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Bradykinin‐ and sodium nitroprusside‐induced increases in capillary tube haematocrit in mouse cremaster muscle are associated with impaired glycocalyx barrier properties
Author(s) -
VanTeeffelen Jurgen W. G. E.,
Constantinescu Alina A.,
Brands Judith,
Spaan Jos A. E.,
Vink Hans
Publication year - 2008
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1113/jphysiol.2008.152975
Subject(s) - glycocalyx , bradykinin , intravital microscopy , chemistry , sodium nitroprusside , medicine , endocrinology , perfusion , vasodilation , microcirculation , biochemistry , nitric oxide , receptor
Previous studies have suggested that agonists may increase functionally perfused capillary volume by modulation of blood‐excluding glycocalyx volume, but direct evidence for this association is lacking at the moment. Using intravital microscopic visualization of mouse cremaster muscle, we determined the effects of bradykinin (10 −5 m ) and sodium nitroprusside (10 −6 m ) on capillary tube haematocrit and glycocalyx barrier properties. In control C57Bl/6 mice ( n = 10), tube haematocrit in capillaries ( n = 71) increased ( P < 0.05) from 8.7 ± 0.3% during baseline to 21.2 ± 1.2 and 22.2 ± 0.9% during superfusion with bradykinin and nitroprusside, respectively. In parallel, the exclusion zone of FITC‐labelled 70 kDa dextrans decreased ( P < 0.05) from 0.37 ± 0.01 μm during baseline to 0.17 ± 0.01 μm with bradykinin and 0.15 ± 0.01 μm with nitroprusside. Bradykinin and nitroprusside had no effect on dextran exclusion and tube haematocrit in capillaries ( n = 55) of hyperlipidemic ApoE3‐Leiden mice, which showed impaired exclusion of 70 kDa dextrans (0.05 ± 0.02 μm; P < 0.05 versus C57Bl/6) and increased capillary tube haematocrit (23 ± 0.8%; P < 0.05 versus C57Bl/6) under baseline conditions, indicating glycocalyx degradation. Our data show that vasodilator substances increase functionally perfused capillary volume and that this effect is associated with a reduction in glycocalyx exclusion of 70 kDa dextrans. Modulation of glycocalyx volume might represent a novel mechanism of perfusion control at the capillary level.