Document Detail


Design of the oxygen and substrate pathways. V. Structural basis of vascular substrate supply to muscle cells.
MedLine Citation:
PMID:  8708575     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
This paper quantifies the structural capacity of the transport steps for oxygen, glucose and fatty acids from the blood in capillaries to the cytosol of muscle cells and compares it with maximal rates of oxygen and substrate transport measured in the same animals and reported in the preceding papers of this series. Dogs have relatively more muscle per unit body mass than goats (37 versus 26%), but the maximal rate of oxidation per gram of muscle is still larger in the dog by a factor of 1.55. The maximal rates of substrate supply from the circulation are similar in both species. We predict that these differences in physiological parameters should be matched by proportional differences in structural capacity. We find that capillary volume and surface area are matched to maximal oxygen demand. The rate of vascular substrate supply is proportional neither to the capillary surface area nor to the length of intercellular junctions. The sarcolemmal surface area per gram of muscle is the same in both species. Using the physiological data presented in the companion papers of this series, we have calculated the maximal flux densities of circulatory glucose and fatty acids across the capillary wall and the sarcolemma. We find, for both substrates, that the flux densities across the sarcolemma reach a maximum at nearly the same level and at low exercise intensities in both species. In contrast, the flux densities across the capillary surface and the endothelial junctions are higher in goats than in dogs. We conclude that the capillaries are designed for O2 supply up to maximal rates of oxidation but not for the supply of the substrates (glucose and fatty acids) at the rates required at high exercise intensities. These are limited by the transport capacities of the sarcolemma.
Authors:
R Vock; E R Weibel; H Hoppeler; G Ordway; J M Weber; C R Taylor
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Publication Detail:
Type:  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.    
Journal Detail:
Title:  The Journal of experimental biology     Volume:  199     ISSN:  0022-0949     ISO Abbreviation:  J. Exp. Biol.     Publication Date:  1996 Aug 
Date Detail:
Created Date:  1996-09-12     Completed Date:  1996-09-12     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  0243705     Medline TA:  J Exp Biol     Country:  ENGLAND    
Other Details:
Languages:  eng     Pagination:  1675-88     Citation Subset:  IM    
Affiliation:
Department of Anatomy, University of Berne, Switzerland.
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MeSH Terms
Descriptor/Qualifier:
Animals
Biological Transport
Blood Glucose / metabolism*
Capillaries / ultrastructure
Cytosol / metabolism
Dogs
Endothelium, Vascular / metabolism,  ultrastructure
Fatty Acids / metabolism*
Female
Goats
Intercellular Junctions / metabolism
Kinetics
Microscopy, Electron
Muscle, Skeletal / blood supply*,  ultrastructure*
Oxidation-Reduction
Oxygen Consumption*
Sarcolemma / metabolism
Grant Support
ID/Acronym/Agency:
AR 18140/AR/NIAMS NIH HHS
Chemical
Reg. No./Substance:
0/Blood Glucose; 0/Fatty Acids

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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