Targeting MAPK14 in microglial cells: neuroimmune implications of Panax ginseng in post-stroke inflammation.

IF 2.8 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Hongxu Guan, Xiaoting Yang, Mingfeng Yang, Haitao Wang
{"title":"Targeting MAPK14 in microglial cells: neuroimmune implications of Panax ginseng in post-stroke inflammation.","authors":"Hongxu Guan, Xiaoting Yang, Mingfeng Yang, Haitao Wang","doi":"10.1093/jpp/rgae067","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>This study investigates the molecular mechanisms through which Panax ginseng and Panax notoginseng saponin (PNS) mitigate neuroinflammatory damage and promote neural repair postischemic stroke, utilizing bioinformatics, and experimental approaches.</p><p><strong>Background: </strong>Cerebral infarction significantly contributes to disability worldwide, with chronic neuroinflammation worsening cognitive impairments and leading to neurodegenerative diseases. Addressing neuroimmune interactions is crucial for slowing disease progression and enhancing patient recovery, highlighting the need for advanced research in neuroimmune regulatory mechanisms and therapeutic strategies.</p><p><strong>Objective: </strong>To elucidate the effects of the traditional Chinese medicine components Panax ginseng and PNS on neuroinflammatory damage following ischemic stroke, focusing on the molecular pathways involved in mitigating inflammation and facilitating neural repair.</p><p><strong>Methods: </strong>The study employs single-cell sequencing and transcriptomic analysis to investigate gene expression changes associated with cerebral infarction. Gene set enrichment analysis and weighted gene co-expression network analysis are used to identify key molecular markers and core genes. Furthermore, pharmacological profiling, including functional assays, assesses the impact of Ginsenoside-Rc, a PNS derivative, on microglial cell viability, cytokine production, and reactive oxygen species (ROS) levels.</p><p><strong>Results: </strong>Our analysis revealed that MAPK14 is a critical mediator in the neuroinflammatory response to ischemic stroke. Ginsenoside-Rc potentially targets and modulates MAPK14 activity to suppress inflammation. Experimental validation showed that Ginsenoside-Rc treatment, combined with MAPK14 silencing, significantly alters MAPK14 expression and mitigates neuroinflammatory damage, evidenced by reduced microglial cell death, inflammatory factor secretion, and ROS production.</p><p><strong>Conclusion: </strong>Ginsenoside-Rc's modulation of MAPK14 offers a promising therapeutic strategy for reducing neuroinflammation and potentially improving cognitive recovery post-ischemic stroke. This supports the therapeutic application of the traditional Chinese medicine Sanqi in ischemic stroke care, providing a theoretical and experimental foundation for its use.</p><p><strong>Others: </strong>Future work will focus on extending these findings through clinical trials to evaluate the efficacy and safety of Ginsenoside-Rc in human subjects, aiming to translate these promising preclinical results into practical therapeutic interventions for ischemic stroke recovery.</p>","PeriodicalId":16960,"journal":{"name":"Journal of Pharmacy and Pharmacology","volume":null,"pages":null},"PeriodicalIF":2.8000,"publicationDate":"2024-06-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Pharmacy and Pharmacology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/jpp/rgae067","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
引用次数: 0

Abstract

Aim: This study investigates the molecular mechanisms through which Panax ginseng and Panax notoginseng saponin (PNS) mitigate neuroinflammatory damage and promote neural repair postischemic stroke, utilizing bioinformatics, and experimental approaches.

Background: Cerebral infarction significantly contributes to disability worldwide, with chronic neuroinflammation worsening cognitive impairments and leading to neurodegenerative diseases. Addressing neuroimmune interactions is crucial for slowing disease progression and enhancing patient recovery, highlighting the need for advanced research in neuroimmune regulatory mechanisms and therapeutic strategies.

Objective: To elucidate the effects of the traditional Chinese medicine components Panax ginseng and PNS on neuroinflammatory damage following ischemic stroke, focusing on the molecular pathways involved in mitigating inflammation and facilitating neural repair.

Methods: The study employs single-cell sequencing and transcriptomic analysis to investigate gene expression changes associated with cerebral infarction. Gene set enrichment analysis and weighted gene co-expression network analysis are used to identify key molecular markers and core genes. Furthermore, pharmacological profiling, including functional assays, assesses the impact of Ginsenoside-Rc, a PNS derivative, on microglial cell viability, cytokine production, and reactive oxygen species (ROS) levels.

Results: Our analysis revealed that MAPK14 is a critical mediator in the neuroinflammatory response to ischemic stroke. Ginsenoside-Rc potentially targets and modulates MAPK14 activity to suppress inflammation. Experimental validation showed that Ginsenoside-Rc treatment, combined with MAPK14 silencing, significantly alters MAPK14 expression and mitigates neuroinflammatory damage, evidenced by reduced microglial cell death, inflammatory factor secretion, and ROS production.

Conclusion: Ginsenoside-Rc's modulation of MAPK14 offers a promising therapeutic strategy for reducing neuroinflammation and potentially improving cognitive recovery post-ischemic stroke. This supports the therapeutic application of the traditional Chinese medicine Sanqi in ischemic stroke care, providing a theoretical and experimental foundation for its use.

Others: Future work will focus on extending these findings through clinical trials to evaluate the efficacy and safety of Ginsenoside-Rc in human subjects, aiming to translate these promising preclinical results into practical therapeutic interventions for ischemic stroke recovery.

靶向小胶质细胞中的 MAPK14:三七对中风后炎症的神经免疫影响
目的:本研究利用生物信息学和实验方法,探讨三七和三七皂苷(PNS)减轻神经炎症损伤和促进缺血性中风后神经修复的分子机制:背景:脑梗塞是导致全球残疾的重要原因,慢性神经炎症会加重认知障碍并导致神经退行性疾病。解决神经免疫相互作用问题对于延缓疾病进展和促进患者康复至关重要,因此需要对神经免疫调节机制和治疗策略进行深入研究:目的:阐明中药成分三七和 PNS 对缺血性脑卒中后神经炎症损伤的影响,重点研究减轻炎症和促进神经修复的分子通路:本研究采用单细胞测序和转录组分析方法研究与脑梗死相关的基因表达变化。基因组富集分析和加权基因共表达网络分析用于确定关键分子标记和核心基因。此外,包括功能测定在内的药理分析评估了人参皂苷-Rc(一种 PNS 衍生物)对小胶质细胞活力、细胞因子产生和活性氧(ROS)水平的影响:结果:我们的分析表明,MAPK14 是缺血性中风神经炎症反应的关键介质。人参皂苷-Rc可靶向调节MAPK14的活性,从而抑制炎症反应。实验验证表明,人参皂苷-Rc治疗结合MAPK14沉默,可显著改变MAPK14的表达,减轻神经炎症损伤,表现为减少小胶质细胞死亡、炎症因子分泌和ROS产生:结论:人参皂苷-Rc 对 MAPK14 的调节为减轻神经炎症和改善缺血性中风后的认知恢复提供了一种很有前景的治疗策略。这支持了传统中药三七在缺血性中风治疗中的应用,为其应用提供了理论和实验基础:未来的工作重点是通过临床试验扩展这些研究结果,评估人参皂苷-Rc 在人体中的疗效和安全性,旨在将这些有前景的临床前研究结果转化为缺血性中风康复的实际治疗干预措施。
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
6.60
自引率
0.00%
发文量
91
审稿时长
3 months
期刊介绍: JPP keeps pace with new research on how drug action may be optimized by new technologies, and attention is given to understanding and improving drug interactions in the body. At the same time, the journal maintains its established and well-respected core strengths in areas such as pharmaceutics and drug delivery, experimental and clinical pharmacology, biopharmaceutics and drug disposition, and drugs from natural sources. JPP publishes at least one special issue on a topical theme each year.
×
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