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Canine cyclic hematopoiesis is associated with abnormal purine and pyrimidine metabolism
Insights
Canine cyclic hematopoiesis in grey collies involves abnormal purine/pyrimidine metabolism, leading to cyclical blood cell count fluctuations. Lithium treatment normalized metabolite levels, suggesting a metabolic cause for defective stem cell proliferation.
Area of Science:
- Veterinary Medicine
- Hematology
- Biochemistry
Background:
- Canine cyclic hematopoiesis is an autosomal recessive disorder in grey collies.
- It causes regular 11-13 day cycles in neutrophil, reticulocyte, and platelet counts.
- This is linked to defective regulation of marrow stem cell proliferation.
Purpose of the Study:
- To investigate potential abnormalities in purine or pyrimidine metabolism in grey collies with cyclic hematopoiesis.
- To determine if lithium treatment affects these metabolic pathways.
Main Methods:
- High-pressure liquid chromatography (HPLC) was used to measure erythrocyte nucleotide and plasma nucleoside/base levels.
- Measurements were taken in normal and grey collie dogs before and during lithium treatment.
- Comparisons were made with normal dogs made neutropenic using cyclophosphamide.
Main Results:
- Grey collies showed elevated erythrocyte ATP, GTP, and UTP during neutropenic periods.
- Plasma thymine levels were also markedly increased in neutropenic grey collies.
- Lithium treatment normalized these elevated metabolite levels in grey collies.
Conclusions:
- Abnormal concentrations of purine and pyrimidine metabolites were found in grey collies with cyclic hematopoiesis.
- These findings suggest a metabolic derangement in purine or pyrimidine metabolism may underlie the defective stem cell proliferation in this disease.
Abstract:
Canine cyclic hematopoiesis is an autosomal recessive disease characterized by regular 11-13-d cycles of the neutrophil, reticulocyte, and platelet counts caused by a defect in regulation of marrow stem cell proliferation. Treatment with lithium abrogates cycling of the cell counts in these grey collie dogs. Aware of the defective lymphopoiesis associated with adenosine deaminase and purine nucleoside phosphorylase deficiencies, we hypothesized that abnormal purine or pyrimidine metabolism might be present in these dogs. Using high pressure liquid chromatography, we measured erythrocyte purine and pyrimidine nucleotide levels and plasma purine and pyrimidine nucleosides and bases in normal and grey collie dogs before and during lithium treatment. During neutropenic periods in the grey collies, erythrocyte ATP, GTP, and UTP levels were significantly elevated. Normal dogs made neutropenic with cyclophosphamide did not show such elevations. Lithium treatment normalized the levels of erythrocyte ATP, GTP, and UTP in the grey collies and eliminated the differences between normal and grey collie nucleotide levels. Plasma thymine levels were markedly increased during neutropenia in the grey collie but were not increased in cyclophosphamide-treated normal dogs. The finding of abnormal concentrations of purine and pyrimidine metabolites in these dogs suggest that a metabolic derangement in purine or pyrimidine metabolism may be the cause of the defective stem cell proliferation in this disease.
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