Abstract
The dose response effect of a new adenosine analogue, GR79236 (N-[1S trans-2-hydroxycyclopentyl] adenosine) upon insulin sensitivity was examined in human adipocytes. The influence of adenosine upon insulin sensitivity for suppression of lipolysis and stimulation of glucose transport was examined. Removal of adenosine by use of adenosine deaminase stimulated lipolysis to the same extent as did 10(-9) M noradrenaline. GR79236 brought about dose dependent inhibition of lipolysis with half-maximal effect at 11.3 +/- 7.8 x 10(-9) M. When lipolysis was stimulated by noradrenaline alone the subsequent inhibition of lipolysis brought about by GR79236 was significantly greater than that of insulin. To examine adenosine effects on the insulin signalling pathway separately from those on lipolysis, the insulin sensitivity of glucose transport was examined. Removal of adenosine brought about a small but significant increase in the concentration of insulin required for half-maximal stimulation of glucose transport. Adenosine agonists offer promise as new agents for the modulation of metabolism in diabetes and other states of insulin resistance.
MeSH Terms
3-O-Methylglucose
Adenosine/analogs & derivatives,metabolism,pharmacology
Adenosine Deaminase/metabolism
Adipocytes/metabolism
Dose-Response Relationship, Drug
Glucose/pharmacology
Glycerol/metabolism
Humans
In Vitro Techniques
Insulin/metabolism
Lipolysis
Methylglucosides/metabolism
Norepinephrine/pharmacology
Purinergic P1 Receptor Agonists
Signal Transduction
Chemicals
Insulin
Methylglucosides
Purinergic P1 Receptor Agonists
3-O-Methylglucose
Adenosine Deaminase
Glucose
Adenosine
Glycerol
N-((1S,trans)-2-hydroxycyclopentyl)adenosine
Norepinephrine
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Heseltine L
Human Metabolism Research Centre, Medical School, University of Newcastle upon Tyne, UK.
Webster J M
Taylor R
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