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Novel Zn(2+) Modulated GPR39 Receptor Agonists Do Not Drive Acute Insulin Secretion in Rodents

Type 2 diabetes (T2D) occurs when there is insufficient insulin release to control blood glucose, due to insulin resistance and impaired β-cell function. The GPR39 receptor is expressed in metabolic tissues including pancreatic β-cells and has been proposed as a T2D target. Specifically, GPR39 agoni...

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Detalles Bibliográficos
Autores principales: Fjellström, Ola, Larsson, Niklas, Yasuda, Shin-ichiro, Tsuchida, Takuma, Oguma, Takahiro, Marley, Anna, Wennberg-Huldt, Charlotte, Hovdal, Daniel, Fukuda, Hajime, Yoneyama, Yukimi, Sasaki, Kazuyo, Johansson, Anders, Lundqvist, Sara, Brengdahl, Johan, Isaacs, Richard J., Brown, Daniel, Geschwindner, Stefan, Benthem, Lambertus, Priest, Claire, Turnbull, Andrew
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4697807/
https://www.ncbi.nlm.nih.gov/pubmed/26720709
http://dx.doi.org/10.1371/journal.pone.0145849
Descripción
Sumario:Type 2 diabetes (T2D) occurs when there is insufficient insulin release to control blood glucose, due to insulin resistance and impaired β-cell function. The GPR39 receptor is expressed in metabolic tissues including pancreatic β-cells and has been proposed as a T2D target. Specifically, GPR39 agonists might improve β-cell function leading to more adequate and sustained insulin release and glucose control. The present study aimed to test the hypothesis that GPR39 agonism would improve glucose stimulated insulin secretion in vivo. A high throughput screen, followed by a medicinal chemistry program, identified three novel potent Zn(2+) modulated GPR39 agonists. These agonists were evaluated in acute rodent glucose tolerance tests. The results showed a lack of glucose lowering and insulinotropic effects not only in lean mice, but also in diet-induced obese (DIO) mice and Zucker fatty rats. It is concluded that Zn(2+) modulated GPR39 agonists do not acutely stimulate insulin release in rodents.