GLPwatch

Circulating microRNA-375 as biomarker of pancreatic beta cell death and protection of beta cell mass by cytoprotective compounds.

PLoS One · 2017

Last updated 2026-05-28

In a study on mice, researchers found that a marker called microRNA-375 in the blood increased when pancreatic beta cells were damaged by a drug called streptozotocin (STZ). However, when the mice were treated with either PPAG or exendin-4, two compounds known to protect beta cells, the levels of microRNA-375 returned to normal, and the loss of beta cells was reduced.

AI summary of the abstract below.

JournalPLoS One, 2017
Citations26
Relative citation ratio1.05
NIH percentile52
Molecules
Conditions studied Type 2 Diabetes

Abstract

OBJECTIVE: Previous studies demonstrated that circulating microRNA-375 (miR-375) is a suitable plasma biomarker for real-time detection of beta cell death. The present study evaluated the use of this biomarker to assess the beta cytoprotective effect of phenylpropenoic acid glucoside (PPAG), which was previously demonstrated to protect beta cells against various types of injury, and of exendin-4, which is an established antidiabetic drug. METHODS: PPAG or exendin-4 were administered in mice treated with streptozotocin (STZ) to acutely induce beta cell death. Beta cell mass and apoptotic death were measured in pancreatic tissue sections. Circulating miR-375 was measured in blood plasma by RT-qPCR. The release of miR-375 was also measured in vitro by MIN-6 beta cells. RESULTS: Administration of STZ resulted in measurable circulating levels of miR-375, a decrease in beta cell mass and increase in frequency of apoptotic beta cells. In vitro, there was a good correlation between miR-375 release and the extent of beta cell death. Treatment of mice with PPAG or exendin-4 significantly attenuated STZ-induced loss of beta cell mass and beta cell apoptosis, and normalized the blood level of miR-375. CONCLUSIONS: These findings show the potential use of serological miR-375 measurements to evaluate the beta cytoprotective effect of (potential) antidiabetic drugs in vivo.

Verbatim abstract via PubMed 29040320 ↗