IN-VIVO AND IN-VITRO INCREASED PANCREATIC BETA-CELL SENSITIVITY TO GLUCOSE IN NORMAL RATS SUBMITTED TO A 48-H HYPERGLYCEMIC PERIOD

Citation
C. Thibault et al., IN-VIVO AND IN-VITRO INCREASED PANCREATIC BETA-CELL SENSITIVITY TO GLUCOSE IN NORMAL RATS SUBMITTED TO A 48-H HYPERGLYCEMIC PERIOD, Diabetologia, 36(7), 1993, pp. 589-595
Citations number
26
Categorie Soggetti
Endocrynology & Metabolism","Medicine, General & Internal
Journal title
ISSN journal
0012186X
Volume
36
Issue
7
Year of publication
1993
Pages
589 - 595
Database
ISI
SICI code
0012-186X(1993)36:7<589:IAIIPB>2.0.ZU;2-8
Abstract
We investigated the importance of the level and the duration of glucos e stimulation on the in vivo and in vitro insulin response to glucose in normal rats previously submitted to hyperglycaemia. Rats were made hyperglycaemic by a 48-h glucose infusion. Glucose-induced insulin sec retion was investigated in vivo by a 20-min hyperglycaemic clamp and i n vitro by the isolated perfused pancreas technique, 3 h after the end of the in vivo glucose infusion. In glucose-infused rats, as compared to controls, in vivo incremental plasma insulin values above baseline integrated over the 20-min hyperglycaemic clamp (DELTAI) were five ti mes higher during 8 mmol/l glucose clamp, only two times higher in 11 mmol/l glucose clamp and no different in 16.5 mmol/l. Compared to the controls, in vitro incremental plasma insulin concentration above base line integrated over a 20-min period (DELTAI) in glucose-infused rats was 16 times higher in response to 2.8 mmol/l glucose, two times highe r in response to 5.5 mmol/l, similar in response to 8.3 mmol/l and sig nificantly lower in response to 16.5 mmol/l. In conclusion, our data s uggest that a 48-h hyperglycaemic period results in an increased respo nse of the pancreatic beta cell to low glucose. The response is immedi ately maximal and can not be increased with higher glucose concentrati ons. This situation could explain the apparent minimal effect of high concentrations on in vitro insulin secretion in previously hyperglycae mic rats and may provide insights into the sequence of events leading to the impairment of beta-cell function in Type 2 (non-insulin-depende nt) diabetes mellitus.