HEME SYNTHESIS--EARLY DETECTION OF HEMOGLOBINOPATHIES
Project Number5R03DK050930-02
Contact PI/Project LeaderHIBBERT, JACQUELINE M
Awardee OrganizationVIRGINIA COMMONWEALTH UNIVERSITY
Description
Abstract Text
Many attempts have been made to obtain fundamental information about blood
diseases by estimating the life span of the red blood cell. While a number
of different clinical methods have been used, most are unreliable and none
is based on the direct measurement of hemoglobin synthesis rate. The
primary objective of this proposal is to develop an in vivo method to
enable measurement of the rate of fractional hemoglobin synthesis and red
blood cell life span, in hematologic diseases. The method has been adapted
from work described in the 1940's when hemoglobin was labeled with 15N-
glycine in vivo and the heme was isolated for analysis. The amino acid
glycine is required for the synthesis of the protoporphyrin of hemoglobin.
Progress in mass spectrometry analysis and the availability of 15N labels
now make such techniques feasible. Furthermore, it will be simple and more
affordable than the original method described. The secondary objective is
to apply this measurement to sickle cell disease, which provides a model
of changed red blood cell metabolism. Intermittent oral doses of 15N-
glycine, 400mg over 12 hours will label heme and globin. The heme is
ultimately lost in the stool as bilirubin and therefore this label will
not be recycled to heme synthesis. Blood will be collected at times zero
(pre dose), 12 and 24 hours, and the heme and globin will be isolated from
the red blood cell hemolysates. The intracellular free glycine pool will
be measured to represent the precursor pool enrichment for heme synthesis.
The glycine will be isolated with high performance liquid chromatography,
from a trichloroacetic acid extract of the red blood cell. Enrichments of
15N will be measured by mass spectrometry so that fractional hemoglobin
turnover rate and red blood cell survival time can be calculated. This
method will simultaneously measure rates of in vivo synthesis and
degradation of fetal and adult or sickle hemoglobin. The advantages of
this proposed method over the clinical use of chromium 51 (51 Cr) to tag
the red cells, are the accuracy and directness of the measurement.
Accuracy of the 51 Cr method is affected by leakage of chromium from the
red cell after the cells are removed from the subject, tagged in vitro and
then reintroduced to the subject. The tagged cells may also be
metabolically perturbed by this procedure. Finally, the proposed method
presents no radiation hazard and enables the dynamics of red cell
metabolism to be measured, as well as the estimates of red cell survival
time. In addition the procedure measures whole body protein turnover using
the 15N-glycine, urine collection and mass spectrometry. This can be
correlated with the fractional hemoglobin metabolism, to determine how
change in the metabolism of this one protein, is reflected in the whole
body. This method to measure the dynamics of hemoglobin metabolism will
have wide application as a tool for in vivo characterization of all
conditions resulting from altered hemoglobin synthesis. It may also
eventually prove useful in measuring platelet survival and turnover rates
as well as other blood constituents affected by disease.
National Institute of Diabetes and Digestive and Kidney Diseases
CFDA Code
DUNS Number
105300446
UEI
MLQFL4JSSAA9
Project Start Date
30-September-1995
Project End Date
31-August-1998
Budget Start Date
26-September-1996
Budget End Date
31-August-1998
Project Funding Information for 1996
Total Funding
$72,500
Direct Costs
$50,000
Indirect Costs
$22,500
Year
Funding IC
FY Total Cost by IC
1996
National Institute of Diabetes and Digestive and Kidney Diseases
$72,500
Year
Funding IC
FY Total Cost by IC
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