4.5 Article

Microvascular and capillary perfusion following glycocalyx degradation

Journal

JOURNAL OF APPLIED PHYSIOLOGY
Volume 102, Issue 6, Pages 2251-2259

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/japplphysiol.01155.2006

Keywords

functional capillary density; plasma volume; hyaluronan; capillary flow; red blood cell flux; tissue perfusion

Funding

  1. NHLBI NIH HHS [R01-HL76182] Funding Source: Medline
  2. PHS HHS [R01-62354, R01-62318, R24-64395] Funding Source: Medline

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Systemic parameters and microvascular and capillary hemodynamics were studied in the hamster window chamber model before and after hyaluronan degradation by intravenous injection of Streptomyces hyaluronidase (100 units, 40-50 U/ml plasma). Glycocalyx permeation was estimated using fluorescent markers of different molecular size (40, 70, and 2,000 kDa), and electrical charge. Systemic parameters (blood pressure, heart rate, blood gases) and microhemodynamics (vascular tone, velocity, and blood flow) remained statistically unchanged after injection of hyaluronidase. compared with inactivated hyaluronidase. Conversely. capillary hemodynamics were drastically affected. Functional capillary density. the capillaries perfused with red blood cells (RBCs), decreased by 35%, capillary Hct of the remaining functional capillaries increased from 16 to 27%, and penetration of 70-kDa fluorescent marker increased. Furthermore, plasma-only perfused capillaries statistically increased 30 min after hyaluronidase. The decrease in functional capillary density accounted for an increased RBC flux in the remainder of the capillaries, since the same number of RBCs had to traverse a reduced number of capillaries. Flux balances showed a reduction from baseline of 11% for the RBC flux and 20% for the plasma flux after treatment. These discrepancies are within the margin of error of the techniques used and could be explained by accounting for RBC over-velocity compared with plasma. These findings suggest that the decrease in the glycocalyx leads to capillary perfusion impairments.

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