• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

相似文献

1
Lipid-based therapies against SARS-CoV-2 infection.针对 SARS-CoV-2 感染的脂质体疗法。
Rev Med Virol. 2021 Sep;31(5):1-13. doi: 10.1002/rmv.2214. Epub 2021 Jan 13.
2
The roles of lipids in SARS-CoV-2 viral replication and the host immune response.脂质在 SARS-CoV-2 病毒复制和宿主免疫反应中的作用。
J Lipid Res. 2021;62:100129. doi: 10.1016/j.jlr.2021.100129. Epub 2021 Sep 29.
3
Dissecting lipid metabolism alterations in SARS-CoV-2.解析 SARS-CoV-2 中的脂质代谢改变。
Prog Lipid Res. 2021 Apr;82:101092. doi: 10.1016/j.plipres.2021.101092. Epub 2021 Feb 8.
4
Perturbed Lipid Metabolism Transduction Pathways in SARS-CoV-2 Infection and Their Possible Treating Nutraceuticals.严重急性呼吸综合征冠状病毒2(SARS-CoV-2)感染中脂质代谢转导途径的紊乱及其可能的治疗性营养保健品
J Am Nutr Assoc. 2024 Sep-Oct;43(7):614-626. doi: 10.1080/27697061.2024.2359084. Epub 2024 May 28.
5
The SARS-Coronavirus Infection Cycle: A Survey of Viral Membrane Proteins, Their Functional Interactions and Pathogenesis.SARS-CoV 感染周期:病毒膜蛋白、功能相互作用及其发病机制概述。
Int J Mol Sci. 2021 Jan 28;22(3):1308. doi: 10.3390/ijms22031308.
6
The Role of Lipid Metabolism in COVID-19 Virus Infection and as a Drug Target.脂代谢在 COVID-19 病毒感染中的作用及其作为药物靶点的研究。
Int J Mol Sci. 2020 May 17;21(10):3544. doi: 10.3390/ijms21103544.
7
Metabolic alterations upon SARS-CoV-2 infection and potential therapeutic targets against coronavirus infection.新冠病毒感染后的代谢改变和针对冠状病毒感染的潜在治疗靶点。
Signal Transduct Target Ther. 2023 Jun 7;8(1):237. doi: 10.1038/s41392-023-01510-8.
8
Modifications of lipid pathways restrict SARS-CoV-2 propagation in human induced pluripotent stem cell-derived 3D airway organoids.脂质代谢通路的修饰可限制 SARS-CoV-2 在人诱导多能干细胞衍生的 3D 气道类器官中的复制。
J Adv Res. 2024 Jun;60:127-140. doi: 10.1016/j.jare.2023.08.005. Epub 2023 Aug 7.
9
Palmitoylethanolamide (PEA) Inhibits SARS-CoV-2 Entry by Interacting with S Protein and ACE-2 Receptor.棕榈酰乙醇酰胺(PEA)通过与 S 蛋白和 ACE-2 受体相互作用抑制 SARS-CoV-2 进入。
Viruses. 2022 May 17;14(5):1080. doi: 10.3390/v14051080.
10
Cholesterol-Rich Lipid Rafts as Platforms for SARS-CoV-2 Entry.富含胆固醇的脂筏作为 SARS-CoV-2 进入的平台。
Front Immunol. 2021 Dec 16;12:796855. doi: 10.3389/fimmu.2021.796855. eCollection 2021.

引用本文的文献

1
Plasma nontargeted metabolomics study of H1N1 and H3N2 influenza in children.儿童甲型H1N1和H3N2流感的血浆非靶向代谢组学研究
Front Cell Infect Microbiol. 2025 Apr 4;15:1537726. doi: 10.3389/fcimb.2025.1537726. eCollection 2025.
2
Integrated multi-omics analysis reveals liver metabolic reprogramming by fish iridovirus and antiviral function of alpha-linolenic acid.整合多组学分析揭示鱼类虹彩病毒引起的肝脏代谢重编程和α-亚麻酸的抗病毒功能。
Zool Res. 2024 May 18;45(3):520-534. doi: 10.24272/j.issn.2095-8137.2024.028.
3
Untargeted LC-MS metabolomics reveals the metabolic responses in olive flounder subjected to hirame rhabdovirus infection.非靶向 LC-MS 代谢组学揭示了感染牙鲆虹彩病毒的牙鲆的代谢反应。
Front Immunol. 2023 Aug 28;14:1148740. doi: 10.3389/fimmu.2023.1148740. eCollection 2023.
4
Deficiency in the production of antibodies to lipids correlates with increased lipid metabolism in severe COVID-19 patients.严重 COVID-19 患者体内产生针对脂质的抗体不足与脂质代谢增加相关。
Front Immunol. 2023 Jun 23;14:1188786. doi: 10.3389/fimmu.2023.1188786. eCollection 2023.
5
Cyclic lipopeptides as membrane fusion inhibitors against SARS-CoV-2: New tricks for old dogs.环状脂肽作为抗 SARS-CoV-2 的膜融合抑制剂:老把戏新玩法。
Antiviral Res. 2023 Apr;212:105575. doi: 10.1016/j.antiviral.2023.105575. Epub 2023 Mar 2.
6
Network-based drug repurposing for the treatment of COVID-19 patients in different clinical stages.基于网络的药物重利用用于治疗不同临床阶段的COVID-19患者。
Heliyon. 2023 Mar;9(3):e14059. doi: 10.1016/j.heliyon.2023.e14059. Epub 2023 Feb 24.
7
SARS-CoV-2-free residual proteins mediated phenotypic and metabolic changes in peripheral blood monocytic-derived macrophages in support of viral pathogenesis.SARS-CoV-2 无残留蛋白介导外周血单核细胞衍生巨噬细胞的表型和代谢变化,支持病毒发病机制。
PLoS One. 2023 Jan 19;18(1):e0280592. doi: 10.1371/journal.pone.0280592. eCollection 2023.
8
A Review of the Multi-Systemic Complications of a Ketogenic Diet in Children and Infants with Epilepsy.儿童和婴儿癫痫生酮饮食的多系统并发症综述
Children (Basel). 2022 Sep 10;9(9):1372. doi: 10.3390/children9091372.
9
Obesity and COVID-19: What are the Consequences?肥胖与 COVID-19:后果如何?
Horm Metab Res. 2022 Aug;54(8):496-502. doi: 10.1055/a-1878-9757. Epub 2022 Jun 20.
10
Small-molecule metabolome identifies potential therapeutic targets against COVID-19.小分子代谢组学鉴定出针对 COVID-19 的潜在治疗靶点。
Sci Rep. 2022 Jun 15;12(1):10029. doi: 10.1038/s41598-022-14050-y.

本文引用的文献

1
Inhibitors of VPS34 and fatty-acid metabolism suppress SARS-CoV-2 replication.VPS34 和脂肪酸代谢抑制剂抑制 SARS-CoV-2 复制。
Cell Rep. 2021 Aug 3;36(5):109479. doi: 10.1016/j.celrep.2021.109479. Epub 2021 Jul 20.
2
Elovanoids downregulate SARS-CoV-2 cell-entry, canonical mediators and enhance protective signaling in human alveolar cells.Elovanoids 下调 SARS-CoV-2 细胞进入、经典介质并增强人肺泡细胞的保护信号。
Sci Rep. 2021 Jun 10;11(1):12324. doi: 10.1038/s41598-021-91794-z.
3
A metabolic modeling approach reveals promising therapeutic targets and antiviral drugs to combat COVID-19.一种代谢建模方法揭示了对抗新冠病毒有前景的治疗靶点和抗病毒药物。
Sci Rep. 2021 Jun 7;11(1):11982. doi: 10.1038/s41598-021-91526-3.
4
Lipid droplets fuel SARS-CoV-2 replication and production of inflammatory mediators.脂滴为 SARS-CoV-2 的复制和炎症介质的产生提供燃料。
PLoS Pathog. 2020 Dec 16;16(12):e1009127. doi: 10.1371/journal.ppat.1009127. eCollection 2020 Dec.
5
HDL-scavenger receptor B type 1 facilitates SARS-CoV-2 entry.HDL scavenger receptor B type 1 促进了 SARS-CoV-2 的进入。
Nat Metab. 2020 Dec;2(12):1391-1400. doi: 10.1038/s42255-020-00324-0. Epub 2020 Nov 26.
6
Pharmacological Inhibition of Acid Sphingomyelinase Prevents Uptake of SARS-CoV-2 by Epithelial Cells.酸鞘磷脂酶的药理学抑制可防止 SARS-CoV-2 被上皮细胞摄取。
Cell Rep Med. 2020 Nov 17;1(8):100142. doi: 10.1016/j.xcrm.2020.100142. Epub 2020 Oct 29.
7
ssRNA Virus and Host Lipid Rearrangements: Is There a Role for Lipid Droplets in SARS-CoV-2 Infection?单链RNA病毒与宿主脂质重排:脂滴在新型冠状病毒感染中起作用吗?
Front Mol Biosci. 2020 Oct 8;7:578964. doi: 10.3389/fmolb.2020.578964. eCollection 2020.
8
Membrane heist: Coronavirus host membrane remodeling during replication.膜掠夺:冠状病毒在复制过程中对宿主膜的重塑。
Biochimie. 2020 Dec;179:229-236. doi: 10.1016/j.biochi.2020.10.010. Epub 2020 Oct 25.
9
Bioactive Lipids in COVID-19-Further Evidence.COVID-19 相关生物活性脂质:更多证据。
Arch Med Res. 2021 Jan;52(1):107-120. doi: 10.1016/j.arcmed.2020.09.006. Epub 2020 Sep 9.
10
Free fatty acid binding pocket in the locked structure of SARS-CoV-2 spike protein.新冠病毒 Spike 蛋白锁闭结构中的游离脂肪酸结合口袋。
Science. 2020 Nov 6;370(6517):725-730. doi: 10.1126/science.abd3255. Epub 2020 Sep 21.

针对 SARS-CoV-2 感染的脂质体疗法。

Lipid-based therapies against SARS-CoV-2 infection.

机构信息

Department of Applied Biology, College of Sciences, University of Sharjah, Sharjah, United Arab Emirates.

Research Institute for Medical and Health Sciences, University of Sharjah, Sharjah, United Arab Emirates.

出版信息

Rev Med Virol. 2021 Sep;31(5):1-13. doi: 10.1002/rmv.2214. Epub 2021 Jan 13.

DOI:10.1002/rmv.2214
PMID:34546604
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8013851/
Abstract

Viruses have evolved to manipulate host lipid metabolism to benefit their replication cycle. Enveloped viruses, including coronaviruses, use host lipids in various stages of the viral life cycle, particularly in the formation of replication compartments and envelopes. Host lipids are utilised by the virus in receptor binding, viral fusion and entry, as well as viral replication. Association of dyslipidaemia with the pathological development of Covid-19 raises the possibility that exploitation of host lipid metabolism might have therapeutic benefit against severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). In this review, promising host lipid targets are discussed along with potential inhibitors. In addition, specific host lipids are involved in the inflammatory responses due to viral infection, so lipid supplementation represents another potential strategy to counteract the severity of viral infection. Furthermore, switching the lipid metabolism through a ketogenic diet is another potential way of limiting the effects of viral infection. Taken together, restricting the access of host lipids to the virus, either by using lipid inhibitors or supplementation with exogenous lipids, might significantly limit SARS-CoV-2 infection and/or severity.

摘要

病毒已经进化到可以操纵宿主的脂质代谢来促进其复制周期。包膜病毒,包括冠状病毒,在病毒生命周期的各个阶段利用宿主脂质,特别是在复制隔间和包膜的形成中。宿主脂质在病毒的受体结合、病毒融合和进入以及病毒复制中被病毒利用。血脂异常与 COVID-19 的病理发展之间的关联提出了这样一种可能性,即利用宿主脂质代谢可能对抗严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2)具有治疗益处。在这篇综述中,讨论了有前途的宿主脂质靶点以及潜在的抑制剂。此外,由于病毒感染,特定的宿主脂质参与炎症反应,因此脂质补充代表了另一种对抗病毒感染严重程度的潜在策略。此外,通过生酮饮食改变脂质代谢也是限制病毒感染影响的另一种潜在方法。综上所述,通过使用脂质抑制剂或补充外源性脂质来限制宿主脂质进入病毒,可能会显著限制 SARS-CoV-2 的感染和/或严重程度。