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Journal of Lipid Research, Vol 17, 68-73, Copyright © 1976 by Lipid Research, Inc.
C Ip, HM Tepperman and J Tepperman
The present study was undertaken to investigate the potentiation by p-
chlorophenoxyisobutyrate (CPIB) of the antilipolytic effect of insulin in
isolated adipocytes from rats fed a (1) sucrose diet, (2) glycerol- lard
diet, or (3) chow diet. CPIB supplementation in the diet consistently
resulted in decreased serum triglyceride levels in rats from the three
dietary groups. The catecholamine-stimulated glycerol release was
significantly depressed to a greater extent by insulin when the fat cells
were obtained from rats given CPIB compared to those without drug
treatment. The enhanced insulin sensitivity was, however, not accompanied
by any changes in insulin binding to adipocytes. These two observations
were found in cell preparations from rats fed any one of the diets,
although differences among dietary groups could be detected. In an in vitro
experiment, epinephrine-stimulated glycerol release was progressively
inhibited by increasing concentrations of CPIB in the incubation medium.
However, the antilipolytic response to an optimal concentration of insulin
(100 muU/ml) was augmented in the presence of CPIB. Thus, it seems that
CPIB can potentiate the action of insulin in inhibiting mobilization of
free fatty acid from the adipose tissue, and the coordinated effect of both
antilipolytic agents is important in lowering serum triglyceride
concentration. The mechanism by which CPIB facilitates the effect of
insulin is discussed.
ARTICLES
Effect of p-chlorophenoxyisobutyrate on the antilipolytic action of insulin and insulin binding in isolated adipocytes
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