Symbiotic Supplementation (E. faecium and Agave Inulin) Improves Spatial Memory and Increases Plasticity in the Hippocampus of Obese Rats: A Proof-of-Concept Study.

IF 3.2 4区 医学 Q3 CELL & TISSUE ENGINEERING Cell Transplantation Pub Date : 2023-01-01 DOI:10.1177/09636897231177357
Alejandra Romo-Araiza, Rocío I Picazo-Aguilar, Ernesto Griego, Luis A Márquez, Emilio J Galván, Yolanda Cruz, Ana María Fernández-Presas, Almudena Chávez-Guerra, Roxana Rodríguez-Barrera, Ana P Azpiri-Cardós, Claudia Rosas-Quintero, Ricardo Jasso-Chávez, Cesar V Borlongan, Antonio Ibarra
{"title":"Symbiotic Supplementation (<i>E. faecium</i> and Agave Inulin) Improves Spatial Memory and Increases Plasticity in the Hippocampus of Obese Rats: A Proof-of-Concept Study.","authors":"Alejandra Romo-Araiza,&nbsp;Rocío I Picazo-Aguilar,&nbsp;Ernesto Griego,&nbsp;Luis A Márquez,&nbsp;Emilio J Galván,&nbsp;Yolanda Cruz,&nbsp;Ana María Fernández-Presas,&nbsp;Almudena Chávez-Guerra,&nbsp;Roxana Rodríguez-Barrera,&nbsp;Ana P Azpiri-Cardós,&nbsp;Claudia Rosas-Quintero,&nbsp;Ricardo Jasso-Chávez,&nbsp;Cesar V Borlongan,&nbsp;Antonio Ibarra","doi":"10.1177/09636897231177357","DOIUrl":null,"url":null,"abstract":"<p><p>Obesity has been linked to cognitive impairment through systemic low-grade inflammation. High fat and sugar diets (HFSDs) also induce systemic inflammation, either by induced Toll-like receptor 4 response, or by causing dysbiosis. This study aimed to evaluate the effect of symbiotics supplementation on spatial and working memory, butyrate concentration, neurogenesis, and electrophysiological recovery of HFSD-fed rats. In a first experiment, Sprague-Dawley male rats were given HFSD for 10 weeks, after which they were randomized into 2 groups (<i>n</i> = 10 per group): water (control), or <i>Enterococcus faecium</i> + inulin (symbiotic) administration, for 5 weeks. In the fifth week, spatial and working memory was analyzed through the Morris Water Maze (MWM) and Eight-Arm Radial Maze (RAM) tests, respectively, with 1 week apart between tests. At the end of the study, butyrate levels from feces and neurogenesis at hippocampus were determined. In a second experiment with similar characteristics, the hippocampus was extracted to perform electrophysiological studies. Symbiotic-supplemented rats showed a significantly better memory, butyrate concentrations, and neurogenesis. This group also presented an increased firing frequency in hippocampal neurons [and a larger <i>N</i>-methyl-d-aspartate (NMDA)/α-amino-3-hydroxyl-5-methyl-4-isoxazole-propionate (AMPA) current ratio] suggesting an increase in NMDA receptors, which in turn is associated with an enhancement in long-term potentiation and synaptic plasticity. Therefore, our results suggest that symbiotics could restore obesity-related memory impairment and promote synaptic plasticity.</p>","PeriodicalId":9721,"journal":{"name":"Cell Transplantation","volume":"32 ","pages":"9636897231177357"},"PeriodicalIF":3.2000,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/7f/8e/10.1177_09636897231177357.PMC10272678.pdf","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cell Transplantation","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1177/09636897231177357","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CELL & TISSUE ENGINEERING","Score":null,"Total":0}
引用次数: 1

Abstract

Obesity has been linked to cognitive impairment through systemic low-grade inflammation. High fat and sugar diets (HFSDs) also induce systemic inflammation, either by induced Toll-like receptor 4 response, or by causing dysbiosis. This study aimed to evaluate the effect of symbiotics supplementation on spatial and working memory, butyrate concentration, neurogenesis, and electrophysiological recovery of HFSD-fed rats. In a first experiment, Sprague-Dawley male rats were given HFSD for 10 weeks, after which they were randomized into 2 groups (n = 10 per group): water (control), or Enterococcus faecium + inulin (symbiotic) administration, for 5 weeks. In the fifth week, spatial and working memory was analyzed through the Morris Water Maze (MWM) and Eight-Arm Radial Maze (RAM) tests, respectively, with 1 week apart between tests. At the end of the study, butyrate levels from feces and neurogenesis at hippocampus were determined. In a second experiment with similar characteristics, the hippocampus was extracted to perform electrophysiological studies. Symbiotic-supplemented rats showed a significantly better memory, butyrate concentrations, and neurogenesis. This group also presented an increased firing frequency in hippocampal neurons [and a larger N-methyl-d-aspartate (NMDA)/α-amino-3-hydroxyl-5-methyl-4-isoxazole-propionate (AMPA) current ratio] suggesting an increase in NMDA receptors, which in turn is associated with an enhancement in long-term potentiation and synaptic plasticity. Therefore, our results suggest that symbiotics could restore obesity-related memory impairment and promote synaptic plasticity.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
共生补充(粪肠杆菌和龙舌兰菊素)改善肥胖大鼠的空间记忆和增加海马的可塑性:一项概念验证研究。
肥胖通过全身性低度炎症与认知障碍有关。高脂高糖饮食(HFSDs)也会通过诱导toll样受体4反应或引起生态失调而诱发全身性炎症。本研究旨在评价共生剂补充对三氟sd大鼠空间记忆和工作记忆、丁酸盐浓度、神经发生和电生理恢复的影响。第一个实验,Sprague-Dawley雄性大鼠给予HFSD治疗10周后,随机分为2组(每组n = 10):水(对照)或屎肠球菌+菊粉(共生)治疗5周。第5周分别采用Morris水迷宫(MWM)和八臂径向迷宫(RAM)测试分析空间记忆和工作记忆,两项测试间隔1周。在研究结束时,测定粪便和海马神经发生的丁酸盐水平。在第二个具有类似特征的实验中,提取海马体进行电生理研究。共生补充的大鼠表现出明显更好的记忆、丁酸盐浓度和神经发生。这组海马神经元的放电频率也增加了[并且n -甲基-d-天冬氨酸(NMDA)/α-氨基-3-羟基-5-甲基-4-异恶唑-丙酸(AMPA)电流比更大],表明NMDA受体增加,这反过来又与长期增强和突触可塑性增强有关。因此,我们的研究结果表明,共生物质可以恢复肥胖相关的记忆障碍,并促进突触可塑性。
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 去求助
来源期刊
Cell Transplantation
Cell Transplantation 生物-细胞与组织工程
CiteScore
6.00
自引率
3.00%
发文量
97
审稿时长
6 months
期刊介绍: Cell Transplantation, The Regenerative Medicine Journal is an open access, peer reviewed journal that is published 12 times annually. Cell Transplantation is a multi-disciplinary forum for publication of articles on cell transplantation and its applications to human diseases. Articles focus on a myriad of topics including the physiological, medical, pre-clinical, tissue engineering, stem cell, and device-oriented aspects of the nervous, endocrine, cardiovascular, and endothelial systems, as well as genetically engineered cells. Cell Transplantation also reports on relevant technological advances, clinical studies, and regulatory considerations related to the implantation of cells into the body in order to provide complete coverage of the field.
期刊最新文献
ASNTR 2024 Abstracts Role of Hedgehog Signaling Pathways in Multipotent Mesenchymal Stem Cells Differentiation Hematopoietic Stem Cell Transplantation in Sickle Cell Disease: A Multidimentional Review Alpha-1 Antitrypsin Augmentation Therapy in Chronic Pancreatitis Patients Undergoing Total Pancreatectomy and Islet Autotransplantation: A Randomized, Controlled Study Persistent Cytopenia After CD19 CAR T Therapy in Relapsed/Refractory DLBCL Patients Could Be a Predictor of Efficacy and Side Effects
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1