobin. Physiol Rev 2024 Oct 1;104(4):1611-1642.
                      doi: 10.1152/physrev.00031.2023pubmed: 38696337google scholar: lookup
                    2. Lyons SA, McClelland GB. Highland deer mice support increased thermogenesis in response to chronic cold hypoxia by shifting uptake of circulating fatty acids from muscles to brown adipose tissue. J Exp Biol 2024 Apr 1;227(7).
                      doi: 10.1242/jeb.247340pubmed: 38506250google scholar: lookup
                    3. Poole DC, Musch TI. Capillary-Mitochondrial Oxygen Transport in Muscle: Paradigm Shifts. Function (Oxf) 2023;4(3):zqad013.
                      doi: 10.1093/function/zqad013pubmed: 37168497google scholar: lookup
                    4. Araneda OF, Cavada G. Atmospheric Pollutants Affect Physical Performance: A Natural Experiment in Horse Racing Studied by Principal Component Analysis. Biology (Basel) 2022 Apr 30;11(5).
                      doi: 10.3390/biology11050687pubmed: 35625415google scholar: lookup
                    5. Schippers MP, Ramirez O, Arana M, McClelland GB. Increased Reliance on Carbohydrates for Aerobic Exercise in Highland Andean Leaf-Eared Mice, but Not in Highland Lima Leaf-Eared Mice. Metabolites 2021 Oct 29;11(11).
                      doi: 10.3390/metabo11110750pubmed: 34822408google scholar: lookup
                    6. Ono-Moore KD, Olfert IM, Rutkowsky JM, Chintapalli SV, Willis BJ, Blackburn ML, Williams DK, O'Reilly J, Tolentino T, Lloyd KCK, Adams SH. Metabolic physiology and skeletal muscle phenotypes in male and female myoglobin knockout mice. Am J Physiol Endocrinol Metab 2021 Jul 1;321(1):E63-E79.
                      doi: 10.1152/ajpendo.00624.2020pubmed: 33969704google scholar: lookup
                    7. Senefeld JW, Shepherd JRA, Baker SE, Joyner MJ. Sex-based limits to running speed in the human, horse and dog: The role of sexual dimorphisms. FASEB J 2021 May;35(5):e21562.
                      doi: 10.1096/fj.202100161Rpubmed: 33913189google scholar: lookup
                    8. Poole DC, Copp SW, Colburn TD, Craig JC, Allen DL, Sturek M, O'Leary DS, Zucker IH, Musch TI. Guidelines for animal exercise and training protocols for cardiovascular studies. Am J Physiol Heart Circ Physiol 2020 May 1;318(5):H1100-H1138.
                      doi: 10.1152/ajpheart.00697.2019pubmed: 32196357google scholar: lookup
                    9. Storz JF, Cheviron ZA, McClelland GB, Scott GR. Evolution of physiological performance capacities and environmental adaptation: insights from high-elevation deer mice (Peromyscus maniculatus). J Mammal 2019 May 23;100(3):910-922.
                      doi: 10.1093/jmammal/gyy173pubmed: 31138949google scholar: lookup
                    10. Joyner MJ, Casey DP. Regulation of increased blood flow (hyperemia) to muscles during exercise: a hierarchy of competing physiological needs. Physiol Rev 2015 Apr;95(2):549-601.
                      doi: 10.1152/physrev.00035.2013pubmed: 25834232google scholar: lookup
                    11. Castejón-Riber C, Muñoz A, Trigo P, Riber C, Santisteban R, Castejón F. Comparative ergoespirometric adaptations to a treadmill exercise test in untrained show Andalusian and Arabian horses. Vet Res Commun 2012 Mar;36(1):41-6.
                      doi: 10.1007/s11259-011-9510-xpubmed: 22183731google scholar: lookup
                    12. Kühl JT, Linde JJ, Fuchs A, Kristensen TS, Kelbæk H, George RT, Hove JD, Kofoed KF. Patterns of myocardial perfusion in humans evaluated with contrast-enhanced 320 multidetector computed tomography. Int J Cardiovasc Imaging 2012 Oct;28(7):1739-47.
                      doi: 10.1007/s10554-011-9986-zpubmed: 22143171google scholar: lookup
                    13. Williams CL, Meir JU, Ponganis PJ. What triggers the aerobic dive limit? Patterns of muscle oxygen depletion during dives of emperor penguins. J Exp Biol 2011 Jun 1;214(Pt 11):1802-12.
                      doi: 10.1242/jeb.052233pubmed: 21562166google scholar: lookup
                    14. Kanatous SB, Mammen PP, Rosenberg PB, Martin CM, White MD, Dimaio JM, Huang G, Muallem S, Garry DJ. Hypoxia reprograms calcium signaling and regulates myoglobin expression. Am J Physiol Cell Physiol 2009 Mar;296(3):C393-402.
                      doi: 10.1152/ajpcell.00428.2008pubmed: 19005161google scholar: lookup
                    15. Elder CP, Mahoney ET, Black CD, Slade JM, Dudley GA. Oxygen cost of dynamic or isometric exercise relative to recruited muscle mass. Dyn Med 2006 Sep 11;5:9.
                      doi: 10.1186/1476-5918-5-9pubmed: 16965630google scholar: lookup
                    16. Gorgey AS, Mahoney E, Kendall T, Dudley GA. Effects of neuromuscular electrical stimulation parameters on specific tension. Eur J Appl Physiol 2006 Aug;97(6):737-44.
                      doi: 10.1007/s00421-006-0232-7pubmed: 16821023google scholar: lookup
                    17. Kemper WF, Lindstedt SL, Hartzler LK, Hicks JW, Conley KE. Shaking up glycolysis: Sustained, high lactate flux during aerobic rattling. Proc Natl Acad Sci U S A 2001 Jan 16;98(2):723-8.
                      doi: 10.1073/pnas.98.2.723pubmed: 11120879google scholar: lookup
                    18. Kayar SR, Hoppeler H, Armstrong RB, Laughlin MH, Lindstedt SL, Jones JH, Conley KR, Taylor CR. Estimating transit time for capillary blood in selected muscles of exercising animals. Pflugers Arch 1992 Sep;421(6):578-84.
                      doi: 10.1007/BF00375054pubmed: 1437519google scholar: lookup