Quantitative measurement of erythropoiesis in the dog

1960 ◽  
Vol 198 (1) ◽  
pp. 183-186 ◽  
Author(s):  
S. M. Weissman ◽  
T. A. Waldmann ◽  
N. I. Berlin

The quantitative measurement of erythropoiesis requires the simultaneous determination of total red cell volume, rate of production of red cells and the red cell life span. The total red cell volume was measured with autologous Cr51-labeled red cells, the rate of production of red cells from the rate of disappearance of radioiron from the plasma and uptake by red cells, the red cell life span with C14-labeled glycine and the apparent red cell survival T1/2 with Cr51. The average total red cell volume of the dogs studied was 38.6 cc/kg; the plasma radioiron T1/2 was 66 minutes; the red cell radio-iron uptake was 80%; the serum iron was 102 µg/100 cc, and the plasma volume calculated from the peripheral hematocrit and total red cell volume was 46 cc/kg, and from the extrapolation to t0 of the radioiron disappearance was 48 cc/kg. From these figures the plasma iron turnover was calculated to be 0.63 mg/kg/day and the red cell iron renewal rate 1.26%/day. The average red cell life span was 108 days; the average apparent T1/2 of Cr51 red cell survival was 24.3 days; the average elution rate of Cr51 was 1.77%/day.

1962 ◽  
Vol 203 (3) ◽  
pp. 401-403 ◽  
Author(s):  
M. J. Cline ◽  
T. A. Waldmann

The effect of environmental temperature on erythropoiesis and erythrocyte life span was studied in frogs maintained at 4 C or 24–26 C. The red cell incorporation of radioiron was used as an index of the rate of erythropoiesis and diisopropylfluorophosphate-P32 was used to measure red cell survival. The red cell life span in frogs kept at 24–26 C was approximately 200 days. The incorporation of Fe59 into circulating red cells during the first 10 days after isotope administration was significantly greater in frogs at 24–26 C than in frogs at 4 C. The peripheral hematocrit decreased in groups of frogs kept at 4 C during the period of observation. The inconstancy of the hematocrit and presumably of the total red cell volume did not permit any definite conclusions regarding the apparently longer erythrocyte life span at low environmental temperatures.


1957 ◽  
Vol 35 (1) ◽  
pp. 1171-1181
Author(s):  
L. G. Israels ◽  
A. Chutorian ◽  
G. E. Delory ◽  
Esther Israels

Sulphaemoglobinaemia was produced in rabbits by the injection of para-aminopropriophenone and calcium sulphide. The disappearance of this pigment from the blood was used as an index of red cell survival. Sulphaemoglobin disappeared in an exponential fashion, indicating a mean red cell life span of 36 days. The red cells were also tagged with Cr51, and this method of measuring erythrocyte life span yielded values strongly suggesting that sulphaemoglobin in the red cell impairs its viability and leads to random cell destruction. Under these conditions it would seem that the disappearance rate of sulphaemoglobin is not a true measure of red cell survival.


Blood ◽  
1963 ◽  
Vol 22 (4) ◽  
pp. 459-465 ◽  
Author(s):  
MARTIN J. CLINE ◽  
NATHANIEL I. BERLIN

Abstract DFP32 or Cr51 red cell survival studies were performed in 39 patients with hematologic disorders. In each case the erythrocyte life span was also determined using the C14-labeled glycine technic. Good agreement was found between the survival data obtained by the DFP32 and the glycine method. The red cell Cr51 T½ failed to reflect moderate shortening of red cell survival in a significant number of cases when a 25 day half-time was taken as the lower limit of normal. The occasional discrepancy between the erythrocyte life spans obtained with labeled glycine and the Cr51 halftime is probably the result of the limitations of the prevalent method of Cr51 data analysis and of the wide range of Cr51 elution rates in disease. Because of its simplicity and reliability, the DFP32 technics appears to be the method of choice for the determination of red cell survival.


Blood ◽  
1957 ◽  
Vol 12 (2) ◽  
pp. 147-164 ◽  
Author(s):  
NATHANIEL I. BERLIN ◽  
JOHN H. LAWRENCE ◽  
PAUL J. ELMLINGER

Abstract Since anemia or polycythemia can result only from a change in rate of formation of red cells or a change in the life span of the red cells, a determination of the total red cell volume, Fe59 studies to estimate the rate and site of production of red cells, and C14-labeled glycine or Fe59 studies to determine the life span of red cells permit a description of the pathogenesis of any alterations in the erythropoietic state. This has been of great value in clinical hematology from the stand-point of understanding the basic nature of the various diseases and, in particular, the selection of patients with unusual anemias possibly related to hypersplenism who might benefit from splenectomy. Splenic erythropoiesis can be easily differentiated from splenic red cell destruction. Since two of these methods—the determination of the blood volume and the Fe59 studies—are now possible in general commumnity hospitals and since modifications of the Fe59 method permit the determination of the life span of the red cell, adequate evaluation of the erythropoietic state is now possible in general hospitals.


1957 ◽  
Vol 35 (12) ◽  
pp. 1171-1181 ◽  
Author(s):  
L. G. Israels ◽  
A. Chutorian ◽  
G. E. Delory ◽  
Esther Israels

Sulphaemoglobinaemia was produced in rabbits by the injection of para-aminopropriophenone and calcium sulphide. The disappearance of this pigment from the blood was used as an index of red cell survival. Sulphaemoglobin disappeared in an exponential fashion, indicating a mean red cell life span of 36 days. The red cells were also tagged with Cr51, and this method of measuring erythrocyte life span yielded values strongly suggesting that sulphaemoglobin in the red cell impairs its viability and leads to random cell destruction. Under these conditions it would seem that the disappearance rate of sulphaemoglobin is not a true measure of red cell survival.


Blood ◽  
1976 ◽  
Vol 47 (3) ◽  
pp. 481-488 ◽  
Author(s):  
S Charache ◽  
R Dreyer ◽  
I Zimmerman ◽  
CK Hsu

Abstract Nitrogen mustard and nor-nitrogen mustard inhibit sickling, but the concentrations required would be associated with unacceptable toxicity if these agents were administered to patients. Red cells could be treated extracorporeally and infused back into donors, if the alkylating agent could be removed or inactivated, if the treatment per se did not significantly shorten red cell survival, and if viable alkylated lymphocytes could be eliminated from the treated blood. To estimate whether these conditions could be met in a clinical trial, red cells from four dogs were alkylated at 6-wk intervals. No toxic reactions were observed, although not all nor-nitrogen mustard was removed by the washing procedure. Red cell survival was shortened to about half that of control cells, using concentrations of alkylating agent which reduce sickling by 50%. Lymphocytes from treated blood could still exclude trypan blue, but could not be shown to circulate after reinfusion into donor dogs. If alkylating agents are used to treat patients' cells, inhibition of sickling may outweigh the shortening of red cell life span induced by the treatment; blood should probably be irradiated before infusion to avoid administration of alkylated and potentially mutated, but viable, lymphocytes.


1958 ◽  
Vol 195 (3) ◽  
pp. 628-630 ◽  
Author(s):  
L. Kraintz ◽  
J. de Boer ◽  
E. L. Smith ◽  
R. A. Huggins

Dogs anesthetized with morphine-pentobarbital were injected with Cr51-tagged red cells, and their mixing time in the general circulation and the spleen was compared. The necessary blood samples were taken and the spleens rapidly excised at 10, 20 or 30 minutes after the injection of the tagged red cells. When the data were grouped according to the size of the spleen and irrespective of the time of removal, the mixing of tagged red cells in small spleens was practically the same as in the general circulation. With increasing sizes of spleens the mixing appeared to be progressively less complete than in the general circulation. If the spleen size was disregarded and the data grouped according to the time after the injections of tagged red cells mixing in the spleen was still incomplete after 30 minutes. However, the maximum mean possible error that could be introduced into the determination of total red cell volume if all the unmixed red cells were ejected into the general circulation would be less than 5% at the 20-minute period.


Blood ◽  
1973 ◽  
Vol 42 (5) ◽  
pp. 771-781 ◽  
Author(s):  
Paul R. Pedersen ◽  
Paul R. McCurdy ◽  
R. N. Wrightstone ◽  
J. B. Wilson ◽  
L. L. Smith ◽  
...  

Abstract A 17-yr-old black male with hemolysis and pigmenturia but no anemia was found to have hemoglobin Köln (α2β298 val→met [FG5]). Splenectomy was done because of complicating thrombocytopenia. Thrombokinetic studies with 51Cr tagged platelets suggested hypersplenism, and after surgery the platelet count returned to normal. The red cell t ½ 51Cr was more than doubled, but the red cell life span (DF32P) was more modestly improved (30.6 → 47.2 days). The "elution" of 51Cr from the red cells presplenectomy was 5.6%/day, whereas after surgery it was normal (1.9%/day), accounting for the disparity between the survival methods. Study of the isolated cyanferri derivative of hemoglobin Köln by ultracentrifugation at various salt concentrations and various pH’s indicated an increased tendency to dimer formation under conditions where normal hemoglobin is a tetramer. This results from the site and type of amino acid substitution and accounts in part for its instability.


1997 ◽  
Vol 41 (6) ◽  
pp. 916-921 ◽  
Author(s):  
Donald M Mock ◽  
Gary L Lankford ◽  
Leon F Burmeister ◽  
Ronald G Strauss

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