| Literature DB >> 24003935 |
M Lundh1, S S Scully, T Mandrup-Poulsen, B K Wagner.
Abstract
With the worldwide increase in diabetes prevalence there is a pressing unmet need for novel antidiabetic therapies. Insufficient insulin production due to impaired β-cell function and apoptotic reduction of β-cell mass is a common denominator in the pathogenesis of diabetes. Current treatments are directed at improving insulin sensitivity, and stimulating insulin secretion or replacing the hormone, but do not target progressive apoptotic β-cell loss. Here we review the current development of small-molecule inhibitors designed to rescue β-cells from apoptosis. Several distinct classes of small molecules have been identified that protect β-cells from inflammatory, oxidative and/or metabolically induced apoptosis. Although none of these have yet reached the clinic, β-cell protective small molecules alone or in combination with current therapies provide exciting opportunities for the development of novel treatments for diabetes.Entities:
Keywords: apoptosis; glucolipotoxicity; glucotoxicity; inflammation; lipotoxicity; proinflammatory cytokines; small-molecules; β-cell
Mesh:
Substances:
Year: 2013 PMID: 24003935 PMCID: PMC3777666 DOI: 10.1111/dom.12158
Source DB: PubMed Journal: Diabetes Obes Metab ISSN: 1462-8902 Impact factor: 6.577