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Exendin-4 Promotes Beta Cell Proliferation via PI3k/Akt Signalling Pathway.

Cell Physiol Biochem · 2015

Last updated 2026-05-28

In lab and animal studies, the drug Exendin-4 increased the growth of insulin-producing beta cells by 1.5 to 2 times compared to controls. The effect was blocked when a specific signaling pathway called PI3K/Akt was turned off, but not when other pathways were blocked.

AI summary of the abstract below.

JournalCell Physiol Biochem, 2015
Citations28
Relative citation ratio1.01
NIH percentile51
Molecules
Conditions studied Type 2 Diabetes

Abstract

BACKGROUND/AIMS: Prevention of diabetes requires maintenance of a functional beta-cell mass, the postnatal growth of which depends on beta cell proliferation. Past studies have shown evidence of an effect of an incretin analogue, Exendin-4, in promoting beta cell proliferation, whereas the underlying molecular mechanisms are not completely understood. METHODS: Here we studied the effects of Exendin-4 on beta cell proliferation in vitro and in vivo through analysing BrdU-incorporated beta cells. We also analysed the effects of Exendin-4 on beta cell mass in vivo, and on beta cell number in vitro. Then, we applied specific inhibitors of different signalling pathways and analysed their effects on Exendin-4-induced beta cell proliferation. RESULTS: Exendin-4 increased beta cell proliferation in vitro and in vivo, resulting in significant increases in beta cell mass and beta cell number, respectively. Inhibition of PI3K/Akt signalling, but not inhibition of either ERK/MAPK pathway, or JNK pathway, significantly abolished the effects of Exendin-4 in promoting beta cell proliferation. CONCLUSION: Exendin-4 promotes beta cell proliferation via PI3k/Akt signaling pathway.

Verbatim abstract via PubMed 25895469 ↗