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首页> 外文期刊>CNS & neurological disorders drug targets >Glycyrrhizic Acid Ameliorates Cognitive Impairment in a Rat Model of Vascular Dementia Associated with Oxidative Damage and Inhibition of Voltage-Gated Sodium Channels
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Glycyrrhizic Acid Ameliorates Cognitive Impairment in a Rat Model of Vascular Dementia Associated with Oxidative Damage and Inhibition of Voltage-Gated Sodium Channels

机译:甘草酸改善血管性痴呆大鼠模型的认知障碍,该模型与氧化性损伤和电压门控钠通道的抑制有关。

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Vascular dementia (VD) is the second most common cause of cognitive impairment in the elderly population. Our study aims to investigate the neuroprotective effects of glycyrrhizic acid (GA), a major active constituent of Glycyrrhiza glabra root, in a VD rat model induced by permanent occlusion of the bilateral common carotid arteries. Spatial cognitive function was examined by the Morris water maze test and synaptic plasticity was explored by assessing long-term potentiation. The results showed that GA (20 mg/kg for 5 days) significantly improved the performance of learning and memory of VD rats in the Morris water maze test and attenuated induction of long-term potentiation. Histopathological studies showed that GA significantly attenuated cell damage in VD rats. Malondialdehyde levels and superoxide dismutase activity were analyzed in the hippocampus and cortex to investigate anti-oxidant status. The results showed that GA decreased the level of lipid peroxidation and increased the activity of superoxide dismutase in VD rats. Lastly, whole-cell patch-clamp analysis was used to examine the effect of GA on voltage-gated sodium channels (VGSCs) in hippocampal CA1 pyramidal neurons. GA (10, 20 and 50 mu M) inhibited the current amplitude of the VGSCs. These results suggest that the neuroprotective effects of GA in VD rats relate to the reduction of oxidative stress and inhibition of VGSCs. Our study provides experimental evidence for the application of GA in the treatment of cognitive deficits induced by Alzheimer's disease, stroke, or traumatic brain injury.
机译:血管性痴呆(VD)是老年人口认知障碍的第二大最常见原因。我们的研究旨在研究甘草根的主要活性成分甘草酸(GA)在双侧颈总动脉永久性闭塞诱发的VD大鼠模型中的神经保护作用。通过莫里斯水迷宫测试检查空间认知功能,并通过评估长期增强作用来探索突触可塑性。结果表明,在莫里斯水迷宫试验中,GA(20 mg / kg,持续5天)显着改善了VD大鼠的学习和记忆能力,并减弱了长期增强诱导。组织病理学研究表明,GA明显减轻了VD大鼠的细胞损伤。分析海马和皮层的丙二醛水平和超氧化物歧化酶活性,以研究其抗氧化状态。结果表明,GA降低了VD大鼠脂质过氧化水平并增加了超氧化物歧化酶的活性。最后,全细胞膜片钳分析用于检查GA对海马CA1锥体神经元电压门控钠通道(VGSC)的影响。 GA(10、20和50μM)抑制了VGSC的电流幅度。这些结果表明,GA在VD大鼠中的神经保护作用与氧化应激的降低和VGSC的抑制有关。我们的研究为GA在治疗阿尔茨海默氏病,中风或颅脑外伤所致认知功能障碍方面的应用提供了实验证据。

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