An interventional study of baicalin on neuronal pentraxin-1, neuronal pentraxin-2, and C-reactive protein in Alzheimer's disease rat model.

IF 1.8 4区 医学 Q4 NEUROSCIENCES
Jing-Kun Zhao, Si-Jia Hou, Ji-Wei Zhao, Hong-Li Yu, Shu-Rong Duan
{"title":"An interventional study of baicalin on neuronal pentraxin-1, neuronal pentraxin-2, and C-reactive protein in Alzheimer's disease rat model.","authors":"Jing-Kun Zhao,&nbsp;Si-Jia Hou,&nbsp;Ji-Wei Zhao,&nbsp;Hong-Li Yu,&nbsp;Shu-Rong Duan","doi":"10.1515/tnsci-2022-0298","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Baicalin has been shown to promote spatial learning and neural regeneration, which might increase the differentiation of neural stem cells in Alzheimer's disease (AD) rat models. We aimed to study the role of baicalin on neuronal pentraxin-1 (NPTX-1), neuronal pentraxin-2 (NPTX-2), and C-reactive protein (CRP) in AD model rats.</p><p><strong>Methods: </strong>The 30 male Sprague Dawley rats were divided into three groups: the control group, the AD model group, and the AD + baicalin group. Then, the Morris water maze was used to verify the effect of baicalin on the memory and spatial learning of rats. Immunohistochemistry and immunofluorescence were used to observe the expression of NPTX-1, NPTX-2, and CRP in brain tissue.</p><p><strong>Results: </strong>Compared with the AD model group, the AD rats treated with baicalin spent significantly less time finding escape latencies (<i>P</i> = 0.008) and had longer cross-platform times in the target quadrant (<i>P</i> = 0.015). In addition, the AD + baicalin group had significantly higher numbers of hippocampal neurons compared with the AD model group (<i>P</i> < 0.05). Baicalin also obviously decreased the apoptosis of neurons. Moreover, compared with the AD model group, the NPTX-1 and CRP expression in the AD + baicalin group was significantly reduced (<i>P</i> = 0.000) while the expression of NPTX-2 in the brain tissue of AD rats was significantly increased (<i>P</i> = 0.000).</p><p><strong>Conclusions: </strong>Baicalin can play a therapeutic role by downregulating NPTX-1, upregulating NPTX-2, and downregulating CPR in AD model rats.</p>","PeriodicalId":23227,"journal":{"name":"Translational Neuroscience","volume":null,"pages":null},"PeriodicalIF":1.8000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10500638/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Translational Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1515/tnsci-2022-0298","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Baicalin has been shown to promote spatial learning and neural regeneration, which might increase the differentiation of neural stem cells in Alzheimer's disease (AD) rat models. We aimed to study the role of baicalin on neuronal pentraxin-1 (NPTX-1), neuronal pentraxin-2 (NPTX-2), and C-reactive protein (CRP) in AD model rats.

Methods: The 30 male Sprague Dawley rats were divided into three groups: the control group, the AD model group, and the AD + baicalin group. Then, the Morris water maze was used to verify the effect of baicalin on the memory and spatial learning of rats. Immunohistochemistry and immunofluorescence were used to observe the expression of NPTX-1, NPTX-2, and CRP in brain tissue.

Results: Compared with the AD model group, the AD rats treated with baicalin spent significantly less time finding escape latencies (P = 0.008) and had longer cross-platform times in the target quadrant (P = 0.015). In addition, the AD + baicalin group had significantly higher numbers of hippocampal neurons compared with the AD model group (P < 0.05). Baicalin also obviously decreased the apoptosis of neurons. Moreover, compared with the AD model group, the NPTX-1 and CRP expression in the AD + baicalin group was significantly reduced (P = 0.000) while the expression of NPTX-2 in the brain tissue of AD rats was significantly increased (P = 0.000).

Conclusions: Baicalin can play a therapeutic role by downregulating NPTX-1, upregulating NPTX-2, and downregulating CPR in AD model rats.

Abstract Image

Abstract Image

Abstract Image

黄芩苷对阿尔茨海默病大鼠模型神经元戊烷素-1、戊烷素-2及c反应蛋白的干预研究。
背景:黄芩苷有促进空间学习和神经再生的作用,这可能会增加阿尔茨海默病(AD)大鼠神经干细胞的分化。本实验旨在研究黄芩苷对AD模型大鼠神经元戊烷素-1 (NPTX-1)、神经元戊烷素-2 (NPTX-2)和c反应蛋白(CRP)的影响。方法:将30只雄性sd大鼠分为对照组、AD模型组和AD +黄芩苷组。然后采用Morris水迷宫验证黄芩苷对大鼠记忆和空间学习的影响。采用免疫组织化学和免疫荧光法观察NPTX-1、NPTX-2、CRP在脑组织中的表达。结果:与AD模型组比较,黄芩苷组AD大鼠寻找逃避潜伏期的时间明显缩短(P = 0.008),目标象限的跨平台时间明显延长(P = 0.015)。AD +黄芩苷组海马神经元数量显著高于AD模型组(P < 0.05)。黄芩苷还能明显减少神经元的凋亡。与AD模型组比较,AD +黄芩苷组AD大鼠脑组织中NPTX-1和CRP的表达明显降低(P = 0.000), NPTX-2的表达明显升高(P = 0.000)。结论:黄芩苷可能通过下调NPTX-1、上调NPTX-2、下调CPR对AD模型大鼠有治疗作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
CiteScore
3.00
自引率
4.80%
发文量
45
审稿时长
>12 weeks
期刊介绍: Translational Neuroscience provides a closer interaction between basic and clinical neuroscientists to expand understanding of brain structure, function and disease, and translate this knowledge into clinical applications and novel therapies of nervous system disorders.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信