[Effect of liraglutide on interleukin-1β expression in the pancreatic islets of OLETF rats].
Nan Fang Yi Ke Da Xue Xue Bao · 2012
Last updated 2026-05-28In a study on rats, liraglutide at doses of 50, 100, or 200 µg/kg twice daily for 12 weeks reduced levels of the inflammatory marker IL-1β and the cell-death marker caspase-3 in pancreatic islets. The drug also improved blood sugar control, insulin function, and early insulin release compared to rats given only saline.
AI summary of the abstract below.
| Journal | Nan Fang Yi Ke Da Xue Xue Bao, 2012 |
|---|---|
| Citations | 0 |
| Relative citation ratio | 0.00 |
| NIH percentile | 0 |
| Molecules | liraglutide |
| Conditions studied | Type 2 Diabetes |
Abstract
OBJECTIVE: To investigate the effect of liraglutide on the inflammatory cytokine interleukin-1β (IL-1β) and apoptotic factor caspase-3 expression in the pancreatic islets of OLETF rats with impaired glucose tolerance.
METHODS: Twelve-week-old OLETF rats were randomized into 4 groups and received intraperitoneal injections of saline or liraglutide at 50, 100, or 200 µg/kg twice daily for 12 weeks. Eight LETO rats served as the normal control group and received saline injection. After the treatments, the rats were examined for fasting and 30 min plasma insulin during OGTT test, and the expression levels of IL-1β and caspase-3 mRNA and protein in the pancreatic islets were detected by real-time PCR and Western blotting, respectively.
RESULTS: Compared with the saline group, liraglutide significantly decreased the expressions of IL-1β and caspase-3 mRNA and protein, and significantly improved the blood glucose, islet β function and early-phase insulin secretion index in OLETF rats.
CONCLUSIONS: Liraglutide can improve islet function and glucose metabolism partially by inhibiting islet IL-1β expression to delay or prevent the development of diabetes in OLETF rats.
Verbatim abstract via PubMed 22699075 ↗
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