• 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

使用可生物降解微球诱导眼压升高治疗慢性青光眼。六个月随访

Chronic Glaucoma Using Biodegradable Microspheres to Induce Intraocular Pressure Elevation. Six-Month Follow-Up.

作者信息

Rodrigo Maria Jesus, Garcia-Herranz David, Subias Manuel, Martinez-Rincón Teresa, Mendez-Martínez Silvia, Bravo-Osuna Irene, Carretero Ana, Ruberte Jesús, Garcia-Feijoo Julián, Pablo Luis Emilio, Herrero-Vanrell Rocío, Garcia-Martin Elena

机构信息

Miguel Servet Ophthalmology Research Group (GIMSO), Aragon Health Research Institute (IIS Aragon), University of Zaragoza, 50009 Zaragoza, Spain.

National Ocular Pathology Network (OFTARED), Carlos III Health Institute, 28040 Madrid, Spain.

出版信息

Biomedicines. 2021 Jun 16;9(6):682. doi: 10.3390/biomedicines9060682.

DOI:10.3390/biomedicines9060682
PMID:34208744
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8235213/
Abstract

BACKGROUND

To compare two prolonged animal models of glaucoma over 24 weeks of follow-up. A novel pre-trabecular model of chronic glaucoma was achieved by injection of biodegradable poly lactic-co-glycolic acid (PLGA) microspheres (10-20 µm) (Ms20/10) into the ocular anterior chamber to progressively increase ocular hypertension (OHT).

METHODS

Rat right eyes were injected to induce OHT: 50% received a suspension of Ms20/10 in the anterior chamber at 0, 2, 4, 8, 12, 16 and 20 weeks, and the other 50% received a sclerosing episcleral vein injection biweekly (EPIm). Ophthalmological clinical signs, intraocular pressure (IOP), neuroretinal functionality measured by electroretinography (ERG), and structural analysis of the retina, retinal nerve fiber layer (RNFL) and ganglion cell layer (GCL) protocols using optical coherence tomography (OCT) and histological exams were performed.

RESULTS

Both models showed progressive neuroretinal degeneration ( < 0.05), and contralateral eye affectation. The Ms20/10 model showed a more progressive increase in IOP and better preservation of ocular surface. Although no statistical differences were found between models, the EPIm showed a tendency to produce thicker retinal and thinner GCL thicknesses, slower latency and smaller amplitude as measured using ERG, and more aggressive disturbances in retinal histology. In both models, while the GCL showed the greatest percentage loss of thickness, the RNFL showed the greatest and earliest rate of thickness loss.

CONCLUSIONS

The intracameral model with biodegradable microspheres resulted more like the conditions observed in humans. It was obtained by a less-aggressive mechanism, which allows for adequate study of the pathology over longer periods.

摘要

背景

为比较两种在24周随访期内的长期青光眼动物模型。通过将可生物降解的聚乳酸-乙醇酸共聚物(PLGA)微球(10 - 20微米)(Ms20/10)注入眼前房以逐渐升高眼压(OHT),建立了一种新型的小梁前慢性青光眼模型。

方法

对大鼠右眼进行注射以诱导OHT:50%的大鼠在第0、2、4、8、12、16和20周时接受前房内Ms20/10悬浮液注射,另外50%的大鼠每两周接受一次巩膜静脉硬化注射(EPIm)。进行眼科临床体征、眼压(IOP)、通过视网膜电图(ERG)测量的神经视网膜功能,以及使用光学相干断层扫描(OCT)和组织学检查对视网膜、视网膜神经纤维层(RNFL)和神经节细胞层(GCL)进行结构分析。

结果

两种模型均显示出进行性神经视网膜变性(<0.05)以及对侧眼受累。Ms20/10模型显示眼压有更渐进性的升高以及眼表有更好的保存。尽管在模型之间未发现统计学差异,但EPIm显示出视网膜更厚、GCL厚度更薄的趋势,使用ERG测量时潜伏期更长、振幅更小,并且在视网膜组织学上有更严重的干扰。在两种模型中,虽然GCL显示出厚度损失的百分比最大,但RNFL显示出厚度损失的速率最大且最早。

结论

使用可生物降解微球的前房内模型更类似于在人类中观察到的情况。它是通过一种侵袭性较小的机制获得的,这使得能够在更长时间内对病理学进行充分研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/902bfce43e7c/biomedicines-09-00682-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/cce28b27a7e9/biomedicines-09-00682-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/ce84a3713704/biomedicines-09-00682-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/59887b47e282/biomedicines-09-00682-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/3eb19c9f11a3/biomedicines-09-00682-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/8a92b9ed3226/biomedicines-09-00682-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/bb2bff19cbf6/biomedicines-09-00682-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/6a628919e6cc/biomedicines-09-00682-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/753ea797030a/biomedicines-09-00682-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/ec20bb5b15a2/biomedicines-09-00682-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/d35bc2e4ea7c/biomedicines-09-00682-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/4a7e0d508f75/biomedicines-09-00682-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/762bb6c2385d/biomedicines-09-00682-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/902bfce43e7c/biomedicines-09-00682-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/cce28b27a7e9/biomedicines-09-00682-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/ce84a3713704/biomedicines-09-00682-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/59887b47e282/biomedicines-09-00682-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/3eb19c9f11a3/biomedicines-09-00682-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/8a92b9ed3226/biomedicines-09-00682-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/bb2bff19cbf6/biomedicines-09-00682-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/6a628919e6cc/biomedicines-09-00682-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/753ea797030a/biomedicines-09-00682-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/ec20bb5b15a2/biomedicines-09-00682-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/d35bc2e4ea7c/biomedicines-09-00682-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/4a7e0d508f75/biomedicines-09-00682-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/762bb6c2385d/biomedicines-09-00682-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e071/8235213/902bfce43e7c/biomedicines-09-00682-g013.jpg

相似文献

1
Chronic Glaucoma Using Biodegradable Microspheres to Induce Intraocular Pressure Elevation. Six-Month Follow-Up.使用可生物降解微球诱导眼压升高治疗慢性青光眼。六个月随访
Biomedicines. 2021 Jun 16;9(6):682. doi: 10.3390/biomedicines9060682.
2
Long-term corticosteroid-induced chronic glaucoma model produced by intracameral injection of dexamethasone-loaded PLGA microspheres.经房水内注射载地塞米松 PLGA 微球制备的长期皮质类固醇诱导性慢性青光眼模型。
Drug Deliv. 2021 Dec;28(1):2427-2446. doi: 10.1080/10717544.2021.1998245.
3
Novel Use of PLGA Microspheres to Create an Animal Model of Glaucoma with Progressive Neuroretinal Degeneration.聚乳酸-羟基乙酸共聚物微球在创建进行性神经视网膜变性青光眼动物模型中的新应用
Pharmaceutics. 2021 Feb 8;13(2):237. doi: 10.3390/pharmaceutics13020237.
4
Influence of Sex on Neuroretinal Degeneration: Six-Month Follow-Up in Rats With Chronic Glaucoma.性别对神经视网膜变性的影响:慢性青光眼大鼠的六个月随访。
Invest Ophthalmol Vis Sci. 2021 Oct 4;62(13):9. doi: 10.1167/iovs.62.13.9.
5
Mimicking chronic glaucoma over 6 months with a single intracameral injection of dexamethasone/fibronectin-loaded PLGA microspheres.通过单次房内注射载有地塞米松/纤维连接蛋白的 PLGA 微球模拟慢性青光眼长达 6 个月。
Drug Deliv. 2022 Dec;29(1):2357-2374. doi: 10.1080/10717544.2022.2096712.
6
Chronic Glaucoma Induced in Rats by a Single Injection of Fibronectin-Loaded PLGA Microspheres: IOP-Dependent and IOP-Independent Neurodegeneration.载纤维连接蛋白的 PLGA 微球单次注射致大鼠慢性青光眼:IOP 依赖性和 IOP 非依赖性神经退行性变。
Int J Mol Sci. 2023 Dec 19;25(1):9. doi: 10.3390/ijms25010009.
7
Influence of sex on chronic steroid-induced glaucoma: 24-Weeks follow-up study in rats.性别对慢性类固醇诱导性青光眼的影响:大鼠 24 周随访研究。
Exp Eye Res. 2024 Jan;238:109736. doi: 10.1016/j.exer.2023.109736. Epub 2023 Nov 28.
8
Effect of age and sex on neurodevelopment and neurodegeneration in the healthy eye: Longitudinal functional and structural study in the Long-Evans rat.年龄和性别对健康眼中神经发育和神经退行性变的影响:Long-Evans 大鼠的纵向功能和结构研究。
Exp Eye Res. 2020 Nov;200:108208. doi: 10.1016/j.exer.2020.108208. Epub 2020 Aug 31.
9
Tunable degrees of neurodegeneration in rats based on microsphere-induced models of chronic glaucoma.基于微球诱导的慢性青光眼模型的大鼠可调控的神经退行性变程度。
Sci Rep. 2022 Nov 30;12(1):20622. doi: 10.1038/s41598-022-24954-4.
10
Intravitreal injections of GDNF-loaded biodegradable microspheres are neuroprotective in a rat model of glaucoma.玻璃体内注射载有胶质细胞源性神经营养因子(GDNF)的可生物降解微球在青光眼大鼠模型中具有神经保护作用。
Mol Vis. 2007 Sep 24;13:1783-92.

引用本文的文献

1
Mechanical property changes of glial LC and RGC axons in response to high intraocular pressure.胶质细胞终足和视网膜神经节细胞轴突在高眼压作用下的力学性能变化。
Front Bioeng Biotechnol. 2025 Apr 28;13:1574231. doi: 10.3389/fbioe.2025.1574231. eCollection 2025.
2
Multi-loaded PLGA microspheres as neuroretinal therapy in a chronic glaucoma animal model.多重负载的聚乳酸-羟基乙酸共聚物微球在慢性青光眼动物模型中作为神经视网膜治疗手段的应用
Drug Deliv Transl Res. 2025 May;15(5):1660-1684. doi: 10.1007/s13346-024-01702-x. Epub 2024 Oct 3.
3
Chronic Glaucoma Induced in Rats by a Single Injection of Fibronectin-Loaded PLGA Microspheres: IOP-Dependent and IOP-Independent Neurodegeneration.

本文引用的文献

1
Novel Use of PLGA Microspheres to Create an Animal Model of Glaucoma with Progressive Neuroretinal Degeneration.聚乳酸-羟基乙酸共聚物微球在创建进行性神经视网膜变性青光眼动物模型中的新应用
Pharmaceutics. 2021 Feb 8;13(2):237. doi: 10.3390/pharmaceutics13020237.
2
Effect of age and sex on neurodevelopment and neurodegeneration in the healthy eye: Longitudinal functional and structural study in the Long-Evans rat.年龄和性别对健康眼中神经发育和神经退行性变的影响:Long-Evans 大鼠的纵向功能和结构研究。
Exp Eye Res. 2020 Nov;200:108208. doi: 10.1016/j.exer.2020.108208. Epub 2020 Aug 31.
3
Astrocytes and microglia play orchestrated roles and respect phagocytic territories during neuronal corpse removal in vivo.
载纤维连接蛋白的 PLGA 微球单次注射致大鼠慢性青光眼:IOP 依赖性和 IOP 非依赖性神经退行性变。
Int J Mol Sci. 2023 Dec 19;25(1):9. doi: 10.3390/ijms25010009.
4
Three Major Causes of Metabolic Retinal Degenerations and Three Ways to Avoid Them.三大代谢性视网膜退行性疾病的病因及三种预防方法。
Int J Mol Sci. 2023 May 13;24(10):8728. doi: 10.3390/ijms24108728.
5
Intraocular nano-microscale drug delivery systems for glaucoma treatment: design strategies and recent progress.用于治疗青光眼的眼内纳微尺度药物输送系统:设计策略和最新进展。
J Nanobiotechnology. 2023 Mar 10;21(1):84. doi: 10.1186/s12951-023-01838-x.
6
Morphological Changes of Glial Lamina Cribrosa of Rats Suffering from Chronic High Intraocular Pressure.慢性高眼压大鼠筛板神经胶质层的形态学变化
Bioengineering (Basel). 2022 Nov 30;9(12):741. doi: 10.3390/bioengineering9120741.
7
Tunable degrees of neurodegeneration in rats based on microsphere-induced models of chronic glaucoma.基于微球诱导的慢性青光眼模型的大鼠可调控的神经退行性变程度。
Sci Rep. 2022 Nov 30;12(1):20622. doi: 10.1038/s41598-022-24954-4.
8
Mimicking chronic glaucoma over 6 months with a single intracameral injection of dexamethasone/fibronectin-loaded PLGA microspheres.通过单次房内注射载有地塞米松/纤维连接蛋白的 PLGA 微球模拟慢性青光眼长达 6 个月。
Drug Deliv. 2022 Dec;29(1):2357-2374. doi: 10.1080/10717544.2022.2096712.
9
Long-term and potent IOP-lowering effect of IκBα-siRNA in a nonhuman primate model of chronic ocular hypertension.IκBα小干扰RNA在慢性高眼压非人类灵长类动物模型中的长期强效降眼压作用
iScience. 2022 Mar 22;25(4):104149. doi: 10.1016/j.isci.2022.104149. eCollection 2022 Apr 15.
10
Analysis of Parainflammation in Chronic Glaucoma Using Vitreous-OCT Imaging.使用玻璃体光学相干断层扫描成像分析慢性青光眼的副炎症
Biomedicines. 2021 Nov 29;9(12):1792. doi: 10.3390/biomedicines9121792.
星形胶质细胞和小胶质细胞在体内神经元尸骸清除过程中发挥协调作用,并尊重吞噬作用领域。
Sci Adv. 2020 Jun 26;6(26):eaba3239. doi: 10.1126/sciadv.aba3239. eCollection 2020 Jun.
4
Rod bipolar cells dysfunction occurs before ganglion cells loss in excitotoxin-damaged mouse retina.杆状双极细胞功能障碍发生在兴奋性毒素损伤的小鼠视网膜中神经节细胞丢失之前。
Cell Death Dis. 2019 Dec 2;10(12):905. doi: 10.1038/s41419-019-2140-x.
5
Inflammasome Activation Induces Pyroptosis in the Retina Exposed to Ocular Hypertension Injury.炎性小体激活在暴露于高眼压损伤的视网膜中诱导细胞焦亡。
Front Mol Neurosci. 2019 Mar 13;12:36. doi: 10.3389/fnmol.2019.00036. eCollection 2019.
6
ISCEV extended protocol for the stimulus-response series for the dark-adapted full-field ERG b-wave.国际临床视觉电生理学会(ISCEV)关于暗适应全视野视网膜电图b波刺激-反应系列的扩展协议。
Doc Ophthalmol. 2019 Jun;138(3):217-227. doi: 10.1007/s10633-019-09687-6. Epub 2019 Mar 30.
7
Combination therapy and co-delivery strategies to optimize treatment of posterior segment neurodegenerative diseases.联合治疗和共递药策略以优化治疗后节段神经退行性疾病。
Drug Discov Today. 2019 Aug;24(8):1644-1653. doi: 10.1016/j.drudis.2019.03.022. Epub 2019 Mar 27.
8
Mouse model of ocular hypertension with retinal ganglion cell degeneration.青光眼伴视网膜神经节细胞变性的小鼠模型。
PLoS One. 2019 Jan 14;14(1):e0208713. doi: 10.1371/journal.pone.0208713. eCollection 2019.
9
Review of rodent hypertensive glaucoma models.啮齿动物高血压性青光眼模型的综述。
Acta Ophthalmol. 2019 May;97(3):e331-e340. doi: 10.1111/aos.13983. Epub 2018 Dec 13.
10
Commensal microflora-induced T cell responses mediate progressive neurodegeneration in glaucoma.共生微生物诱导的 T 细胞反应介导青光眼的进行性神经退行性变。
Nat Commun. 2018 Aug 10;9(1):3209. doi: 10.1038/s41467-018-05681-9.