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Bioengineering Program, The Pennsylvania State University, University Park, Pennsylvania 16802
The effect of
reduced red blood cell (RBC) deformability on microvessel recruitment
attendant to a reduction in tissue
PO2 was studied in rat cremaster
muscle using indicator-dilution techniques. Transit times (TT) of
fluorescently labeled RBCs
(TTRBC) and plasma (TTPl) between functionally
paired arterioles and venules were obtained from their dispersion
throughout the microvascular network. Changes in
PO2 were effected by superfusing the
tissue with Ringer solution deoxygenated to different levels.
Arteriolar blood flow (
) was measured with the
two-slit technique, and the vascular volume (V) occupied by RBCs and
plasma was computed from the product of
× TT
during bolus infusions of rat and less deformable human RBCs to obtain
VRBC and fluorescently labeled albumin to obtain VPl.
Measurements of TTRBC and
TTPl permitted computation of an
average flow-weighted tissue (microvascular) hematocrit
(HM) relative to systemic values
(HS). During
infusions of autologous rat RBCs,
and total V
increased threefold in response to hypoxia, whereas normalized RBC TT
(TTRBC/TTPl)
and normalized tissue hematocrit
(HM/HS)
did not show a significant trend, indicating an increase in the number
of pathways through which the RBCs can traverse the network because of
spatial recruitment of capillaries. In contrast, during infusions of
human RBCs,
TTRBC/TTPl and
HM/HS
decreased significantly in response to hypoxia. Although
exhibited an increase similar to that during
rat RBC infusions, VRBC exhibited
a smaller increase compared with
VPl, suggesting that reduced RBC
deformability leads to a redistribution of RBCs through larger-diameter
pathways within the network and exclusion of these RBCs from pathways
normally recruited during hypoxia. Hence, reduced RBC deformability may
adversely affect capillary recruitment and physiological mechanisms
that ensure adequate delivery of oxygen to tissue.
vascular volume; erythrocyte deformability; tissue hematocrit; microvascular perfusion; hypoxia; oxygen transport
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