Evidence map›Paper›PMID 21199399›Full record

ReviewActa physiologica (Oxford, England)2011

Dynamics of muscle microcirculatory and blood-myocyte O(2) flux during contractions.

D C Poole, S W Copp, D M Hirai, T I Musch

Open access · greenAbstract readReview
In one paragraph

Review in Acta physiologica (Oxford, England), 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing papers in PubMed
24.0field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

52 citing papers in PubMed, 100 citations in OpenAlex.

  1. Trial
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  3. Review
  4. Evidence that myoglobin PoFunction (Oxford, England) · 2026
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  6. KMicrovascular research · 2025
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  7. Frontiers in physiology · 2025
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  10. Review
  11. Review
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  14. Article
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  18. Regulation of capillary hemodynamics by KPhysiological reports · 2021
    Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

D C PooleDepartments of Kinesiology, Anatomy and Physiology, Kansas State University, Manhattan, KS, USA. poole@vet.ksu.edu
S W Copp
D M Hirai
T I Musch
Kansas State University · US

Funding

MUSCLE CAPILLARY GEOMETRY, FLOW, AND OXYGEN TRANSFERR01HL050306 · NHLBI · KANSAS STATE UNIVERSITY · PI POOLE, DAVID C · 1998 to 2001
$437k
Aging, Chronic Disease and Skeletal Muscle PerfusionR21AG019228 · NIA · KANSAS STATE UNIVERSITY · PI MUSCH, TIMOTHY I · 2001 to 2002
$437k
GEOMETRICAL MICROSTRUCTURE AND FUNCTION IN DIAPHRAGMR29HL050306 · NHLBI · UNIVERSITY OF CALIFORNIA SAN DIEGO · PI POOLE, DAVID C · 1994 to 1997
–
NHLBI NIH HHS HL-50306NHLBI NIH HHS R01 HL050306NIA NIH HHS AG-19228NIA NIH HHS R21 AG019228
6 · The paper itself

Abstract

The O(2) requirements of contracting skeletal muscle may increase 100-fold above rest. In 1919, August Krogh's brilliant insights recognized the capillary as the principal site for this increased blood-myocyte O(2) flux. Based on the premise that most capillaries did not sustain RBC flux at rest, Krogh proposed that capillary recruitment [i.e. initiation of red blood cell (RBC) flux in previously non-flowing capillaries] increased the capillary surface area available for O(2) flux and reduced mean capillary-to-mitochondrial diffusion distances. More modern experimental approaches reveal that most muscle capillaries may support RBC flux at rest. Thus, rather than contraction-induced capillary recruitment per se, increased RBC flux and haematocrit within already-flowing capillaries probably elevate perfusive and diffusive O(2) conductances and hence blood-myocyte O(2) flux. Additional surface area for O(2) exchange is recruited but, crucially, this may occur along the length of already-flowing capillaries (i.e. longitudinal recruitment). Today, the capillary is still considered the principal site for O(2) and substrate delivery to contracting skeletal muscle. Indeed, the presence of very low intramyocyte O(2) partial pressures (PO(2)s) and the absence of intramyocyte PO(2) gradients, whilst refuting the relevance of diffusion distances, place an even greater importance on capillary hemodynamics. This emergent picture calls for a paradigm-shift in our understanding of the function of capillaries by de-emphasizing de novo'capillary recruitment'. Diseases such as heart failure impair blood-myocyte O(2) flux, in part, by decreasing the proportion of RBC-flowing capillaries. Knowledge of capillary function in healthy muscle is requisite for identification of pathology and efficient design of therapeutic treatments.

Indexed as

AnimalsCapillariesErythrocytesExerciseHemodynamicsHumansMicrocirculationMuscle CellsMuscle ContractionMuscle, SkeletalOxygenPartial PressureOxygen

Identifiers

PMID21199399
PMCPMC3115447
OpenAlexW1492157034

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.