Ping Li1, Yongfang Zhang2, Hongtao Liu3. 1. Department of Anesthesiology, Shengjing Hospital of China Medical University, Shenyang, 110004, Liaoning, PR China; Department of Anesthesiology, The First Affiliated Hospital of Jingzhou Medical University, Jinzhou, 121001, PR China. 2. Department of Anesthesiology, Shengjing Hospital of China Medical University, Shenyang, 110004, Liaoning, PR China. 3. Department of Anesthesiology, Shengjing Hospital of China Medical University, Shenyang, 110004, Liaoning, PR China. Electronic address: 18040099898@qq.com.
Abstract
AIMS: To assess the role of glycogen synthase kinase-3β (GSK3β) and β-catenin in the protection of ischemic injury by dexmedetomidine (Dex). MAIN METHODS: Adult male Sprague-Dawley rats were subjected to (middle cerebral artery occlusion, MCAO) for 2 h followed by reperfusion and Dex was administered 30min before MCAO. The neurological deficit score, cerebral infarct size and neuron survival were evaluated at 24 h after reperfusion. The expression of pAKT, pGSK3β and β-catenin in the ischemic penumbra was assayed by Western blot at 2 h after reperfusion. KEY FINDINGS: We found that the Dex-induced increment of neuron survival in the ischemic penumbra was diminished by the PI3K inhibitor LY294002 and the β-catenin inhibitor XAV939, respectively. The increasing expression of pAKT, pGSK3β and β-catenin induced by Dex was markedly inhibited by LY294002. And the increasing expression of β-catenin in nuclei induced by Dex was markedly inhibited by XAV939. At the same time, the GSK3β inhibitor SB216763 also caused an increment of neuron survival and an increasing expression of pGSK3β and β-catenin in the ischemic penumbra. SIGNIFICANCE: Our data suggested that treatment with Dex reduced cerebral injury in rats exposed to cerebral ischemia-reperfusion (I/R) by the activation of the PI3K/AKT/GSK3β pathways as well the activation of downstream Wnt/β-catenin pathway. And the Wnt/β-catenin pathway may play an important role in the protection against cerebral ischemia/reperfusion injury in rats.
AIMS: To assess the role of glycogen synthase kinase-3β (GSK3β) and β-catenin in the protection of ischemic injury by dexmedetomidine (Dex). MAIN METHODS: Adult male Sprague-Dawley rats were subjected to (middle cerebral artery occlusion, MCAO) for 2 h followed by reperfusion and Dex was administered 30min before MCAO. The neurological deficit score, cerebral infarct size and neuron survival were evaluated at 24 h after reperfusion. The expression of pAKT, pGSK3β and β-catenin in the ischemic penumbra was assayed by Western blot at 2 h after reperfusion. KEY FINDINGS: We found that the Dex-induced increment of neuron survival in the ischemic penumbra was diminished by the PI3K inhibitor LY294002 and the β-catenin inhibitor XAV939, respectively. The increasing expression of pAKT, pGSK3β and β-catenin induced by Dex was markedly inhibited by LY294002. And the increasing expression of β-catenin in nuclei induced by Dex was markedly inhibited by XAV939. At the same time, the GSK3β inhibitor SB216763 also caused an increment of neuron survival and an increasing expression of pGSK3β and β-catenin in the ischemic penumbra. SIGNIFICANCE: Our data suggested that treatment with Dex reduced cerebral injury in rats exposed to cerebral ischemia-reperfusion (I/R) by the activation of the PI3K/AKT/GSK3β pathways as well the activation of downstream Wnt/β-catenin pathway. And the Wnt/β-catenin pathway may play an important role in the protection against cerebral ischemia/reperfusion injury in rats.
Authors: Yanqun Cao; Jia Liu; Quzhe Lu; Kai Huang; Baolin Yang; James Reilly; Na Jiang; Xinhua Shu; Lei Shang Journal: Int J Mol Med Date: 2022-05-20 Impact factor: 5.314
Authors: Li Gan; Xiaonan Wan; Delin Ma; Fu-Chen Yang; Jingpeng Zhu; Robert S Rogers; Joshua L Wheatley; Lauren G Koch; Steven L Britton; John P Thyfault; Paige C Geiger; John A Stanford Journal: J Alzheimers Dis Rep Date: 2021-06-08