Erythrocyte nucleotides from control and lead-treated rabbits.
Mark S. Swanson, C.R. Angle, Sidney J. Stohs, Karen Rovang
Abstract
Mark S. Swanson, C.R. Angle, Sidney J. Stohs, Karen Rovang
Abstract
Significant abnormal elevations of the erythrocyte pyrimidine nucleotides UTP and CTP were observed in rabbits after 60 days of oral exposure to lead acetate at a dose of 30 mg/kg/day. No significant changes in purine nucleotides were observed. The increased erythrocyte pyrimidine nucleotides were accompanied by a decrease in red cell pyrimidine 5'-nucleotidase (P5N) activity, an increase in zinc erythrocyte protoporphyrin concentration, and elevated whole blood lead levels. Quantitative measurement of the major 5'-nucleotides in rabbit red cells was achieved by high performance liquid chromatography. The accumulation of UTP and CTP as the results of chronic lead exposure may be explained on the basis of inhibited P5N coupled with the presence of an active nucleoside diphosphokinase.
OpenAlex reports 8 citations for this work. Citation counts describe recorded attention and do not establish research quality.
A contribution statement is not available in the OpenAlex record.
Method details are not available in the OpenAlex metadata.
Findings are not separately available in the OpenAlex metadata.
Limitations are not available in the OpenAlex metadata.
Application details are not available in the OpenAlex metadata.
Significant abnormal elevations of the erythrocyte pyrimidine nucleotides UTP and CTP were observed in rabbits after 60 days of oral exposure to lead acetate at a dose of 30 mg/kg/day. No significant changes in purine nucleotides were observed. The increased erythrocyte pyrimidine nucleotides were accompanied by a decrease in red cell pyrimidine 5'-nucleotidase (P5N) activity, an increase in zinc erythrocyte protoporphyrin concentration, and elevated whole blood lead levels. Quantitative measurement of the major 5'-nucleotides in rabbit red cells was achieved by high performance liquid chromatography. The accumulation of UTP and CTP as the results of chronic lead exposure may be explained on the basis of inhibited P5N coupled with the presence of an active nucleoside diphosphokinase.
Key concepts: Nucleotide, Purine, Pyrimidine, Nucleoside, Chemistry, Lead acetate, Biochemistry, Red blood cell