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Gastrin releasing peptide augments glucose mediated 45Ca2+ uptake, electrical activity, and insulin secretion of mouse pancreatic islets

Journal Article · · Endocrinology; (United States)
; ; ; ;  [1]
  1. Department of Pharmacology, Eberhard-Karls Universitaet Tuebingen (West Germany)
Gastrin releasing peptide (GRP) has recently been shown to increase glucose-induced insulin secretion in vivo. Being present in pancreatic tissue, the 27-amino acid peptide could play a role in the control of the glucose-induced insulin secretion of islets of Langerhans. In the presence of a stimulatory glucose concentration, GRP augmented insulin secretion of isolated islets in batch incubations. The peptide did not affect 86Rb+ efflux in the presence of 3 or 5.6 mM glucose but reduced the increase of 86Rb+ efflux evoked by the calcium ionophore A23187. 45Ca2+ uptake and intracellular recorded electrical activity induced by glucose were amplified by GRP. It is suggested that GRP plays a role in the regulation of glucose-induced insulin secretion by increasing the uptake of Ca2+ directly or by inhibition of the Ca(2+)-dependent K+ channel activity and reduced repolarization of the cell.
OSTI ID:
5596098
Journal Information:
Endocrinology; (United States), Journal Name: Endocrinology; (United States) Vol. 128:6; ISSN ENDOA; ISSN 0013-7227
Country of Publication:
United States
Language:
English

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