HEPARINASE TREATMENT SUGGESTS A ROLE FOR THE ENDOTHELIAL-CELL GLYCOCALYX IN REGULATION OF CAPILLARY HEMATOCRIT

HEPARINASE TREATMENT SUGGESTS A ROLE FOR THE ENDOTHELIAL-CELL GLYCOCALYX IN REGULATION OF CAPILLARY HEMATOCRIT
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DOI:
10.1152/ajpheart.1990.258.3.h647
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发表时间:
1990-03-01
影响因子:
--
通讯作者:
DULING, BR
DULING, BR
中科院分区:
其他
文献类型:
--
作者:
DESJARDINS, C;DULING, BR

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Physiological stimuli induce rapid and unexplained increases in the number of red blood cells within capillaries of skeletal muscle. We hypothesized that such alterations in intracapillary red cell numbers might be due to an undefined interaction between one or more components of blood and the luminal surface of the capillary. This proposition was tested by in situ microperfusion of capillaries with enzymes directed against macromolecules likely to be expressed on the surface of endothelial cells. The instantaneous fractional volume of red blood cells within a capillary (tube hematocrit) was used as an index of a capillary''s response to enzyme microperfusion. Five to 8 min of perfusion with enzyme vehicle (0.25% albumin-Ringer solution) produced no significant alteration in capillary tube hematocrit. Perfusion with solutions containing heparinase raised the tube hematocrit at least twofold (P < 0.05) without a significant change in red cell velocity. Heat-denatured heparinase and other enzymes such as neuraminidase, hyaluronidase, papain, pronase E, and clostripain had no detectable effect on the tube hematocrit (P > 0.05). After enzyme treatment, appication of adneosine (10-4 M) or oxygen caused brisk vasomotor responses in arterioles feeding perfused capillary units, but the usual changes in the tube hematocrit were not observed. Thus heparinase treatment results in a sustained elevation in the capillary tube hematocrit and a dissociation of the typical relationship between vasomotor changes and red cell distribution in capillaries. These findings suggest that physiological stimuli which alter the number of red blood cells within capillaries may operate by modifying interactions between plasma and one or more components on the luminal surface of capillaries.