Abstract
Prostaglandin E(1) (PGE(1)) at a concentration of 1 ng/ml antagonized theophylline, and norepinephrine induced release of glycerol and free fatty acids (FFA) in human fat cell preparations. Insulin at higher doses also inhibited theophylline-stimulated lipolysis. The N(6)-2-0'dibutyryl derivative of cyclic adenosine monophosphate (DCAMP) stimulated lipolysis. Prostaglandin E(1) did not significantly inhibit the lipid mobilizing effects of DCAMP. Changes in glycogen phosphorylase activity after treatment with theophylline, norepinephrine, DCAMP, and PGE(1) paralleled those of lipolysis. These results suggest that in man as in experimental animals lipolysis and phosphorylase activity are regulated through processes involving cyclic AMP and that PGE(1) appears to exert its antilipolytic effect in human fat cells, as in rat fat cells, by interfering at the level of adenyl cyclase with the accumulation of cyclic AMP.
MeSH Terms
Adenylyl Cyclases/metabolism
Adipose Tissue/cytology,metabolism
Animals
Cyclic AMP
Fatty Acids, Nonesterified/metabolism
Glucosyltransferases/metabolism
Glycerol/metabolism
Humans
Insulin/pharmacology
Lipid Metabolism
Norepinephrine
Prostaglandins/pharmacology,physiology
Rats
Theophylline/antagonists & inhibitors
Chemicals
Fatty Acids, Nonesterified
Insulin
Prostaglandins
Theophylline
Cyclic AMP
Glucosyltransferases
Adenylyl Cyclases
Glycerol
Norepinephrine
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Moskowitz J
Fain J N
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