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Implications‐Enzymatic Degradation of the Endothelial Glycocalyx on the Microvascular Hemodynamics and the Arteriolar Red Cell Free Layer of the Rat Cremaster Muscle
Author(s) -
Jani Vivek P,
Yalcin Ozlem,
Johnson Paul C,
Cabrales Pedro
Publication year - 2018
Publication title -
the faseb journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.709
H-Index - 277
eISSN - 1530-6860
pISSN - 0892-6638
DOI - 10.1096/fasebj.2018.32.1_supplement.lb279
Subject(s) - glycocalyx , cremaster muscle , blood flow , chemistry , biophysics , hemodynamics , lumen (anatomy) , microcirculation , materials science , biology , biochemistry , medicine , microbiology and biotechnology
Background The endothelial glycocalyx is a complex network of glycoproteins, proteoglycans, and glycosaminoglycans; it lines the vascular endothelial cells facing the lumen of blood vessels forming the endothelial glycocalyx layer (EGL). Objective This study aims to investigate the microvascular hemodynamics implication of the EGL by quantifying changes in blood flow hydrodynamics post enzymatic degradation of the glycocalyx layer. Methods High‐speed intravital microscopy videos of small arteries (around 35 μm) of the rat cremaster muscle were recorded at various time points after enzymatic degradation of the EGL. The thickness of the cell free layer (CFL), blood flow velocity profiles, and volumetric flow rates were quantified. Hydrodynamic effects of the presence of the EGL were observed in the differences between the thickness of CFL in microvessels with an intact EGL and glass tubes of similar diameters. Results Maximal changes in the thickness of CFL were observed 40 min post enzymatic degradation of the EGL. Analysis of the frequency distribution of the thickness of CFL allows for estimation of the thickness of the endothelial surface layer (ESL), the plasma layer, and the glycocalyx. Peak flow, maximum velocity, and mean velocity were found to statistically increase by 24%, 27%, and 25%, respectively, after enzymatic degradation of the glycocalyx. The change in peak‐to‐peak maximum velocity and mean velocity were found to statistically increase by 39% and 32%, respectively, after 40 min post enzymatic degradation of the EGL. The bluntness of blood flow velocity profiles was found to be reduced post degradation of the EGL, as the exclusion volume occupied by the EGL increased the effective volume impermeable to RBCs in microvessels. Conclusion This study presents the effects of the EGL on microvascular hemodynamics. Enzymatic degradation of the EGL resulted in a decrease in the thickness of CFL, an increase in blood velocity, blood flow, and decrease of the bluntness of the blood flow velocity profile in small arterioles. In summary, the EGL functions as a molecular sieve to solute transport and as a lubrication layer to protect the endothelium from red blood cell (RBC) motion near the vessel wall, determining wall shear stress. Support or Funding Information This work was supported by NIH grants from the Heart Lung and Blood Institute, P01‐HL11090, R01HL126945, and R01‐ HL138116. This abstract is from the Experimental Biology 2018 Meeting. There is no full text article associated with this abstract published in The FASEB Journal .