• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

在阿尔茨海默病的tau转基因模型中,红景天苷通过上调糖原合成酶激酶-3β(GSK-3β)的磷酸化来减少tau蛋白的过度磷酸化。

Salidroside reduces tau hyperphosphorylation via up-regulating GSK-3β phosphorylation in a tau transgenic model of Alzheimer's disease.

作者信息

Zhang Bei, Li Qiongqiong, Chu Xingkun, Sun Suya, Chen Shengdi

机构信息

Department of Neurology and Institute of Neurology, Ruijin Hospital, Shanghai Jiao Tong University School of Medicine, 197 Ruijin Er Road, Shanghai, 200025 China.

Laboratory of Neurodegenerative Diseases, Institute of Health Sciences, Shanghai Institutes for Biological Sciences (SIBS), Chinese Academy of Sciences (CAS) & Shanghai Jiao Tong University School of Medicine (SJTUSM), Shanghai, 200025 China.

出版信息

Transl Neurodegener. 2016 Nov 29;5:21. doi: 10.1186/s40035-016-0068-y. eCollection 2016.

DOI:10.1186/s40035-016-0068-y
PMID:27933142
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5126879/
Abstract

BACKGROUND

Alzheimer's disease (AD) is an age-related and progressive neurodegenerative disease that causes substantial public health care burdens. Intensive efforts have been made to find effective and safe treatment against AD. Salidroside (Sal) is the main effective component of , which has several pharmacological activities. The objective of this study was to investigate the efficacy of Sal in the treatment of AD transgenic and the associated mechanisms.

METHODS

We used tau transgenic line (TAU) in which tau protein is expressed in the central nervous system and eyes by the Gal4/UAS system. After feeding flies with Sal, the lifespan and locomotor activity were recorded. We further examined the appearance of vacuoles in the mushroom body using immunohistochemistry, and detected the levels of total glycogen synthase kinase 3β (t-GSK-3β), phosphorylated GSK-3β (p-GSK-3β), t-tau and p-tau in the brain by western blot analysis.

RESULTS

Our results showed that the longevity was improved in salidroside-fed groups as well as the locomotor activity. We also observed less vacuoles in the mushroom body, upregulated level of p-GSK-3β and downregulated p-tau following Sal treatment.

CONCLUSION

Our data presented the evidence that Sal was capable of reducing the neurodegeneration in tau transgenic and inhibiting neuronal loss. The neuroprotective effects of Sal were associated with its up-regulation of the p-GSK-3β and down-regulation of the p-tau.

摘要

背景

阿尔茨海默病(AD)是一种与年龄相关的进行性神经退行性疾病,给公共卫生保健带来了沉重负担。人们一直在努力寻找有效且安全的AD治疗方法。红景天苷(Sal)是[具体药物名称]的主要有效成分,具有多种药理活性。本研究的目的是探讨红景天苷治疗AD转基因果蝇的疗效及其相关机制。

方法

我们使用tau转基因果蝇品系(TAU),其中tau蛋白通过Gal4/UAS系统在中枢神经系统和眼睛中表达。用红景天苷喂养果蝇后,记录其寿命和运动活性。我们进一步通过免疫组织化学检查蘑菇体中液泡的出现情况,并通过蛋白质免疫印迹分析检测大脑中总糖原合酶激酶3β(t-GSK-3β)、磷酸化GSK-3β(p-GSK-3β)、总tau蛋白(t-tau)和磷酸化tau蛋白(p-tau)的水平。

结果

我们的结果表明,喂食红景天苷的果蝇组寿命延长,运动活性也得到改善。我们还观察到,红景天苷处理后蘑菇体中的液泡减少,p-GSK-3β水平上调,p-tau下调。

结论

我们的数据表明,红景天苷能够减少tau转基因果蝇的神经退行性变并抑制神经元丢失。红景天苷的神经保护作用与其上调p-GSK-3β和下调p-tau有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd0/5126879/1615a417f66c/40035_2016_68_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd0/5126879/17a25e5997fc/40035_2016_68_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd0/5126879/2b7fb4cc4e97/40035_2016_68_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd0/5126879/18cfe123a498/40035_2016_68_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd0/5126879/1615a417f66c/40035_2016_68_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd0/5126879/17a25e5997fc/40035_2016_68_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd0/5126879/2b7fb4cc4e97/40035_2016_68_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd0/5126879/18cfe123a498/40035_2016_68_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bd0/5126879/1615a417f66c/40035_2016_68_Fig4_HTML.jpg

相似文献

1
Salidroside reduces tau hyperphosphorylation via up-regulating GSK-3β phosphorylation in a tau transgenic model of Alzheimer's disease.在阿尔茨海默病的tau转基因模型中,红景天苷通过上调糖原合成酶激酶-3β(GSK-3β)的磷酸化来减少tau蛋白的过度磷酸化。
Transl Neurodegener. 2016 Nov 29;5:21. doi: 10.1186/s40035-016-0068-y. eCollection 2016.
2
Glycogen synthase kinase-3 is associated with neuronal and glial hyperphosphorylated tau deposits in Alzheimer's disease, Pick's disease, progressive supranuclear palsy and corticobasal degeneration.糖原合酶激酶-3与阿尔茨海默病、皮克病、进行性核上性麻痹和皮质基底节变性中的神经元和胶质细胞过度磷酸化tau蛋白沉积有关。
Acta Neuropathol. 2002 Dec;104(6):583-91. doi: 10.1007/s00401-002-0587-8. Epub 2002 Jul 13.
3
Perinatal exposure to lead (Pb) promotes Tau phosphorylation in the rat brain in a GSK-3β and CDK5 dependent manner: Relevance to neurological disorders.围产期铅暴露以依赖糖原合酶激酶-3β(GSK-3β)和细胞周期蛋白依赖性激酶5(CDK5)的方式促进大鼠大脑中的 Tau 蛋白磷酸化:与神经疾病的相关性。
Toxicology. 2016 Mar 10;347-349:17-28. doi: 10.1016/j.tox.2016.03.002. Epub 2016 Mar 21.
4
The active form of glycogen synthase kinase-3beta is associated with granulovacuolar degeneration in neurons in Alzheimer's disease.糖原合酶激酶-3β的活性形式与阿尔茨海默病神经元中的颗粒空泡变性有关。
Acta Neuropathol. 2002 Feb;103(2):91-9. doi: 10.1007/s004010100435. Epub 2001 Nov 29.
5
Truncation and activation of GSK-3β by calpain I: a molecular mechanism links to tau hyperphosphorylation in Alzheimer's disease.钙蛋白酶I对GSK-3β的截断和激活:一种与阿尔茨海默病中tau蛋白过度磷酸化相关的分子机制
Sci Rep. 2015 Feb 2;5:8187. doi: 10.1038/srep08187.
6
Bip enhanced the association of GSK-3β with tau during ER stress both in vivo and in vitro.Bip 在体内和体外增强了 GSK-3β与 tau 在 ER 应激下的结合。
J Alzheimers Dis. 2012;29(4):727-40. doi: 10.3233/JAD-2012-111898.
7
Cornel Iridoid Glycoside Inhibits Tau Hyperphosphorylation via Regulating Cross-Talk Between GSK-3β and PP2A Signaling.山茱萸环烯醚萜苷通过调节GSK-3β与PP2A信号之间的相互作用抑制tau蛋白过度磷酸化。
Front Pharmacol. 2018 Jun 26;9:682. doi: 10.3389/fphar.2018.00682. eCollection 2018.
8
Chronic lithium administration to FTDP-17 tau and GSK-3beta overexpressing mice prevents tau hyperphosphorylation and neurofibrillary tangle formation, but pre-formed neurofibrillary tangles do not revert.长期给携带FTDP-17 tau和过表达糖原合酶激酶3β(GSK-3β)的小鼠施用锂盐可防止tau蛋白过度磷酸化和神经原纤维缠结形成,但预先形成的神经原纤维缠结不会恢复。
J Neurochem. 2006 Dec;99(6):1445-55. doi: 10.1111/j.1471-4159.2006.04139.x. Epub 2006 Oct 24.
9
Stimulatory effect of α-synuclein on the tau-phosphorylation by GSK-3β.α-突触核蛋白对 GSK-3β诱导的 tau 磷酸化的刺激作用。
FEBS J. 2011 Dec;278(24):4895-904. doi: 10.1111/j.1742-4658.2011.08389.x. Epub 2011 Oct 31.
10
Inhibition of glycogen synthase kinase-3β by Angelica sinensis extract decreases β-amyloid-induced neurotoxicity and tau phosphorylation in cultured cortical neurons.当归提取物抑制糖原合酶激酶-3β可减轻β-淀粉样蛋白诱导的皮质神经元的神经毒性和 tau 磷酸化。
J Neurosci Res. 2011 Mar;89(3):437-47. doi: 10.1002/jnr.22563. Epub 2010 Dec 17.

引用本文的文献

1
Natural bioactive compounds form herbal medicine in Alzheimer's disease: from the perspective of GSK-3β.基于糖原合成酶激酶-3β视角探讨天然生物活性化合物在阿尔茨海默病草药治疗中的作用
Front Pharmacol. 2025 Feb 7;16:1497861. doi: 10.3389/fphar.2025.1497861. eCollection 2025.
2
Natural products against tau hyperphosphorylation-induced aggregates: Potential therapies for Alzheimer's disease.针对tau蛋白过度磷酸化诱导的聚集体的天然产物:阿尔茨海默病的潜在疗法。
Arch Pharm (Weinheim). 2025 Jan;358(1):e2400721. doi: 10.1002/ardp.202400721.
3
Natural compounds from herbs and nutraceuticals as glycogen synthase kinase-3β inhibitors in Alzheimer's disease treatment.

本文引用的文献

1
Tau-Centric Targets and Drugs in Clinical Development for the Treatment of Alzheimer's Disease.用于治疗阿尔茨海默病的临床开发中以tau蛋白为核心靶点的药物
Biomed Res Int. 2016;2016:3245935. doi: 10.1155/2016/3245935. Epub 2016 Jun 26.
2
Neuroprotective effects of salidroside through PI3K/Akt pathway activation in Alzheimer's disease models.红景天苷通过激活PI3K/Akt信号通路对阿尔茨海默病模型的神经保护作用
Drug Des Devel Ther. 2016 Apr 6;10:1335-43. doi: 10.2147/DDDT.S99958. eCollection 2016.
3
Effect of Tongxinluo on nerve regeneration in mice with diabetic peripheral neuropathy.
草药和营养保健品中的天然化合物作为糖原合酶激酶-3β抑制剂在阿尔茨海默病治疗中的作用。
CNS Neurosci Ther. 2024 Aug;30(8):e14885. doi: 10.1111/cns.14885.
4
lncRNA and circRNA expression profiles in the hippocampus of Aβ‑induced AD mice treated with Tripterygium glycoside.雷公藤多苷治疗的Aβ诱导AD小鼠海马中的长链非编码RNA和环状RNA表达谱
Exp Ther Med. 2023 Jul 19;26(3):426. doi: 10.3892/etm.2023.12125. eCollection 2023 Sep.
5
Evaluation of a Newly Synthesized Acetylcholinesterase Inhibitor in a Transgenic Model of Alzheimer's Disease.在阿尔茨海默病转基因模型中对一种新合成的乙酰胆碱酯酶抑制剂的评估。
Front Neurosci. 2021 Jun 30;15:691222. doi: 10.3389/fnins.2021.691222. eCollection 2021.
6
Salidroside Attenuates Cognitive Dysfunction in Senescence-Accelerated Mouse Prone 8 (SAMP8) Mice and Modulates Inflammation of the Gut-Brain Axis.红景天苷减轻衰老加速小鼠易感8型(SAMP8)小鼠的认知功能障碍并调节肠-脑轴炎症。
Front Pharmacol. 2020 Dec 9;11:568423. doi: 10.3389/fphar.2020.568423. eCollection 2020.
7
Pharmacological Treatment of Alzheimer's Disease: Insights from .阿尔茨海默病的药物治疗:. 的见解
Int J Mol Sci. 2020 Jun 29;21(13):4621. doi: 10.3390/ijms21134621.
8
GRP78/BIP/HSPA5 as a Therapeutic Target in Models of Parkinson's Disease: A Mini Review.GRP78/BIP/HSPA5作为帕金森病模型中的治疗靶点:一篇综述
Adv Pharmacol Sci. 2019 Mar 5;2019:2706783. doi: 10.1155/2019/2706783. eCollection 2019.
9
Rosenroot (): Potential Applications in Aging-related Diseases.迷迭香叶:在衰老相关疾病中的潜在应用。
Aging Dis. 2019 Feb 1;10(1):134-146. doi: 10.14336/AD.2018.0511. eCollection 2019 Feb.
10
Ellagic acid ameliorates learning and memory impairment in APP/PS1 transgenic mice via inhibition of β-amyloid production and tau hyperphosphorylation.鞣花酸通过抑制β-淀粉样蛋白生成和tau蛋白过度磷酸化改善APP/PS1转基因小鼠的学习和记忆障碍。
Exp Ther Med. 2018 Dec;16(6):4951-4958. doi: 10.3892/etm.2018.6860. Epub 2018 Oct 15.
Cell Mol Biol (Noisy-le-grand). 2015 Oct 30;61(5):103-7.
4
Salidroside ameliorates cognitive impairment in a d-galactose-induced rat model of Alzheimer's disease.红景天苷改善D-半乳糖诱导的阿尔茨海默病大鼠模型的认知障碍。
Behav Brain Res. 2015 Oct 15;293:27-33. doi: 10.1016/j.bbr.2015.06.045. Epub 2015 Jul 17.
5
Salidroside protects retinal endothelial cells against hydrogen peroxide-induced injury via modulating oxidative status and apoptosis.红景天苷通过调节氧化状态和细胞凋亡来保护视网膜内皮细胞免受过氧化氢诱导的损伤。
Biosci Biotechnol Biochem. 2015;79(9):1406-13. doi: 10.1080/09168451.2015.1038212. Epub 2015 Apr 29.
6
Optimization on Preparation Conditions of Salidroside Liposome and Its Immunological Activity on PCV-2 in Mice.红景天苷脂质体的制备条件优化及其对小鼠猪圆环病毒2型的免疫活性
Evid Based Complement Alternat Med. 2015;2015:178128. doi: 10.1155/2015/178128. Epub 2015 Mar 23.
7
Salidroside inhibits the growth of human breast cancer in vitro and in vivo.红景天苷在体外和体内均可抑制人乳腺癌的生长。
Oncol Rep. 2015 May;33(5):2553-60. doi: 10.3892/or.2015.3857. Epub 2015 Mar 17.
8
Cellular Models of Aggregation-dependent Template-directed Proteolysis to Characterize Tau Aggregation Inhibitors for Treatment of Alzheimer Disease.用于表征治疗阿尔茨海默病的tau聚集抑制剂的聚集依赖性模板导向蛋白水解的细胞模型
J Biol Chem. 2015 Apr 24;290(17):10862-75. doi: 10.1074/jbc.M114.616029. Epub 2015 Mar 10.
9
The combination of aricept with a traditional Chinese medicine formula, smart soup, may be a novel way to treat Alzheimer's disease.安理申与一种中药配方——益智汤联合使用,可能是治疗阿尔茨海默病的一种新方法。
J Alzheimers Dis. 2015;45(4):1185-95. doi: 10.3233/JAD-143183.
10
Salidroside rescued mice from experimental sepsis through anti-inflammatory and anti-apoptosis effects.红景天苷通过抗炎和抗凋亡作用使小鼠免受实验性败血症的侵害。
J Surg Res. 2015 May 1;195(1):277-83. doi: 10.1016/j.jss.2015.01.021. Epub 2015 Jan 14.