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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.

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/cce28b27a7e9/biomedicines-09-00682-g001.jpg

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