TY - JOUR
T1 - Low apparent creatine kinase activity and prolonged lag phases in serum of patients with metastatic disease
T2 - elimination by treatment of sera with sulfhydryl agents
AU - Bruns, D. E.
AU - Morgan, W. S.
AU - Davis, J. E.
AU - Ladenson, J. H.
N1 - Copyright:
Copyright 2020 Elsevier B.V., All rights reserved.
PY - 1976
Y1 - 1976
N2 - The authors fing lag phases exceeding 20 min in measuring creatine kinase activity, by using the kinetic creatine phosphate → creatine assay, in sera of some patients with carcinoma metastatic to the liver. Such long lag phases are accompanied by a decreased apparent enzyme activity. These problems are eliminated by adding sulfhydryl agents to the serum before assay, but not by adding more of such agents to the assay reagent. β Mercaptoethanol is superior to Cleland's reagents, glutathione, and cysteine. The long lag phases could not be explained by inadequate activity of the coupling enzymes, interference with the coupling steps, high proportions of cardiac isoenzyme activity, simple oxidation of the enzyme, low concentrations of albumin, or increased concentrations of glutathione reductase, lactate dehydrogenase, or uric acid. It is concluded that the prolonged lag phases reflect inadequate reactivation of the enzyme by sulfhydryl agents under the usual assay conditions. Reactivation before assay can prevent potentially serious negative errors in the assay of creatine kinase.
AB - The authors fing lag phases exceeding 20 min in measuring creatine kinase activity, by using the kinetic creatine phosphate → creatine assay, in sera of some patients with carcinoma metastatic to the liver. Such long lag phases are accompanied by a decreased apparent enzyme activity. These problems are eliminated by adding sulfhydryl agents to the serum before assay, but not by adding more of such agents to the assay reagent. β Mercaptoethanol is superior to Cleland's reagents, glutathione, and cysteine. The long lag phases could not be explained by inadequate activity of the coupling enzymes, interference with the coupling steps, high proportions of cardiac isoenzyme activity, simple oxidation of the enzyme, low concentrations of albumin, or increased concentrations of glutathione reductase, lactate dehydrogenase, or uric acid. It is concluded that the prolonged lag phases reflect inadequate reactivation of the enzyme by sulfhydryl agents under the usual assay conditions. Reactivation before assay can prevent potentially serious negative errors in the assay of creatine kinase.
UR - http://www.scopus.com/inward/record.url?scp=0017089005&partnerID=8YFLogxK
U2 - 10.1093/clinchem/22.11.1889
DO - 10.1093/clinchem/22.11.1889
M3 - Article
C2 - 975550
AN - SCOPUS:0017089005
SN - 0009-9147
VL - 22
SP - 1889
EP - 1895
JO - Clinical chemistry
JF - Clinical chemistry
IS - 11
ER -