High fat diet and low dose-rotenone exposure exacerbate Parkinson's disease like pathology through gut-brain axis disruption

IF 4.2 2区 医学 Q1 NEUROSCIENCES
Aditya A. Singh , Zarna Pathak , Ashwini Chawathe , Manjeet Chopra , Vimal P. Rupareliya , Nitish Sharma , Hemant Kumar
{"title":"High fat diet and low dose-rotenone exposure exacerbate Parkinson's disease like pathology through gut-brain axis disruption","authors":"Aditya A. Singh ,&nbsp;Zarna Pathak ,&nbsp;Ashwini Chawathe ,&nbsp;Manjeet Chopra ,&nbsp;Vimal P. Rupareliya ,&nbsp;Nitish Sharma ,&nbsp;Hemant Kumar","doi":"10.1016/j.expneurol.2025.115384","DOIUrl":null,"url":null,"abstract":"<div><div>Parkinson's disease (PD) affects millions worldwide. In recent years, the role of the gut-brain axis and gut microbiome alterations in neurodegenerative diseases has gained significant attention. Lifestyle and environment factors play a crucial role in shaping the overall health. Herein, we investigated whether obesity induced by high-fat diet (HFD) combined with low-dose rotenone (5 mg/kg; orally, twice a day) exacerbates PD-like pathology. Our findings reveal non-motor symptoms of PD alongside gut inflammation, α-synuclein (α-syn) accumulation, and dysbiosis, possibly mediated by transient receptor potential vanilloid 1 (TRPV1) channel. In the brain, we observed the characteristic α-syn pathology in the substantia nigra (SN) and the striatum. Finally, we observe neuroinflammation including astrogliosis, microgliosis and increased expression of TRPV1 channel in the SN and striatum possibly hinting to PD like pathological features. The <em>in-vitro</em> findings in N2a and C6 glial cell lines hint towards possible co-relation of increased TRPV1 in response to lipotoxicity and rotenone exposure which was recovered when treated with TRPV1 antagonist; Capsazepine. In summary, we propose that HFD along with low dose rotenone poses a risk for neuronal health; exaggerating the neuroinflammatory states.</div></div>","PeriodicalId":12246,"journal":{"name":"Experimental Neurology","volume":"393 ","pages":"Article 115384"},"PeriodicalIF":4.2000,"publicationDate":"2025-07-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Experimental Neurology","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0014488625002481","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
引用次数: 0

Abstract

Parkinson's disease (PD) affects millions worldwide. In recent years, the role of the gut-brain axis and gut microbiome alterations in neurodegenerative diseases has gained significant attention. Lifestyle and environment factors play a crucial role in shaping the overall health. Herein, we investigated whether obesity induced by high-fat diet (HFD) combined with low-dose rotenone (5 mg/kg; orally, twice a day) exacerbates PD-like pathology. Our findings reveal non-motor symptoms of PD alongside gut inflammation, α-synuclein (α-syn) accumulation, and dysbiosis, possibly mediated by transient receptor potential vanilloid 1 (TRPV1) channel. In the brain, we observed the characteristic α-syn pathology in the substantia nigra (SN) and the striatum. Finally, we observe neuroinflammation including astrogliosis, microgliosis and increased expression of TRPV1 channel in the SN and striatum possibly hinting to PD like pathological features. The in-vitro findings in N2a and C6 glial cell lines hint towards possible co-relation of increased TRPV1 in response to lipotoxicity and rotenone exposure which was recovered when treated with TRPV1 antagonist; Capsazepine. In summary, we propose that HFD along with low dose rotenone poses a risk for neuronal health; exaggerating the neuroinflammatory states.
高脂肪饮食和低剂量鱼藤酮暴露通过肠-脑轴破坏加剧帕金森病的病理。
帕金森病(PD)影响着全世界数百万人。近年来,肠脑轴和肠道微生物组改变在神经退行性疾病中的作用得到了极大的关注。生活方式和环境因素在塑造整体健康方面起着至关重要的作用。在此,我们研究了高脂肪饮食(HFD)联合低剂量鱼藤酮(5 mg/kg;口服,一天两次)加重了pd样病理。我们的研究结果表明,PD的非运动症状伴随着肠道炎症、α-突触核蛋白(α-syn)积累和生态失调,可能是由瞬时受体电位香草样蛋白1 (TRPV1)通道介导的。在大脑中,我们在黑质(SN)和纹状体中观察到特征性的α-syn病理。最后,我们观察到神经炎症包括星形胶质细胞增生、小胶质细胞增生以及SN和纹状体中TRPV1通道的表达增加,可能提示PD样病理特征。N2a和C6胶质细胞系的体外研究结果提示,TRPV1的增加可能与脂肪毒性和鱼藤酮暴露有关,而TRPV1拮抗剂治疗后TRPV1恢复;Capsazepine。总之,我们认为HFD和低剂量鱼藤酮对神经元健康构成风险;夸大了神经炎症状态。
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
Experimental Neurology
Experimental Neurology 医学-神经科学
CiteScore
10.10
自引率
3.80%
发文量
258
审稿时长
42 days
期刊介绍: Experimental Neurology, a Journal of Neuroscience Research, publishes original research in neuroscience with a particular emphasis on novel findings in neural development, regeneration, plasticity and transplantation. The journal has focused on research concerning basic mechanisms underlying neurological 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:604180095
Book学术官方微信