THE LACK OF BIMODALITY IN THE EFFECTS OF ENDOGENOUS AND EXOGENOUS PROSTAGLANDINS ON FAT-CELL LIPOLYSIS IN RATS

Citation
H. Girouard et R. Savard, THE LACK OF BIMODALITY IN THE EFFECTS OF ENDOGENOUS AND EXOGENOUS PROSTAGLANDINS ON FAT-CELL LIPOLYSIS IN RATS, PROSTAGLANDINS & OTHER LIPID MEDIATORS, 56(1), 1998, pp. 43-52
Citations number
31
Categorie Soggetti
Cell Biology",Biology
ISSN journal
10988823
Volume
56
Issue
1
Year of publication
1998
Pages
43 - 52
Database
ISI
SICI code
0090-6980(1998)56:1<43:TLOBIT>2.0.ZU;2-N
Abstract
The aim of this study was to investigate and clarify the role of prost aglandins (PG) on fat cell lipolysis in female rats. Incubations with adenosine deaminase (ADA) were used for the deamination of endogenous adenosine and increased basal (155%) and isoproterenol (10(-9) M) (348 %) stimulation of glycerol release from adipocytes. Indomethacin and a spirin increased the effects of ADA while indomethacin further increas ed isoproterenol (with ADA) stimulation of lipolysis (p less than or e qual to 0.05). Exogenous PGE(2) and PGI(2) inhibited the isoproterenol and ADA stimulation of fat cell lipolysis (p less than or equal to 0. 05). The expected stimulatory effect of high concentrations of PGE, an d of low concentrations of PGI(2) was not observed in the presence of ADA. Dose-response curves revealed that the inhibitory effects of PGs were reached at lower concentrations for PGE(2) than for PGI(2) (p les s than or equal to 0.05). In conclusion, this study showed that endoge nous and exogenous PGs of adipose tissue only express an antilipolytic action on fat cell lipolysis. This effect appears to be highly signif icant when the beta-adrenergic pathway is stimulated. Our results also stress the need to control the antilipolytic effects of adenosine to study the regulation of fat cell lipolysis by PGs.