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<dc:creator>García Calvo, José</dc:creator>
<dc:creator>Torroba Pérez, Tomás</dc:creator>
<dc:creator>Brañas‐Fresnillo, Virginia</dc:creator>
<dc:creator>Perdomo Hernández, Germán M.</dc:creator>
<dc:creator>Cózar Castellano, Irene</dc:creator>
<dc:creator>Li, Yu‐Hao</dc:creator>
<dc:creator>Legrand, Yves‐Marie</dc:creator>
<dc:creator>Barboiu, Mihail</dc:creator>
<dc:date>2019-05</dc:date>
<dc:description>The cyclic depsipeptide cereulide toxin it is a very well-known potassium electrogenic ionophore particularly sensitive to pancreatic beta cells. The mechanistic details of its specific activity are unknown. Here, we describe a series of synthetic substituted cereulide potassium ionophores that cause impressive selective activation of glucose-induced insulin secretion in a constitutive manner in rat insulinoma INS1E cells. Our study demonstrates that the different electroneutral K+ transport mechanism exhibited by the anionic mutant depsipeptides when compared with classical electrogenic cereulides can have an important impact of pharmacological value on glucose-stimulated insulin secretion.</dc:description>
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<dc:language>eng</dc:language>
<dc:publisher>Wiley-VCH Verlag</dc:publisher>
<dc:title>Manipulation of Transmembrane Transport by Synthetic K+ Ionophore Depsipeptides and Its Implications in Glucose‐Stimulated Insulin Secretion in β‐Cells</dc:title>
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