Document Detail


Effect of erythrocyte deformability on in vivo red cell transit time and hematocrit and their correlation with in vitro filterability.
MedLine Citation:
PMID:  8412852     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Indicator dilution techniques were applied to measure mean transit time of fluorescently labeled red blood cells (RBCs) (TTRBC) and plasma (TTpl) between functionally paired arterioles and venules (A-V) in cremaster muscle (rat) for normal RBCs and cells hardened by in vitro incubation in graded concentrations of glutaraldehyde. Dispersion of a bolus introduced into the contralateral femoral artery permitted computation of TT by cross-correlation of fluorescence intensity-time curves in A-V pairs. Parallel in vitro assessments of RBC deformability were made by filtration through 5-microns pore Nuclepore filters to express deformability in terms of the ratio of resistance to flow through a pore with RBCs present to that with suspending medium alone, beta. The average microvascular hematocrit (Hmicro) normalized with respect to systemic hematocrit (Hsys) was calculated from TTRBC and TTpl. For 26 A-V pairs of the third and fourth orders of branching, TTRBC averaged 0.63 sec for normal control cells (beta = 2.61), and TTpl averaged 0.85 sec with an average TTRBC/TTpl equal to 0.85. The corresponding value of Hmicro/Hsys was significantly < 1 and averaged 0.87. This greater value of Hmicro/Hsys compared to direct measurements in the literature was attributed to the unique ability of the indicator dilution technique to account for red cell flux throughout the network. For hardened RBCs with beta < 10, TTRBC/TTpl and Hmicro/Hsys increased on average 30%, but were weakly correlated with increasing beta due to redistribution of RBCs throughout pathways of lesser resistance. However, as beta rose from 10 to 20, these pathways became overwhelmed by hardened RBCs and TTRBC/TTpl increased threefold due to retardation of the RBC flux, with a concomitant rise in Hmicro/Hsys. These results clearly demonstrate the extent to which diminished RBC deformability of a magnitude found in clinical disorders may affect microvascular perfusion.
Authors:
H H Lipowsky; L E Cram; W Justice; M J Eppihimer
Publication Detail:
Type:  Comparative Study; In Vitro; Journal Article; Research Support, U.S. Gov't, P.H.S.    
Journal Detail:
Title:  Microvascular research     Volume:  46     ISSN:  0026-2862     ISO Abbreviation:  Microvasc. Res.     Publication Date:  1993 Jul 
Date Detail:
Created Date:  1993-10-28     Completed Date:  1993-10-28     Revised Date:  2007-11-14    
Medline Journal Info:
Nlm Unique ID:  0165035     Medline TA:  Microvasc Res     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  43-64     Citation Subset:  IM    
Affiliation:
Bioengineering Program, Penn State University, University Park 16802.
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MeSH Terms
Descriptor/Qualifier:
Animals
Erythrocyte Deformability / physiology*
Erythrocytes / cytology*
Filtration
Hematocrit
Male
Oxygen / blood
Perfusion
Rats
Rats, Sprague-Dawley
Time Factors
Grant Support
ID/Acronym/Agency:
HL-28381/HL/NHLBI NIH HHS; HL-39286/HL/NHLBI NIH HHS
Chemical
Reg. No./Substance:
7782-44-7/Oxygen

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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