J Korean Diabetes Assoc.
2000 Oct;24(5):515-523.
The Changes in Insulin Secretion and GTPase Activity after the Exposure to High Glucose in Rat Pancreatic Islets
- Affiliations
-
- 1Department of Internal Medicine, Ewha Womans University College of Medicine, Seoul, Korea.
Abstract
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BACKGROUND: Type 2 diabetes mellitus is characterized by defective glucose-
induced and glucose-potentiated insulin secretion. Chronic elevation of glucose
levels are considered to be a cause of impaired insulin secretion. It has been
suggested that such defects in insulin secretion can be related to the alteration
in stimulus-secretion coupling. Recent studies have provided evidences for the
existence of guanine nucleotide-binding protein (G protein), and the regulatory
role of G protein and GTPase activity in stimulus-secretion coupling in pancreatic
islets.
This study was performed to determine whether the exposure to high glucose
concentration alters GTPase activity with decreased insulin secretion in pancreatic
islets isolated from normal rats.
METHODS
Pancreatic islets isolated from normal Sprague-Dawley rats were
incubated in high (20 mM) and low (5 mM) glucose concentration for 48 hours.
After incubation, glucose (20 mM) induced insulin secretion was measured. Then
subcellular fractions of islets by homogenization and differential centrifugation
were obtained and glucose induced inhibition of GTPase activities in each
fraction was measured.
RESULTS
1) After 48 hour exposure to 5 mM and 20 mM glucose, insulin secretion in
response to 20 mM glucose were 134.4+/-16.8 fmol/10 islets/hr and 90.0+/-10.2
fmol/10 islets/hr, respectively. After the exposure to high glucose, glucose-induced
insulin secretion significantly decreased (p<0.05).
2) In each subcellular fraction, there was no significant difference between the
islets exposed to 5 mM and 20 mM glucose in the degree of inhibition of GTPase
activities by high glucose.
CONCLUSION
The exposure to high glucose for 48 hours decreased insulin secretion
without any significant differences in the degree of inhibition of GTPase activities.
This results suggest that impaired insulin secretion by high glucose is not associated
with the change in GTPase activity.