Endocrinologia Japonica
Online ISSN : 2185-6370
Print ISSN : 0013-7219
ISSN-L : 0013-7219
Effects of Electric Stress on Glucose Metabolism, Glucose-Stimulated Cyclic Adenosine 3', 5'-Monophosphate Accumulation and 45Ca++ Efflux in Isolated Pancreatic Islets from Rats Fed with a High Fat Diet
KEIKO YAMAGUCHIHIDEKI GOKOAKIRA MATSUOKA
著者情報
ジャーナル フリー

1979 年 26 巻 5 号 p. 549-557

詳細
抄録

The effects of the electric stress on glucose oxidation, cyclic adenosine 3', 5'-monophosphate (AMP) accumulation and 45Ca++ efflux in response to glucose were studied in pancreatic islets isolated from rats fed on a control (C) or a high fat diet (F) for 12 weeks.
The half of rats on each diet were subjected to electrical shocks in the random time schedule for1hr per day for the last 3 weeks of the feeding period (group C-S and F-S). The remaining rats were not given any shocks (group C-NS and F-NS). The rats in F-S group had the high levels of plasma epinephrine, dopamine and blood glucose. The basal content of cyclic AMP after 20min of incubation with 2.8mm glucose was decreased in islets from F-S group without affecting insulin release. After 20min of incubation with 25mm glucose, the cyclic AMP content in islets from F-S group, which was identical with that in F-NS group, was only 50% of that in C-S group. Insulin release in response to high glucose was significantly inhibited in islets from F-S group. In spite of a remarkable increase of cyclic AMP content in islets from C-S group, insulin release did not differ from that in C-NS group. Glucose (16.7mm)-stimulated 45Ca++efflux from the perfused islets was greatly inhibited by the high fat diet rather than by stress. The rate of glucose oxidation with 16.7mm glucose was decreased in islets from F-S group.
It is suggested that the decreased insulin release in response to glucose provoked by the combined effects of the feeding of a high fat diet and electric stress may be mediated by changes of the adenylate cyclase-cyclic AMP system on the plasma membrane of the B-cell or be related to changes in glucose metabolism in islets.

著者関連情報
© The Japan Endocrine Society
前の記事 次の記事
feedback
Top