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The Synthesis of Pyridine Nucleotides in Fresh and Stored Human Erythrocytes *
Author(s) -
Jaffé Ernst R.,
Neumann Gertrude
Publication year - 1965
Publication title -
transfusion
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.045
H-Index - 132
eISSN - 1537-2995
pISSN - 0041-1132
DOI - 10.1111/j.1537-2995.1965.tb02917.x
Subject(s) - inosine , nicotinamide , nucleotide , incubation , pyridine , chemistry , biochemistry , purine , nad+ kinase , purine metabolism , in vitro , metabolism , incubation period , medicinal chemistry , adenosine , enzyme , gene
The concentrations of total oxidized pyridine nucleotides and of DPN did not decrease significantly in normal human erythrocytes during storage at 4C in acid‐citrate‐dextrose solution for periods up to 47 days. The capacity of washed erythrocytes which had survived storage to incorporate radioactive nicotinic acid and nico‐tinamide into DPN and TPN during a four‐hour period of incubation at 37 C declined progressively with aging in vitro . The net synthesis of total oxidized pyridine nucleotides and of DPN from nicotinic acid and of total oxidized pyridine nucleotides from nicotinamide also was decreased in these erythrocytes. Addition of inosine to the incubation medium inhibited both incorporation and synthesis by erythrocytes stored for less than three to four weeks. The purine nudeoside enhanced incorporation and synthesis by cells stored for more than about 30 days. It was suggested that the availability of substrates, such as ATP or phosphoribosylpyrophosphate, influenced the extent of pyridine nudeotide synthesis.