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Journal of Lipid Research, Vol 22, 1142-1147, Copyright © 1981 by Lipid Research, Inc.
I Bjorkhem, P Arner, A Thore and J Ostman
A sensitive and accurate assay of lipolysis has been developed, measuring
the rate of glycerol release from fat cells with a bioluminescent assay.
The rate of glycerol-dependent ATP-consumption in a system consisting of
glycerokinase, ATP, luciferin, and luciferase was determined kinetically as
a decrease of the ATP-induced luminescence and used for calculation of the
concentration of glycerol. Under the conditions employed, it was possible
to measure the concentration of glycerol down to a level of about 0.5
micron mol/l. Under the same conditions, the detection limit of the usual
fluorometric method was about 15 micron mol/l. The coefficient of variation
obtained with the bioluminescent assay was 11% at a level of 1.0 micron mol
of glycerol, 2-6% at a level of about 5 micron mol/l, and 1-3% at a level
of about 20 micron mol/l. Satisfactory results were obtained in different
recovery experiments. Using human fat cells, it was possible to determine
the rate of glycerol release with a cell concentration in the medium of
only 5,000-10,000 cells/ml. It is concluded that the bioluminescent assay
of glycerol release should be preferred when there is a demand for
sensitivity, e.g., when the rate of lipolysis is low and when only a small
amount of biopsy material is available.
ARTICLES
Sensitive kinetic bioluminescent assay of glycerol release from human fat cells
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