• 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

神经退行性疾病中的胆汁酸

Bile Acids in Neurodegenerative Disorders.

作者信息

Ackerman Hayley D, Gerhard Glenn S

机构信息

Department of Medical Genetics and Molecular Biochemistry, The Lewis Katz School of Medicine at Temple University Philadelphia, PA, USA.

出版信息

Front Aging Neurosci. 2016 Nov 22;8:263. doi: 10.3389/fnagi.2016.00263. eCollection 2016.

DOI:10.3389/fnagi.2016.00263
PMID:27920719
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5118426/
Abstract

Bile acids, a structurally related group of molecules derived from cholesterol, have a long history as therapeutic agents in medicine, from treatment for primarily ocular diseases in ancient Chinese medicine to modern day use as approved drugs for certain liver diseases. Despite evidence supporting a neuroprotective role in a diverse spectrum of age-related neurodegenerative disorders, including several small pilot clinical trials, little is known about their molecular mechanisms or their physiological roles in the nervous system. We review the data reported for their use as treatments for neurodegenerative diseases and their underlying molecular basis. While data from cellular and animal models and clinical trials support potential efficacy to treat a variety of neurodegenerative disorders, the relevant bile acids, their origin, and the precise molecular mechanism(s) by which they confer neuroprotection are not known delaying translation to the clinical setting.

摘要

胆汁酸是一类结构相关的分子,由胆固醇衍生而来,作为治疗药物在医学领域有着悠久的历史,从古代中医主要用于治疗眼部疾病到现代作为某些肝脏疾病的获批药物。尽管有证据支持胆汁酸在多种与年龄相关的神经退行性疾病中具有神经保护作用,包括几项小型先导性临床试验,但对于它们在神经系统中的分子机制或生理作用却知之甚少。我们综述了有关胆汁酸用于治疗神经退行性疾病及其潜在分子基础的报道数据。虽然来自细胞和动物模型以及临床试验的数据支持其治疗多种神经退行性疾病的潜在疗效,但相关的胆汁酸、它们的来源以及它们赋予神经保护作用的确切分子机制尚不清楚,这延缓了其向临床应用的转化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a1/5118426/bd18f929050f/fnagi-08-00263-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a1/5118426/e0162a8aff6c/fnagi-08-00263-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a1/5118426/bd18f929050f/fnagi-08-00263-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a1/5118426/e0162a8aff6c/fnagi-08-00263-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40a1/5118426/bd18f929050f/fnagi-08-00263-g0002.jpg

相似文献

1
Bile Acids in Neurodegenerative Disorders.神经退行性疾病中的胆汁酸
Front Aging Neurosci. 2016 Nov 22;8:263. doi: 10.3389/fnagi.2016.00263. eCollection 2016.
2
Mitochondrial biogenesis: pharmacological approaches.线粒体生物合成:药理学方法。
Curr Pharm Des. 2014;20(35):5507-9. doi: 10.2174/138161282035140911142118.
3
Impacts of methylxanthines and adenosine receptors on neurodegeneration: human and experimental studies.甲基黄嘌呤和腺苷受体对神经退行性变的影响:人体及实验研究
Handb Exp Pharmacol. 2011(200):267-310. doi: 10.1007/978-3-642-13443-2_10.
4
Bile Acids Reduce Prion Conversion, Reduce Neuronal Loss, and Prolong Male Survival in Models of Prion Disease.胆汁酸可减少朊病毒转化、减少神经元损失并延长朊病毒病模型中雄性动物的生存期。
J Virol. 2015 Aug;89(15):7660-72. doi: 10.1128/JVI.01165-15.
5
Repurposing of Copper(II)-chelating Drugs for the Treatment of Neurodegenerative Diseases.重新利用铜(II)螯合药物治疗神经退行性疾病。
Curr Med Chem. 2018 Feb 12;25(4):525-539. doi: 10.2174/0929867324666170518094404.
6
Exosomes as a potential novel therapeutic tools against neurodegenerative diseases.外泌体作为一种针对神经退行性疾病的潜在新型治疗工具。
Pharmacol Res. 2016 Nov;113(Pt B):816-822. doi: 10.1016/j.phrs.2016.02.002. Epub 2016 Feb 6.
7
Chinese Medicine: A Hope for Neurodegenerative Diseases?中医:神经退行性疾病的希望?
J Alzheimers Dis. 2017;60(s1):S151-S160. doi: 10.3233/JAD-170374.
8
Bile acids and bile acid derivatives: use in drug delivery systems and as therapeutic agents.胆汁酸和胆汁酸衍生物:在药物传递系统和治疗剂中的应用。
Expert Opin Drug Deliv. 2016 Aug;13(8):1133-48. doi: 10.1080/17425247.2016.1178233. Epub 2016 May 2.
9
Sigma-1 Receptors and Neurodegenerative Diseases: Towards a Hypothesis of Sigma-1 Receptors as Amplifiers of Neurodegeneration and Neuroprotection.西格玛-1受体与神经退行性疾病:关于西格玛-1受体作为神经退行性变和神经保护放大器的假说
Adv Exp Med Biol. 2017;964:133-152. doi: 10.1007/978-3-319-50174-1_10.
10
The Neuroprotective Effect of Doxycycline on Neurodegenerative Diseases.强力霉素对神经退行性疾病的神经保护作用。
Neurotox Res. 2019 May;35(4):981-986. doi: 10.1007/s12640-019-00015-z. Epub 2019 Feb 23.

引用本文的文献

1
Bile Acid Metabolism Changes in Patients with a -Associated Inherited Retinal Degeneration.α-相关遗传性视网膜变性患者的胆汁酸代谢变化
Ophthalmol Sci. 2025 Jan 7;5(4):100704. doi: 10.1016/j.xops.2025.100704. eCollection 2025 Jul-Aug.
2
Fecal Microbial Profiles and Short-Chain Fatty Acid/Bile Acid Metabolomics in Patients With Age-Related Macular Degeneration: A Pilot Study.年龄相关性黄斑变性患者的粪便微生物谱及短链脂肪酸/胆汁酸代谢组学:一项初步研究
Invest Ophthalmol Vis Sci. 2025 Apr 1;66(4):21. doi: 10.1167/iovs.66.4.21.
3
Bile acid receptors and signaling crosstalk in the liver, gut and brain.

本文引用的文献

1
Rexinoids as Therapeutics for Alzheimer's Disease: Role of APOE.视黄酸类化合物作为阿尔茨海默病的治疗药物:载脂蛋白E的作用
Curr Top Med Chem. 2017;17(6):708-720. doi: 10.2174/1568026616666160617090227.
2
Cellular and circuit mechanisms underlying spinocerebellar ataxias.脊髓小脑共济失调的细胞和环路机制
J Physiol. 2016 Aug 15;594(16):4653-60. doi: 10.1113/JP271897. Epub 2016 Jun 12.
3
Bile salts in control of lipid metabolism.胆汁盐对脂质代谢的调控作用。
肝脏、肠道和大脑中的胆汁酸受体与信号转导串扰
Liver Res. 2021 Jul 18;5(3):105-118. doi: 10.1016/j.livres.2021.07.002. eCollection 2021 Sep.
4
The effects of ursodeoxycholic acid on Parkinson's disease, a mechanistic review of the recent evidence.熊去氧胆酸对帕金森病的影响:近期证据的机制性综述
Metab Brain Dis. 2025 Feb 1;40(2):115. doi: 10.1007/s11011-025-01542-9.
5
Non-Categorical Analyses Identify Rotenone-Induced 'Parkinsonian' Rats Benefiting from Nano-Emulsified Punicic Acid (Nano-PSO) in a Phenotypically Diverse Population: Implications for Translational Neurodegenerative Therapies.非分类分析表明,在表型多样的群体中,鱼藤酮诱导的“帕金森病”大鼠可从纳米乳化石榴酸(纳米PSO)中获益:对转化神经退行性疾病治疗的启示。
Int J Mol Sci. 2024 Nov 25;25(23):12635. doi: 10.3390/ijms252312635.
6
The bile acid chenodeoxycholic acid associates with reduced stroke in humans and mice.胆汁酸鹅去氧胆酸与人类和小鼠中风风险降低有关。
J Lipid Res. 2025 Jan;66(1):100712. doi: 10.1016/j.jlr.2024.100712. Epub 2024 Nov 21.
7
Diagnostic Potential of Alternations of Bile Acid Profiles in the Plasma of Patients with Huntington's Disease.亨廷顿舞蹈症患者血浆胆汁酸谱变化的诊断潜力
Metabolites. 2024 Jul 20;14(7):394. doi: 10.3390/metabo14070394.
8
Tauroursodeoxycholic acid: a bile acid that may be used for the prevention and treatment of Alzheimer's disease.牛磺熊去氧胆酸:一种可用于预防和治疗阿尔茨海默病的胆汁酸。
Front Neurosci. 2024 Feb 19;18:1348844. doi: 10.3389/fnins.2024.1348844. eCollection 2024.
9
The microbiota-gut-brain axis in Huntington's disease: pathogenic mechanisms and therapeutic targets.亨廷顿舞蹈病中的微生物群-肠-脑轴:致病机制与治疗靶点
FEBS J. 2025 Mar;292(6):1282-1315. doi: 10.1111/febs.17102. Epub 2024 Mar 1.
10
Integration of plasma and CSF metabolomics with CSF proteomic reveals novel associations between lipid mediators and central nervous system vascular and energy metabolism.血浆和脑脊液代谢组学与脑脊液蛋白质组学的整合揭示了脂质介质与中枢神经系统血管和能量代谢之间的新关联。
Sci Rep. 2023 Aug 23;13(1):13752. doi: 10.1038/s41598-023-39737-8.
Curr Opin Lipidol. 2016 Jun;27(3):295-301. doi: 10.1097/MOL.0000000000000303.
4
Alzheimer's disease.阿尔茨海默病。
Lancet. 2016 Jul 30;388(10043):505-17. doi: 10.1016/S0140-6736(15)01124-1. Epub 2016 Feb 24.
5
Therapeutic potential of Takeda-G-protein-receptor-5 (TGR5) agonists. Hope or hype?武田-G 蛋白偶联受体 5(TGR5)激动剂的治疗潜力:希望还是炒作?
Diabetes Obes Metab. 2016 May;18(5):439-43. doi: 10.1111/dom.12636. Epub 2016 Mar 17.
6
Retinoids and motor neuron disease: Potential role in amyotrophic lateral sclerosis.维甲酸与运动神经元疾病:在肌萎缩侧索硬化症中的潜在作用。
J Neurol Sci. 2016 Jan 15;360:115-20. doi: 10.1016/j.jns.2015.11.058. Epub 2015 Dec 2.
7
Genetic Variants in MicroRNAs and Their Binding Sites Are Associated with the Risk of Parkinson Disease.微小RNA及其结合位点的基因变异与帕金森病风险相关。
Hum Mutat. 2016 Mar;37(3):292-300. doi: 10.1002/humu.22943. Epub 2015 Dec 31.
8
JNK-mediated activation of ATF2 contributes to dopaminergic neurodegeneration in the MPTP mouse model of Parkinson's disease.JNK介导的ATF2激活促成帕金森病MPTP小鼠模型中的多巴胺能神经变性。
Exp Neurol. 2016 Mar;277:296-304. doi: 10.1016/j.expneurol.2015.10.010. Epub 2015 Oct 26.
9
Effects of Tauroursodeoxycholic Acid and Alpha-Lipoic-Acid on the Visual Response Properties of Cat Retinal Ganglion Cells: An In Vitro Study.牛磺熊去氧胆酸和α-硫辛酸对猫视网膜神经节细胞视觉反应特性的影响:一项体外研究
Invest Ophthalmol Vis Sci. 2015 Oct;56(11):6638-45. doi: 10.1167/iovs.15-17301.
10
Neuroprotective Effect of Tauroursodeoxycholic Acid on N-Methyl-D-Aspartate-Induced Retinal Ganglion Cell Degeneration.牛磺熊去氧胆酸对N-甲基-D-天冬氨酸诱导的视网膜神经节细胞变性的神经保护作用
PLoS One. 2015 Sep 17;10(9):e0137826. doi: 10.1371/journal.pone.0137826. eCollection 2015.