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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。

Long-term corticosteroid-induced chronic glaucoma model produced by intracameral injection of dexamethasone-loaded PLGA microspheres.

机构信息

Department of Ophthalmology, Miguel Servet University Hospital, Zaragoza, Spain.

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

出版信息

Drug Deliv. 2021 Dec;28(1):2427-2446. doi: 10.1080/10717544.2021.1998245.

Abstract

PURPOSE

To evaluate a new chronic glaucoma model produced by intracameral injection of dexamethasone-loaded poly lactic-co-glycolic acid microspheres (Dex-PLGA-Ms) over six months.

METHODS

Healthy rats received two injections (at baseline and Week 4) of Dex-PLGA-Ms into the anterior chamber of the right eye. Clinical signs and intraocular pressure (IOP) were weekly recorded. The structure of the retina and optic nerve was evaluated using optical coherence tomography (OCT) every two weeks and functionally using dark- and light-adapted electroretinography at 0-12-24 weeks. Histological studies were also performed.

RESULTS

IOP progressively increased up to hypertension (23.22 ± 3.63 mmHg) in both eyes but did so later in left eyes. OCT quantified a decrease in full-thickness retina posterior pole (R), retinal-nerve-fiber layer (RNFL), and ganglion-cell layer (GCL) thickness up to 24 weeks. Right eyes showed higher neuroretinal thickness loss up to week 8. RNFL experienced the highest percentage thickness loss at the inferior-superior axis, while in GCL the inner sectors of the horizontal axis (Nasal-Temporal) suffered the greatest decrease in thickness. Retinal ganglion cell, photoreceptor, and intermediate cell functionality decreased over time. Increased deposition of collagen IV was also found in zonular fibers and the ciliary body.

CONCLUSIONS

This work shows the usefulness of drug delivery systems, not to treat pathology but to induce it. Only two injections of Dex-PLGA-Ms in the anterior chamber of rat eyes were enough to progressively create ocular hypertension and subsequent functional and structural neuroretinal degeneration, at least over 6 months.

摘要

目的

评估通过房内注射载有地塞米松的聚丙交酯-乙交酯微球(Dex-PLGA-Ms)长达 6 个月的新慢性青光眼模型。

方法

健康大鼠右眼前房接受两次 Dex-PLGA-Ms 注射(基线和第 4 周)。每周记录临床症状和眼内压(IOP)。每两周使用光学相干断层扫描(OCT)评估视网膜和视神经结构,在 0-12-24 周使用暗适应和明适应视网膜电图评估功能。还进行了组织学研究。

结果

IOP 逐渐升高直至高血压(双眼 23.22 ± 3.63mmHg),但左眼升高较晚。OCT 定量分析表明,全层视网膜后极(R)、视网膜神经纤维层(RNFL)和节细胞层(GCL)厚度直至 24 周下降。右眼神经视网膜厚度损失高达 8 周。RNFL 在下-上轴的厚度损失百分比最高,而在 GCL 中,水平轴的内区(鼻侧-颞侧)厚度下降最大。视网膜神经节细胞、光感受器和中间细胞的功能随时间降低。还发现带状纤维和睫状体中 IV 型胶原的沉积增加。

结论

这项工作表明,药物输送系统不仅可用于治疗疾病,还可用于诱导疾病。在大鼠眼前房内仅两次注射 Dex-PLGA-Ms 就足以逐渐产生眼内高压以及随后的功能性和结构性神经视网膜变性,至少在 6 个月以上。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b696/8592597/5f87bcd27f91/IDRD_A_1998245_F0001_C.jpg

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