Literature DB >> 24003935

Small-molecule inhibition of inflammatory β-cell death.

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.
© 2013 John Wiley & Sons Ltd.

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


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