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。

IF 3.2 4区 医学 Q3 CELL & TISSUE ENGINEERING
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
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引用次数: 1

摘要

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

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.

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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.
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