Key result
Post-reperfusion liraglutide reduces infarct volume and improves neurobehavioral scores versus saline in rats.
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.
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Sato et al. (2013) studied Cerebral ischemia / stroke (middle cerebral artery occlusion rat model). Liraglutide vs. Saline was evaluated on Behavioral scores (Modified Bederson's test), infarct volume, oxidative stress (reactive oxygen metabolite derivatives), and cortical VEGF levels. Liraglutide administered 1 h post-reperfusion significantly improved 1- and 24-h behavioral scores, reduced infarct volume and oxidative stress, and increased cortical VEGF vs saline in rats.
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