基于"肾脑相济"理论探讨归肾丸对亚急性衰老模型小鼠学习记忆的作用机制OA
Deciphering Mechanism of Guishen Wan on Learning and Memory in A Sub-acute Aging Mouse Model via Kidney-brain Axis
目的:评价归肾丸对D-半乳糖衰老模型小鼠学习记忆能力的影响及探讨中医"肾脑相济"理论在老年记忆减退中的应用.方法:采用KM雄性小鼠颈背部皮下注射D-半乳糖(200 mg·kg-1)构建亚急性衰老模型小鼠,随机分成空白组,模型组,归肾丸高、中、低剂量组(18、9、4.5 g·kg-1·d-1),阳性药组(多奈哌齐2 mg·kg-1·d-1),选用临床常用治疗阿尔茨海默病的药物多奈哌齐为阳性药组,连续给药4周.通过水迷宫评价模型小鼠的学习记忆能力;采用马松(Masson)染色观察小鼠肾脏纤维化程度;采用苏木素-伊红(HE)染色观察小鼠海马神经元损伤情况;采用尼氏染色观察小鼠海马尼氏体损伤情况;采用免疫荧光观察小鼠海马中克老素蛋白(Klotho)的荧光表达强度;采用蛋白免疫印迹法(Western blot)检测小鼠肾脏Klotho蛋白表达情况,检测小鼠海马炎症通路、炎症因子相关信号通路蛋白表达情况.结果:水迷宫结果显示,与空白组比较,模型组小鼠穿越平台次数与目标象限停留时间显著减少(P<0.01);与模型组比较,归肾丸各剂量组可使模型小鼠潜穿越平台次数与目标象限停留时间显著增加(P<0.01).Masson染色结果显示,与空白组比较,模型组胶原容积分数显著增加(P<0.01);与模型组比较,归肾丸各剂量组使模型组的胶原容积分数显著降低(P<0.01).肾脏Western blot显示,与空白组比较,模型组小鼠肾脏Klotho蛋白显著下降(P<0.01);与模型组比较,归肾丸可显著提升Klotho蛋白(P<0.01).神经元细胞数量显示,与空白组比较,模型组神经元数量显著降低(P<0.01);与模型组比较,归肾丸对神经元细胞的影响呈现递增趋势,显著修复神经元受损细胞(P<0.01).免疫荧光结果显示,与空白组比较,模型组小鼠Klotho的阳性表达显著减少(P<0.01);与模型组比较,归肾丸各剂量组可显著增强Klotho的荧光表达(P<0.01).海马Western blot显示,与空白组比较,模型组白细胞介素(IL)-1β与IL-6蛋白表达显著升高(P<0.01);与模型组比较,归肾丸各剂量组的IL-1β与IL-6蛋白表达显著降低(P<0.01).与空白组比较,模型组磷酸化核转录因子-κB(p-NF-κB)蛋白表达显著升高(P<0.01),Klotho蛋白表达显著降低(P<0.01);与模型组比较,归肾丸各组p-NF-κB蛋白表达明显降低(P<0.05,P<0.01),Klotho蛋白表达显著降低(P<0.01).结论:归肾丸有效改善D-半乳糖诱导的衰老模型小鼠,其作用机制可能与上调Klotho浓度,抑制NF-κB信号通路相关炎症因子有关.
Objective:To evaluate the Effect of Guishen Wan on learning and memory ability in D-galactose-induced aging model mice and to explore the application of the"Kidney-Brain Coordination"theory in traditional Chinese medicine(TCM).Methods:An subacute aging mouse model was established by subcutaneous injection of D-galactose(200 mg·kg-1·d-1)into the neck and back of KM mice.The mice were then administered GuiShen Wan at high,medium,and low doses(18,9,4.5 g·kg-1·d-1)or donepezil(2 mg·kg-1·d-1),a standard clinical therapeutic agent for Alzheimer's disease,served as the positive control in this study,for 4 consecutive weeks.Learning and memory abilities were evaluated using the Morris water maze.The degree of renal fibrosis was observed via Masson staining.Hippocampal neuron injury was assessed by hematoxylin-eosin(HE)staining.Damage to Nissl bodies in the hippocampus was examined using Nissl staining.The fluorescence expression intensity of Klotho in the hippocampus was detected by immunofluorescence.Western blot was used to detect the protein expression of Klotho in the kidneys,as well as proteins related to the hippocampal inflammatory pathway and inflammatory factor-related signaling pathways.Results:Results from the water maze test showed that compared with the blank group,the number of platform crossings and the time spent in the target quadrant were significantly decreased in the model group(P<0.01).Compared with the model group,all dose groups of Guishen Wan significantly increased the number of platform crossings and the time spent in the target quadrant in model mice(P<0.01).Masson staining results showed that compared with the blank group,the collagen volume fraction was significantly increased in the model group(P<0.01).Compared with the model group,all dose groups of Guishen Wan significantly reduced the collagen volume fraction in the model group(P<0.01).Kidney Western blot analysis showed that compared with the blank group,the Klotho protein was significantly decreased in the model group(P<0.01).Compared with the model group,Guishen Wan elevated the klotho protein(P<0.01).Neuronal cell count results showed that compared with the blank group,the number of neurons was significantly reduced in the model group(P<0.01).Compared with the model group,Guishen Wan exhibited a dose-dependent trend in repairing neuronal damage and increasing the number of neuronal cells(P<0.01).Immunofluorescence intensity results showed that compared with the blank group,the positive expression of Klotho was significantly decreased in the model group(P<0.01).Compared with the model group,all dose groups of Guishen Wan enhanced Klotho fluorescence expression(P<0.01).Hippocampal Western blot analysis showed that compared with the blank group,the ratios of interleukin(IL)-1β and IL-6 proteins were significantly increased in the model group(P<0.01).Compared with the model group,all dose groups of Guishen Wan significantly reduced the ratios of IL-1β and IL-6 proteins(P<0.01).Compared with the blank group,the ratio of phosphorylated-nuclear transcription factor-κB(p-NF-κB)protein was significantly increased(P<0.01),while the klotho protein was significantly decreased(P<0.01)in the model group.Compared with the model group,all Guishen Wan groups significantly reduced the p-NF-κB protein(P<0.05,P<0.01)and significantly increased the Klotho protein(P<0.01).Conclusion:Guishen Wan effectively ameliorates D-galactose-induced aging in model mice.Its mechanism of action may be related to upregulating Klotho concentration and inhibiting inflammatory factors associated with the NF-κB signaling pathway.
公佩帅;王平
湖北中医药大学,武汉 430065||湖北中医药大学 老年医学研究所,武汉 430065||湖北中医药大学 老年脑健康中医药防护技术与新产品研发教育部工程研究中心,武汉 430065湖北中医药大学,武汉 430065||湖北中医药大学 老年医学研究所,武汉 430065||湖北中医药大学 老年脑健康中医药防护技术与新产品研发教育部工程研究中心,武汉 430065
医药卫生
归肾丸抗衰老克老素蛋白(Klotho)炎症学习记忆
Guishen Wananti-agingKlothoinflammationlearning and memory
《中国实验方剂学杂志》 2026 (19)
13-21,9
湖北省中央引领地方科技发展项目(2020ZYYD021)中医脑健康理论传承创新及应用研究项目(湖北中医药大学2024年度科技创新项目)中医药传承与创新"百千万"人才工程(岐黄工程)——国家中医药领军人才支持计划项目(国中医药人教发[2018]12号)
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