首页|调补心肾方通过活化PI3K/Akt/mTOR通路促进阿尔茨海默病5xFAD转基因小鼠突触可塑性相关蛋白的合成

调补心肾方通过活化PI3K/Akt/mTOR通路促进阿尔茨海默病5xFAD转基因小鼠突触可塑性相关蛋白的合成

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目的 探讨调补心肾方(党参、制首乌、枸杞子、黄芪等)对阿尔茨海默病 5xFAD转基因小鼠突触可塑性的影响及机制.方法 取 5 月龄雄性野生型(WT)小鼠和 5xFAD转基因小鼠各 18 只,分别随机分为对照组(0.9%NaCl)、调补心肾方组(颗粒剂,4.18 g·kg-1)、安理申组(盐酸多奈哌齐,0.625 mg·kg-1),每组 6 只.按照上述分组灌胃给药,每日 1 次,共 60 d.采用透射电镜观察小鼠海马组织超微结构;Western Blot法检测小鼠皮层组织中Synaptophsin、PSD-95、p-NMDAR1、NMDAR1、p-CaMKⅡa、CaMKⅡa、PI3K、p-Akt、Akt、p-mTOR、mTOR蛋白表达水平.结果 与WT对照组比较,5xFAD对照组小鼠海马CA1 区突触的超微结构不规则,线粒体萎缩、减少,线粒体嵴断裂、消失,突触膜弯曲不规则,突触囊泡减少,突触后致密物(PDS)变薄甚至断裂;皮层组织中Synaptophsin、PSD-95、p-NMDAR1/NMDAR1、p-CaMKⅡa/CaMKⅡa、PI3K、p-Akt/Akt、p-mTOR/mTOR蛋白表达均明显下调(P<0.05).与 5xFAD对照组相比较,5xFAD调补心肾方组小鼠海马CA1 区突触的超微结构有明显变化,线粒体数量增加,突触囊泡增多,突触膜完整,突触后致密物有增厚现象;皮层组织中 Synaptophsin、PSD-95、p-NMDAR1/NMDAR1、p-CaMKⅡa/CaMKⅡa、PI3K、p-Akt/Akt、p-mTOR/mTOR蛋白表达明显上调(P<0.05).结论 调补心肾方可能通过活化PI3K/Akt/mTOR通路,促进突触可塑性相关蛋白合成,进而改善AD的认知功能障碍.
Tiaobu Xinshen Prescription Promotes the Synthesis of Synaptic Plasticity-Related Proteins in 5xFAD Transgenic Mice with Alzheimer's Disease by Activating the PI3K/Akt/mTOR Pathway
Objective To investigate the effect and mechanism of Tiaobu Xinshen Prescription(Codonopsis Radix,Polygoni Multiflori Radix Praeparata,Lycii Fructus,Astragali Radix,etc.)on synaptic plasticity in 5xFAD transgenic mice with Alzheimer's disease(AD).Methods Eighteen 5-month-old male wild-type(WT)mice and 18 5xFAD transgenic mice were randomly divided into control group(0.9%NaCl),Tiaobu Xinshen Prescription group(granules,4.18 g·kg-1)and Aricept group(Donepezil Hydrochloride,0.625 mg·kg-1),with six mice in each group.According to the above groups,the rats were given intragastric administration once a day for 60 days.The ultrastructure of hippocampus in mice was observed by transmission electron microscopy.Western Blot was used to detect the protein expression levels of Synaptophsin,PSD-95,p-NMDAR1,NMDAR1,p-CaMKⅡa,CaMKⅡa,PI3K,p-Akt,Akt,p-mTOR and mTOR in mouse cortical tissue.Results Compared with the WT mice control group,the ultrastructure of synapses in the hippocampal CA1 region of the 5xFAD control group was irregular,the mitochondria was atrophied and reduced,the mitochondrial cristae was broken and disappeared,the synaptic membrane was irregularly and curved,the synaptic vesicles were reduced,and the postsynaptic density(PDS)was thinned or even broken.The protein expressions of Synaptophsin,PSD-95,p-NMDAR1/NMDAR1,p-CaMKⅡa/CaMKⅡa,PI3K,p-Akt/Akt and p-mTOR/mTOR in the cortex were significantly down-regulated(P<0.05).Compared with the mice in the 5xFAD control group,the ultrastructure of synapses in the hippocampal CA1 region of the mice in the Tiaobu Xinshen Prescription 5xFAD group was significantly changed,the number of mitochondria was increased,the number of synaptic vesicles was increased,the synaptic membrane was intact,and the postsynaptic density was thickened.The protein expressions of Synaptophsin,PSD-95,p-NMDAR1/NMDAR1,p-CaMKⅡa/CaMKⅡa,PI3K,p-Akt/Akt and p-mTOR/mTOR in the cortex were significantly up-regulated(P<0.05).Conclusion Tiaobu Xinshen Prescription may promote the synthesis of synaptic plasticity-related proteins by activating the PI3K/Akt/mTOR pathway,thereby improving the cognitive dysfunction of AD.

Alzheimer's DiseaseTiaobu Xinshen PrescriptionPI3K/Akt/mTOR signaling pathwaysynaptic plasticity-related proteinscognitive dysfunction5xFAD transgenic mice

林智颖、姚明龙、郑关毅

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福建医科大学附属协和医院,福建 福州 350001

阿尔茨海默病 调补心肾方 PI3K/Akt/mTOR通路 突触可塑性相关蛋白 认知功能障碍 5xFAD转基因小鼠

福建省自然科学基金项目"十四五"非中医医疗机构中医药科室建设项目"十四五"非中医医疗机构中医药科室建设项目第五批医院重点学科建设经费项目

2022J01258212810140121006012022YYZDXK16

2024

中药新药与临床药理
广州中医药大学

中药新药与临床药理

CSTPCD北大核心
影响因子:0.908
ISSN:1003-9783
年,卷(期):2024.35(8)