• 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
Autophagy and post-ischemic conditioning in retinal ischemia.自噬与缺血后适应在视网膜缺血中的作用。
Autophagy. 2021 Jun;17(6):1479-1499. doi: 10.1080/15548627.2020.1767371. Epub 2020 May 26.
2
The neurosteroid allopregnanolone protects retinal neurons by effects on autophagy and GABRs/GABA receptors in rat glaucoma models.在大鼠青光眼模型中,神经甾体别孕烯醇酮通过对自噬以及GABRs/γ-氨基丁酸受体的作用来保护视网膜神经元。
Autophagy. 2021 Mar;17(3):743-760. doi: 10.1080/15548627.2020.1731270. Epub 2020 Feb 27.
3
Clearance of damaged mitochondria via mitophagy is important to the protective effect of ischemic preconditioning in kidneys.通过线粒体自噬清除受损的线粒体对于缺血预处理在肾脏中的保护作用很重要。
Autophagy. 2019 Dec;15(12):2142-2162. doi: 10.1080/15548627.2019.1615822. Epub 2019 May 22.
4
Treatments targeting autophagy ameliorate the age-related macular degeneration phenotype in mice lacking APOE (apolipoprotein E).针对自噬的治疗方法改善了缺乏 APOE(载脂蛋白 E)的小鼠的年龄相关性黄斑变性表型。
Autophagy. 2022 Oct;18(10):2368-2384. doi: 10.1080/15548627.2022.2034131. Epub 2022 Feb 23.
5
Ischemia-induced upregulation of autophagy preludes dysfunctional lysosomal storage and associated synaptic impairments in neurons.缺血诱导的自噬上调先于神经元中功能失调的溶酶体储存和相关的突触损伤。
Autophagy. 2021 Jun;17(6):1519-1542. doi: 10.1080/15548627.2020.1840796. Epub 2020 Nov 12.
6
BNIP3L-mediated mitophagy is required for mitochondrial remodeling during the differentiation of optic nerve oligodendrocytes.BNIP3L 介导的线粒体自噬是视神经少突胶质细胞分化过程中线粒体重塑所必需的。
Autophagy. 2021 Oct;17(10):3140-3159. doi: 10.1080/15548627.2020.1871204. Epub 2021 Jan 19.
7
Autophagy is involved in the neuroprotective effect of nicotiflorin.自噬参与了山奈酚的神经保护作用。
J Ethnopharmacol. 2021 Oct 5;278:114279. doi: 10.1016/j.jep.2021.114279. Epub 2021 Jun 1.
8
Metformin alleviates hyperglycemia-induced endothelial impairment by downregulating autophagy via the Hedgehog pathway.二甲双胍通过 Hedgehog 通路下调自噬来缓解高血糖引起的内皮损伤。
Autophagy. 2019 May;15(5):843-870. doi: 10.1080/15548627.2019.1569913. Epub 2019 Jan 27.
9
Autophagy was activated in injured astrocytes and mildly decreased cell survival following glucose and oxygen deprivation and focal cerebral ischemia.在葡萄糖和氧剥夺以及局灶性脑缺血后,损伤的星形胶质细胞中自噬被激活,细胞存活能力轻度下降。
Autophagy. 2010 Aug;6(6):738-53. doi: 10.4161/auto.6.6.12573. Epub 2010 Aug 3.
10
Increased LCN2 (lipocalin 2) in the RPE decreases autophagy and activates inflammasome-ferroptosis processes in a mouse model of dry AMD.在干性 AMD 小鼠模型中,RPE 中 LCN2(脂联素 2)的增加会减少自噬并激活炎症小体-铁死亡过程。
Autophagy. 2023 Jan;19(1):92-111. doi: 10.1080/15548627.2022.2062887. Epub 2022 Apr 26.

引用本文的文献

1
Upregulation of SQSTM1 Regulates Ferroptosis and Oxidative Stress in Müller Cells of the Diabetic Neural Retina by Modulating ACSL4.SQSTM1的上调通过调节ACSL4来调控糖尿病神经视网膜Müller细胞中的铁死亡和氧化应激。
J Diabetes Res. 2025 Aug 13;2025:1924668. doi: 10.1155/jdr/1924668. eCollection 2025.
2
Brosimine B and the biphasic dose-response: insights into hormesis and retinal neuroprotection.溴西明B与双相剂量反应:对兴奋效应和视网膜神经保护的见解
Front Pharmacol. 2025 Apr 8;16:1558726. doi: 10.3389/fphar.2025.1558726. eCollection 2025.
3
Autophagy: a double-edged sword in ischemia-reperfusion injury.自噬:缺血再灌注损伤中的双刃剑
Cell Mol Biol Lett. 2025 Apr 7;30(1):42. doi: 10.1186/s11658-025-00713-x.
4
Idebenone Protects Photoreceptors Impaired by Oxidative Phosphorylation Disorder in Retinal Detachment.艾地苯醌可保护因视网膜脱离中氧化磷酸化障碍而受损的光感受器。
Invest Ophthalmol Vis Sci. 2025 Jan 2;66(1):17. doi: 10.1167/iovs.66.1.17.
5
Quercetin activates autophagy in the distal ischemic area of random skin flaps through Beclin1 to enhance the adaptability to energy deficiency.槲皮素通过Beclin1激活随意皮瓣远端缺血区域的自噬,以增强对能量缺乏的适应性。
Heliyon. 2024 Sep 29;10(20):e38181. doi: 10.1016/j.heliyon.2024.e38181. eCollection 2024 Oct 30.
6
Optimization of an Ischemic Retinopathy Mouse Model and the Consequences of Hypoxia in a Time-Dependent Manner.缺血性视网膜病变小鼠模型的优化及其在时间依赖性缺氧中的后果。
Int J Mol Sci. 2024 Jul 23;25(15):8008. doi: 10.3390/ijms25158008.
7
The role of glucagon-like peptide-1/GLP-1R and autophagy in diabetic cardiovascular disease.胰高血糖素样肽-1/胰高血糖素样肽-1受体(GLP-1/GLP-1R)与自噬在糖尿病性心血管疾病中的作用
Pharmacol Rep. 2024 Aug;76(4):754-779. doi: 10.1007/s43440-024-00609-1. Epub 2024 Jun 19.
8
The potential mechanism and clinical application value of remote ischemic conditioning in stroke.远程缺血预处理在脑卒中中的潜在机制及临床应用价值
Neural Regen Res. 2025 Jun 1;20(6):1613-1627. doi: 10.4103/NRR.NRR-D-23-01800. Epub 2024 Jun 3.
9
Neuroprotective effects of apigenin on retinal ganglion cells in ischemia/reperfusion: modulating mitochondrial dynamics in in vivo and in vitro models.芹菜素对缺血/再灌注视网膜神经节细胞的神经保护作用:在体内和体外模型中调节线粒体动力学。
J Transl Med. 2024 May 13;22(1):447. doi: 10.1186/s12967-024-05260-1.
10
Resilience to diabetic retinopathy.糖尿病视网膜病变的抵抗力。
Prog Retin Eye Res. 2024 Jul;101:101271. doi: 10.1016/j.preteyeres.2024.101271. Epub 2024 May 11.

本文引用的文献

1
Müller Cells Stabilize Microvasculature through Hypoxic Preconditioning.米勒细胞通过缺氧预处理稳定微血管系统。
Cell Physiol Biochem. 2019;52(4):668-680. doi: 10.33594/000000047.
2
Mesenchymal stem cell-derived extracellular vesicles and retinal ischemia-reperfusion.间质干细胞衍生的细胞外囊泡与视网膜缺血再灌注。
Biomaterials. 2019 Mar;197:146-160. doi: 10.1016/j.biomaterials.2019.01.016. Epub 2019 Jan 9.
3
Aged kidney: can we protect it? Autophagy, mitochondria and mechanisms of ischemic preconditioning.老年肾脏:我们能保护它吗?自噬、线粒体和缺血预处理机制。
Cell Cycle. 2018;17(11):1291-1309. doi: 10.1080/15384101.2018.1482149. Epub 2018 Jul 25.
4
Inhibiting autophagy reduces retinal degeneration caused by protein misfolding.抑制自噬可减少由蛋白质错误折叠引起的视网膜变性。
Autophagy. 2018;14(7):1226-1238. doi: 10.1080/15548627.2018.1463121. Epub 2018 Jul 13.
5
Haemodilution and head-down tilting induce functional injury in the rat optic nerve: A model for peri-operative ischemic optic neuropathy.血液稀释和头低位倾斜导致大鼠视神经功能损伤:一种围手术期缺血性视神经病变模型。
Eur J Anaesthesiol. 2018 Nov;35(11):840-847. doi: 10.1097/EJA.0000000000000829.
6
Gene expression in retinal ischemic post-conditioning.视网膜缺血后处理中的基因表达。
Graefes Arch Clin Exp Ophthalmol. 2018 May;256(5):935-949. doi: 10.1007/s00417-018-3905-0. Epub 2018 Mar 5.
7
Neuroprotective strategies for retinal disease.神经保护策略治疗视网膜疾病。
Prog Retin Eye Res. 2018 Jul;65:50-76. doi: 10.1016/j.preteyeres.2018.02.002. Epub 2018 Feb 23.
8
Oxidation of Atg3 and Atg7 mediates inhibition of autophagy.Atg3和Atg7的氧化介导自噬抑制。
Nat Commun. 2018 Jan 8;9(1):95. doi: 10.1038/s41467-017-02352-z.
9
Axonal Protection by Ripasudil, a Rho Kinase Inhibitor, via Modulating Autophagy in TNF-Induced Optic Nerve Degeneration.Rho激酶抑制剂ripasudil通过调节自噬对肿瘤坏死因子诱导的视神经变性发挥轴突保护作用。
Invest Ophthalmol Vis Sci. 2017 Oct 1;58(12):5056-5064. doi: 10.1167/iovs.17-22000.
10
Click Chemistry for Analysis of Cell Proliferation in Flow Cytometry.用于流式细胞术中细胞增殖分析的点击化学
Curr Protoc Cytom. 2017 Oct 2;82:7.49.1-7.49.30. doi: 10.1002/cpcy.24.

自噬与缺血后适应在视网膜缺血中的作用。

Autophagy and post-ischemic conditioning in retinal ischemia.

机构信息

Department of Anesthesiology, And College of Medicine, University of Illinois at Chicago, Chicago, IL, USA.

Department of Chemistry, College of Liberal Arts and Sciences, University of Illinois at Chicago, Chicago, IL, USA.

出版信息

Autophagy. 2021 Jun;17(6):1479-1499. doi: 10.1080/15548627.2020.1767371. Epub 2020 May 26.

DOI:10.1080/15548627.2020.1767371
PMID:32452260
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8205079/
Abstract

Retinal ischemia is a major cause of vision loss and a common underlying mechanism associated with diseases, such as diabetic retinopathy and central retinal artery occlusion. We have previously demonstrated the robust neuroprotection in retina induced by post-conditioning (post-C), a brief period of ischemia, 24 h, following a prolonged and damaging initial ischemia. The mechanisms underlying post-C-mediated retinal protection are largely uncharacterized. We hypothesized that macroautophagy/autophagy is a mediator of post-C-induced neuroprotection. This study employed an model of oxygen glucose deprivation (OGD) in the retinal R28 neuronal cell line, and an rat model of retinal ischemic injury. , there were significant increases in autophagy proteins, MAP1LC3-II/LC3-II, and decreases in SQSTM1/p62 (sequestosome 1) in ischemia/post-C . ischemia/sham post-C. Blockade of and decreased LC3-II, increased SQSTM1, attenuated the functional protective effect of post-C, and increased histological damage and TUNEL compared to non-silencing siRNA. TUNEL after ischemia was found in retinal ganglion, amacrine, and photoreceptor cells. Blockade of attenuated the post-C neuroprotection by a brief period of OGD . Moreover, , post-C attenuated cell death, loss of cellular proliferation, and defective autophagic flux from prolonged OGD. Stimulating autophagy using Tat-Beclin 1 rescued retinal neurons from cell death after OGD. As a whole, our results suggest that autophagy is required for the neuroprotective effect of retinal ischemic post-conditioning and augmentation of autophagy offers promise in the treatment of retinal ischemic injury.: BECN1: Beclin 1, autophagy related; DAPI: 4',6-diamidino-2-phenylindole; DR: diabetic retinopathy; EdU: 5-ethynyl-2'-deoxyuridine; ERG: Electroretinogram; FITC: Fluorescein isothiocyanate; GCL: Ganglion cell layer; GFAP: Glial fibrillary acidic protein; INL: Inner nuclear layer; IPL: Inner plexiform layer; MAP1LC3/LC3: Microtubule-associated protein 1 light chain 3; OGD: Oxygen-glucose deprivation; ONL: Outer nuclear layer; OP: Oscillatory potential; PFA: Paraformaldehyde; PL: Photoreceptor layer; post-C: post-conditioning; RFP: Red fluorescent protein; RGC: Retinal ganglion cell; RPE: Retinal pigment epithelium; RT-PCR: Real-time polymerase chain reaction; SEM: Standard error of the mean; siRNA: Small interfering RNA; SQSTM1: Sequestosome 1; STR: Scotopic threshold response; Tat: Trans-activator of transcription; TUNEL: Terminal deoxynucleotidyl transferase dUTP nick end labeling.

摘要

视网膜缺血是视力丧失的主要原因,也是与糖尿病视网膜病变和中央视网膜动脉阻塞等疾病相关的常见潜在机制。我们之前已经证明了后处理(post-C)在诱导视网膜中强大的神经保护作用,即短暂的缺血期,在长时间和损伤性初始缺血后 24 小时。后处理介导的视网膜保护的机制在很大程度上尚未确定。我们假设巨自噬/自噬是 post-C 诱导的神经保护的介质。本研究采用视网膜 R28 神经元细胞系的氧葡萄糖剥夺(OGD)模型和大鼠视网膜缺血性损伤模型。结果发现,在缺血/后-C 中,自噬蛋白 MAP1LC3-II/LC3-II 显著增加,而 SQSTM1/p62(自噬体 1)减少。与假缺血/后-C 相比,缺血/Sham 后-C 中的自噬标志物 LC3-II 减少,而 SQSTM1 增加。与非沉默 siRNA 相比,后-C 的功能保护作用减弱,组织学损伤和 TUNEL 增加。在视网膜神经节细胞、无长突细胞和光感受器细胞中发现了 TUNEL 后缺血。Beclin 1 的短暂 OGD 抑制了后-C 的神经保护作用。此外,后-C 减轻了长期 OGD 引起的细胞死亡、细胞增殖丧失和缺陷自噬流。用 Tat-Beclin 1 刺激自噬可挽救 OGD 后视网膜神经元的死亡。总的来说,我们的结果表明自噬是视网膜缺血后处理的神经保护作用所必需的,并且增强自噬为治疗视网膜缺血性损伤提供了希望。