Expression of GLP-1 receptors in insulin-containing interneurons of rat cerebral cortex

Aims/hypothesis Glucagon-like peptide 1 (GLP-1) receptors are expressed by pancreatic beta cells and GLP-1 receptor signalling promotes insulin secretion. GLP-1 receptor agonists have neural effects and are therapeutically promising for mild cognitive impairment and Alzheimer’s disease. Our previous...

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Veröffentlicht in:Diabetologia 2019-04, Vol.62 (4), p.717-725
Hauptverfasser: Csajbók, Éva A., Kocsis, Ágnes K., Faragó, Nóra, Furdan, Szabina, Kovács, Balázs, Lovas, Sándor, Molnár, Gábor, Likó, István, Zvara, Ágnes, Puskás, László G., Patócs, Attila, Tamás, Gábor
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Sprache:eng
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Zusammenfassung:Aims/hypothesis Glucagon-like peptide 1 (GLP-1) receptors are expressed by pancreatic beta cells and GLP-1 receptor signalling promotes insulin secretion. GLP-1 receptor agonists have neural effects and are therapeutically promising for mild cognitive impairment and Alzheimer’s disease. Our previous results showed that insulin is released by neurogliaform neurons in the cerebral cortex, but the expression of GLP-1 receptors on insulin-producing neocortical neurons has not been tested. In this study, we aimed to determine whether GLP-1 receptors are present in insulin-containing neurons. Methods We harvested the cytoplasm of electrophysiologically and anatomically identified neurogliaform interneurons during patch-clamp recordings performed in slices of rat neocortex. Using single-cell digital PCR, we determined copy numbers of Glp1r mRNA and other key genes in neurogliaform cells harvested in conditions corresponding to hypoglycaemia (0.5 mmol/l glucose) and hyperglycaemia (10 mmol/l glucose). In addition, we performed whole-cell patch-clamp recordings on neurogliaform cells to test the effects of GLP-1 receptor agonists for functional validation of single-cell digital PCR results. Results Single-cell digital PCR revealed GLP-1 receptor expression in neurogliaform cells and showed that copy numbers of mRNA of the Glp1r gene in hyperglycaemia exceeded those in hypoglycaemia by 9.6 times ( p  
ISSN:0012-186X
1432-0428
DOI:10.1007/s00125-018-4803-z