Small-molecule inhibition of inflammatory β-cell death.

Diabetes Obes Metab
Authors
Keywords
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.

Year of Publication
2013
Journal
Diabetes Obes Metab
Volume
15 Suppl 3
Pages
176-84
Date Published
2013 Sep
ISSN
1463-1326
DOI
10.1111/dom.12158
PubMed ID
24003935
PubMed Central ID
PMC3777666
Links
Grant list
DP2 DK083048 / DK / NIDDK NIH HHS / United States