• 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

月见草和贯叶连翘提取物对实验性自身免疫性脑脊髓炎小鼠某些中枢神经系统髓鞘蛋白、脑组织病理学及氧化应激的影响

Effects of Oenothera biennis L. and Hypericum perforatum L. extracts on some central nervous system myelin proteins, brain histopathology and oxidative stress in mice with experimental autoimmune encephalomyelitis.

作者信息

Selek S, Esrefoglu M, Meral I, Bulut H, Caglar H G, Sonuc G, Yildiz C, Teloglu E S, Dogan N, Yuce B, Tiftik E, Bayindir N

机构信息

a Departments of Medical Biochemistry , Bezmialem Vakif University , Istanbul , Turkey.

b Histology and Embryology , Bezmialem Vakif University , Istanbul , Turkey.

出版信息

Biotech Histochem. 2019 Feb;94(2):75-83. doi: 10.1080/10520295.2018.1482001. Epub 2019 Apr 8.

DOI:10.1080/10520295.2018.1482001
PMID:30957550
Abstract

We investigated the effects of Oenothera biennis L. and Hypericum perforatum L. extracts on brain tissue histopathology, myelin oligodendrocyte glycoprotein (MOG), myelin basic protein (MBP), total antioxidant status (TAS), total oxidant status (TOS) and oxidative stress index (OSI) in mice with experimental autoimmune encephalomyelitis (EAE). Forty-seven C57BL/6J mice were divided into the following groups: multiple sclerosis (MS), control (healthy mice), MS + H. perforatum treated (MS + HP), MS + O. biennis treated (MS + OB). All groups except the control group were immunized by EAE methods. Two weeks after the immunization, the mice in the MS + HP group were fed normal food containing 18 - 21 g/kg H. perforatum extract, the mice in MS + OB group were fed normal food containing 18 - 21 g/kg O. biennis extract, and the mice in control and MS groups were fed normal food for six weeks. Brain tissue samples were collected from all mice for histopathological and biochemical analysis. Clinical signs of the disease were scored using functional systems scores (FSS) daily. The H. perforatum and O. biennis extracts ameliorated the increased brain tissue MOG and MBP values for animals with MS. H. perforatum and O. biennis extract decreased the TOS and OSI values for brain tissue and increased TAS levels in brain tissue of animals with MS. In addition, H. perforatum and O. biennis extracts decreased the clinical signs at the end of the experiment compared to the beginning of extract administration. We found that myelin was lost in MS group vs. control group. H. perforatum and O. biennis extract treatments decreased the amount of myelin loss in the MS + HP and MS + OB groups. We also observed amyloid deposition on vascular walls, in the cytoplasm of the neurons and in the intercellular space in the MS group. O. biennis and H. perforatum treated groups exhibited neither abnormal amyloid deposition nor obvious cell infiltration. The beneficial effects of O. biennis and H. perforatum for attenuating myelin loss and amyloid deposition suggest their therapeutic utility for treatment of MS.

摘要

我们研究了月见草和贯叶连翘提取物对实验性自身免疫性脑脊髓炎(EAE)小鼠脑组织组织病理学、髓鞘少突胶质细胞糖蛋白(MOG)、髓鞘碱性蛋白(MBP)、总抗氧化状态(TAS)、总氧化状态(TOS)和氧化应激指数(OSI)的影响。47只C57BL/6J小鼠被分为以下几组:多发性硬化症(MS)组、对照组(健康小鼠)、MS + 贯叶连翘治疗组(MS + HP)、MS + 月见草治疗组(MS + OB)。除对照组外,所有组均采用EAE方法进行免疫。免疫两周后,MS + HP组的小鼠喂食含18 - 21 g/kg贯叶连翘提取物的正常食物,MS + OB组的小鼠喂食含18 - 21 g/kg月见草提取物的正常食物,对照组和MS组的小鼠喂食正常食物六周。从所有小鼠收集脑组织样本进行组织病理学和生化分析。每天使用功能系统评分(FSS)对疾病的临床症状进行评分。贯叶连翘和月见草提取物改善了MS动物脑组织中升高的MOG和MBP值。贯叶连翘和月见草提取物降低了脑组织的TOS和OSI值,并提高了MS动物脑组织中的TAS水平。此外,与提取物给药开始时相比,贯叶连翘和月见草提取物在实验结束时降低了临床症状。我们发现MS组与对照组相比髓鞘丢失。贯叶连翘和月见草提取物治疗减少了MS + HP组和MS + OB组的髓鞘丢失量。我们还观察到MS组血管壁、神经元细胞质和细胞间隙中有淀粉样沉积。月见草和贯叶连翘治疗组既没有异常的淀粉样沉积也没有明显的细胞浸润。月见草和贯叶连翘对减轻髓鞘丢失和淀粉样沉积的有益作用表明它们在治疗MS方面的治疗效用。

相似文献

1
Effects of Oenothera biennis L. and Hypericum perforatum L. extracts on some central nervous system myelin proteins, brain histopathology and oxidative stress in mice with experimental autoimmune encephalomyelitis.月见草和贯叶连翘提取物对实验性自身免疫性脑脊髓炎小鼠某些中枢神经系统髓鞘蛋白、脑组织病理学及氧化应激的影响
Biotech Histochem. 2019 Feb;94(2):75-83. doi: 10.1080/10520295.2018.1482001. Epub 2019 Apr 8.
2
St. John's wort and its component hyperforin alleviate experimental autoimmune encephalomyelitis through expansion of regulatory T-cells.圣约翰草及其成分金丝桃素通过调节性T细胞的扩增减轻实验性自身免疫性脑脊髓炎。
J Immunotoxicol. 2016 May;13(3):364-74. doi: 10.3109/1547691X.2015.1101512. Epub 2015 Dec 3.
3
Mice overexpressing Bcl-2 in their neurons are resistant to myelin oligodendrocyte glycoprotein (MOG)-induced experimental autoimmune encephalomyelitis (EAE).神经元中过表达Bcl-2的小鼠对髓鞘少突胶质细胞糖蛋白(MOG)诱导的实验性自身免疫性脑脊髓炎(EAE)具有抗性。
J Mol Neurosci. 2000 Dec;15(3):167-76. doi: 10.1385/JMN:15:3:167.
4
Early axonal damage and progressive myelin pathology define the kinetics of CNS histopathology in a mouse model of multiple sclerosis.早期轴突损伤和进行性髓鞘病理改变定义了多发性硬化症小鼠模型中枢神经系统组织病理学的动力学特征。
Clin Immunol. 2013 Oct;149(1):32-45. doi: 10.1016/j.clim.2013.06.004. Epub 2013 Jun 18.
5
Lentivirus-mediated estrogen receptor α overexpression in the central nervous system ameliorates experimental autoimmune encephalomyelitis in mice.慢病毒介导的中枢神经系统雌激素受体 α 过表达可改善实验性自身免疫性脑脊髓炎小鼠的病情。
Int J Mol Med. 2013 May;31(5):1209-21. doi: 10.3892/ijmm.2013.1306. Epub 2013 Mar 15.
6
Time-Dependent Progression of Demyelination and Axonal Pathology in MP4-Induced Experimental Autoimmune Encephalomyelitis.MP4诱导的实验性自身免疫性脑脊髓炎中脱髓鞘和轴突病理的时间依赖性进展
PLoS One. 2015 Dec 11;10(12):e0144847. doi: 10.1371/journal.pone.0144847. eCollection 2015.
7
Steroid protection in the experimental autoimmune encephalomyelitis model of multiple sclerosis.类固醇在多发性硬化症实验性自身免疫性脑脊髓炎模型中的保护作用。
Neuroimmunomodulation. 2008;15(1):76-83. doi: 10.1159/000135627. Epub 2008 Jul 29.
8
Alterations of peripheral nerve excitability in an experimental autoimmune encephalomyelitis mouse model for multiple sclerosis.实验性自身免疫性脑脊髓炎多发性硬化症模型小鼠周围神经兴奋性改变。
J Neuroinflammation. 2020 Sep 7;17(1):266. doi: 10.1186/s12974-020-01936-9.
9
MOG extracellular domain (p1-125) triggers elevated frequency of CXCR3+ CD4+ Th1 cells in the CNS of mice and induces greater incidence of severe EAE.MOG 细胞外结构域 (p1-125) 可引发小鼠中枢神经系统中 CXCR3+ CD4+ Th1 细胞的频率升高,并导致更严重的 EAE 发生率增加。
Mult Scler. 2014 Sep;20(10):1312-21. doi: 10.1177/1352458514524086. Epub 2014 Feb 19.
10
Experimental Autoimmune Encephalomyelitis (EAE) Model of Cynomolgus Macaques Induced by Recombinant Human MOG1-125 (rhMOG1-125) Protein and MOG34-56 Peptide.重组人MOG1-125(rhMOG1-125)蛋白和MOG34-56肽诱导食蟹猴实验性自身免疫性脑脊髓炎(EAE)模型
Protein Pept Lett. 2018 Feb 8;24(12):1166-1178. doi: 10.2174/0929866524666171110093626.

引用本文的文献

1
Environmental selection underlies distinct distribution patterns of closely related European evening primroses.环境选择是亲缘关系相近的欧洲月见草呈现不同分布模式的基础。
Sci Rep. 2025 Feb 5;15(1):4436. doi: 10.1038/s41598-025-88888-3.
2
Antioxidant Therapies in the Treatment of Multiple Sclerosis.抗氧化疗法治疗多发性硬化症。
Biomolecules. 2024 Oct 8;14(10):1266. doi: 10.3390/biom14101266.
3
Potential Utility of Natural Products against Oxidative Stress in Animal Models of Multiple Sclerosis.天然产物在多发性硬化症动物模型中对抗氧化应激的潜在效用
Antioxidants (Basel). 2022 Jul 29;11(8):1495. doi: 10.3390/antiox11081495.