Literature DB >> 9167209

Circulating red cell volume and red cell survival can be accurately determined in sheep using the [14C]cyanate label.

D M Mock1, G L Lankford, L F Burmeister, R G Strauss.   

Abstract

The sheep commonly serves as an animal model for investigation of human fetal and newborn erythropoiesis and red blood cell kinetics. Measurement of red cell volume (RCV) and survival (RCS) in sheep would be useful for studying mechanisms of neonatal anemia. Unfortunately 51Cr, the standard method for RCV, is not suitable for RCS in sheep because 51Cr leaves the red cell too rapidly. We developed and validated the permanent label [14C]cyanate as a method for measuring both RCV and RCS in sheep. In 19 sheep, RCV was determined simultaneously using [14C]cyanate and 51Cr. RCV determined by [14C]cyanate agreed almost perfectly with RCV by 51Cr; correlation coefficient = 0.990. The line of regression had a slope of 0.94 and an intercept of 40; these parameters are not significantly different from a line of identity. In nine sheep, RCS was determined using [14C]cyanate. Survival after d 1 accurately fit a model containing two components: 1) an early exponential loss likely related to damage caused by labeling and handling and 2) a linear decrease that reflected normal survival of undamaged red cells. Mean potential life span (MPL) determined from the linear phase was 114 +/- 12 d (mean +/- 1 SD). These results agree with reported MPL values determined either by 59Fe or differential hemolysis. Together, these observations establish [14C]cyanate-labeled red cells as a tool for measuring both RCV and RCS in sheep and enhance the value of the ovine model for investigating neonatal anemia.

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Year:  1997        PMID: 9167209     DOI: 10.1203/00006450-199706000-00020

Source DB:  PubMed          Journal:  Pediatr Res        ISSN: 0031-3998            Impact factor:   3.756


  12 in total

1.  Red blood cell (RBC) volume can be independently determined in vivo in the sheep using ovine RBCs labeled at different densities of biotin.

Authors:  Donald M Mock; Nell I Matthews; Shan Zhu; Leon F Burmeister; M Bridget Zimmerman; Ronald G Strauss; Robert L Schmidt; Demet Nalbant; Kevin J Freise; Peter Veng-Pedersen; John A Widness
Journal:  Transfusion       Date:  2010-12       Impact factor: 3.157

2.  Receptor-based dosing optimization of erythropoietin in juvenile sheep after phlebotomy.

Authors:  Matthew Rosebraugh; John A Widness; Peter Veng-Pedersen
Journal:  Drug Metab Dispos       Date:  2011-04-01       Impact factor: 3.922

3.  Comparison of red blood cell survival in sheep determined using red blood cells labeled with either biotin at multiple densities or [14C]cyanate: validation of a model to study human physiology and disease.

Authors:  Donald M Mock; Nell I Matthews; Shan Zhu; Ronald G Strauss; Robert L Schmidt; M Bridget Zimmerman; Demet Nalbant; Kevin J Freise; Mohammad Saleh; Peter Veng-Pedersen; John A Widness
Journal:  Transfusion       Date:  2012-01-09       Impact factor: 3.157

4.  Accelerated removal of antibody-coated red blood cells from the circulation is accurately tracked by a biotin label.

Authors:  Donald M Mock; Gary L Lankford; Nell I Matthews; Leon F Burmeister; Daniel Kahn; John A Widness; Ronald G Strauss
Journal:  Transfusion       Date:  2011-10-24       Impact factor: 3.157

5.  Red cell volume can be accurately determined in sheep using a nonradioactive biotin label.

Authors:  Donald M Mock; Nell I Mock; Gary L Lankford; Leon F Burmeister; Ronald G Strauss; John A Widness
Journal:  Pediatr Res       Date:  2008-11       Impact factor: 3.756

6.  Red blood cell volume can be independently determined in vitro using sheep and human red blood cells labeled at different densities of biotin.

Authors:  Donald M Mock; Nell I Matthews; Ronald G Strauss; Leon F Burmeister; Robert Schmidt; John A Widness
Journal:  Transfusion       Date:  2009-02-10       Impact factor: 3.157

7.  Pharmacodynamic modeling of the effect of changes in the environment on cellular lifespan and cellular response.

Authors:  Kevin J Freise; Robert L Schmidt; John A Widness; Peter Veng-Pedersen
Journal:  J Pharmacokinet Pharmacodyn       Date:  2008-10-21       Impact factor: 2.745

8.  Pharmacodynamic analysis of time-variant cellular disposition: reticulocyte disposition changes in phlebotomized sheep.

Authors:  Kevin J Freise; John A Widness; Robert L Schmidt; Peter Veng-Pedersen
Journal:  J Pharmacokinet Pharmacodyn       Date:  2007-05-22       Impact factor: 2.745

9.  Posttransfusion 24-hour recovery and subsequent survival of allogeneic red blood cells in the bloodstream of newborn infants.

Authors:  Ronald G Strauss; Donald M Mock; John A Widness; Karen Johnson; Gretchen Cress; Robert L Schmidt
Journal:  Transfusion       Date:  2004-06       Impact factor: 3.157

10.  Is it possible to predict the blood volume of a sick preterm infant?

Authors:  N Aladangady; T C Aitchison; C Beckett; B M Holland; B M Kyle; C A J Wardrop
Journal:  Arch Dis Child Fetal Neonatal Ed       Date:  2004-07       Impact factor: 5.747

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