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Artikel: Cortistatin regulates glucose-induced electrical activity and insulin secretion in mouse pancreatic beta-cells

Soriano, Sergi / Alex Rafacho / Ángel Nadal / Antonia Ruiz-Pino / Beatriz Merino / Eduard Montanya / Esperanza Irles / Eva Bru-Tarí / Iván Quesada / Jean F. Vettorazzi / Laura Marroquí / Manuel Castellano-Muñoz / Melisa Bello-Pérez / Paloma Alonso-Magdalena / Pau Iborra / Raúl M. Luque / Sabrina Villar-Pazos

Molecular and cellular endocrinology. 2019 Jan. 05, v. 479

2019  

Abstract: Although there is growing evidence that cortistatin regulates several functions in different tissues, its role in the endocrine pancreas is not totally known. Here, we aim to study the effect of cortistatin on pancreatic beta-cells and glucose-stimulated ...

Abstract Although there is growing evidence that cortistatin regulates several functions in different tissues, its role in the endocrine pancreas is not totally known. Here, we aim to study the effect of cortistatin on pancreatic beta-cells and glucose-stimulated insulin secretion (GSIS). Exposure of isolated mouse islets to cortistatin inhibited GSIS. This effect was prevented using a somatostatin receptor antagonist. Additionally, cortistatin hyperpolarized the membrane potential and reduced glucose-induced action potentials in isolated pancreatic beta-cells. Cortistatin did not modify ATP-dependent K+ (KATP) channel activity. In contrast, cortistatin increased the activity of a small conductance channel with characteristics of G protein-coupled inwardly rectifying K+ (GIRK) channels. The cortistatin effects on membrane potential and GSIS were largely reduced in the presence of a GIRK channel antagonist and by down-regulation of GIRK2 with small interfering RNA. Thus, cortistatin acts as an inhibitory signal for glucose-induced electrical activity and insulin secretion in the mouse pancreatic beta-cell.
Schlagwörter action potentials ; antagonists ; gene expression regulation ; insulin secretion ; islets of Langerhans ; mice ; potassium ; small interfering RNA ; somatostatin receptors
Sprache Englisch
Erscheinungsverlauf 2019-0105
Umfang p. 123-132.
Erscheinungsort Elsevier B.V.
Dokumenttyp Artikel
ZDB-ID 187438-x
ISSN 1872-8057 ; 0303-7207
ISSN (online) 1872-8057
ISSN 0303-7207
DOI 10.1016/j.mce.2018.09.009
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Zs.A 1127: Hefte anzeigen Standort:
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