| Literature DB >> 18345612 |
Hendrik Stukenbrock1, Rainer Mussmann, Marcus Geese, Yoan Ferandin, Olivier Lozach, Thomas Lemcke, Simone Kegel, Alexander Lomow, Ulrike Burk, Cord Dohrmann, Laurent Meijer, Matthias Austen, Conrad Kunick.
Abstract
Recently, the serine/threonine kinase glycogen synthase kinase-3 (GSK-3) emerged as a regulator of pancreatic beta cell growth and survival. On the basis of the previous observation that GSK-3 inhibitors like 1-azakenpaullone promote beta cell protection and replication, paullone derivatives were synthesized including 1-aza-, 2-aza-, and 12-oxapaullone scaffolds. In enzymatic assays distinct 1-azapaullones were found to exhibit selective GSK-3 inhibitory activity. Within the series of 1-azapaullones, three derivatives stimulated INS-1E beta cell replication and protected INS-1E cells against glucolipotoxicity induced cell death. Cazpaullone (9-cyano-1-azapaullone), the most active compound in the protection assays, also stimulated the replication of primary beta cells in isolated rat islets. Furthermore, cazpaullone showed a pronounced transient stimulation of the mRNA expression of the beta cell transcription factor Pax4, an important regulator of beta cell development and growth. These features distinguish cazpaullone as a unique starting point for the development of beta cell regenerative agents which might be useful in the treatment of diabetes.Entities:
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Year: 2008 PMID: 18345612 DOI: 10.1021/jm701582f
Source DB: PubMed Journal: J Med Chem ISSN: 0022-2623 Impact factor: 7.446