Neuroprotective effects of liraglutide for stroke model of rats.
Int J Mol Sci · 2013
Last updated 2026-05-28In a rat stroke model, liraglutide—a GLP-1 drug—improved behavioral scores and reduced brain damage compared to a control group. The treated rats also showed lower oxidative stress and increased levels of a protein called VEGF in the brain cortex, suggesting possible protective effects.
AI summary of the abstract below.
| Journal | Int J Mol Sci, 2013 |
|---|---|
| Citations | 102 |
| Relative citation ratio | 3.32 |
| NIH percentile | 86 |
| Molecules | liraglutide |
| Conditions studied | Alzheimers, Parkinsons |
Abstract
The number of diabetes mellitus (DM) patients is increasing, and stroke is deeply associated with DM. Recently, neuroprotective effects of glucagon-like peptide-1 (GLP-1) are reported. In this study, we explored whether liraglutide, a GLP-1 analogue exerts therapeutic effects on a rat stroke model. Wistar rats received occlusion of the middle cerebral artery for 90 min. At one hour after reperfusion, liraglutide or saline was administered intraperitoneally. Modified Bederson's test was performed at 1 and 24 h and, subsequently, rats were euthanized for histological investigation. Peripheral blood was obtained for measurement of blood glucose level and evaluation of oxidative stress. Brain tissues were collected to evaluate the level of vascular endothelial growth factor (VEGF). The behavioral scores of liraglutide-treated rats were significantly better than those of control rats. Infarct volumes of liraglutide-treated rats at were reduced, compared with those of control rats. The level of derivatives of reactive oxygen metabolite was lower in liraglutide-treated rats. VEGF level of liraglutide-treated rats in the cortex, but not in the striatum significantly increased, compared to that of control rats. In conclusion, this is the first study to demonstrate neuroprotective effects of liraglutide on cerebral ischemia through anti-oxidative effects and VEGF upregulation.
Verbatim abstract via PubMed 24177570 ↗
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