Diabetes, Vol 37, Issue 6 816-823, Copyright © 1988 by American Diabetes Association
Induction of memory in rat pancreatic islets by tolbutamide. Dependence on ambient glucose level, calcium, and phosphoinositide hydrolysis
WS Zawalich and KC Zawalich
Yale University School of Nursing, New Haven, Connecticut 06536-0740.
The ability of the sulfonylurea tolbutamide to induce insulin output,
increase phosphoinositide (PI) hydrolysis, and modulate the insulin
response to other agonists was assessed. At 200 microM, tolbutamide
increased both insulin release and the efflux of 3H from
[3H]inositol-prelabeled islets only in the presence of 5.5 or 7 mM glucose.
When the glucose level was maintained at 2.75 mM, tolbutamide (200 microM)
had no positive impact on either parameter. The calcium-influx inhibitor
nitrendipine (200 nM) blocked the effects of 200 microM tolbutamide (with 7
mM glucose) on 3H efflux and insulin output. Prior exposure of islets to
tolbutamide (200 microM) in the presence of 7 mM glucose amplified their
subsequent insulin response to 10 mM glucose and 5 mM glyceraldehyde. The
effect of 200 microM tolbutamide (with 7 mM glucose) was blocked by
nitrendipine. Furthermore, the effect of 200 microM tolbutamide was not
observed with 2.75 mM glucose; however, if the level of tolbutamide was
increased to 1 mM, both PI hydrolysis and potentiated release to subsequent
stimulation with 10 mM glucose were observed. Tolbutamide (200 microM with
7 mM glucose) stimulation for 20 min resulted in an increase in 3H efflux
from [3H]inositol-prelabeled islets. Despite the rapid fall in insulin
secretion, elevated rates of 3H efflux persisted long after the removal of
the sulfonylurea from the medium. The duration of the 3H-efflux response
paralleled the duration of potentiation.(ABSTRACT TRUNCATED AT 250 WORDS)