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小梁网中的线粒体损伤仅发生于原发性开角型青光眼和假性剥脱性青光眼。

Mitochondrial damage in the trabecular meshwork occurs only in primary open-angle glaucoma and in pseudoexfoliative glaucoma.

机构信息

Department of Health Sciences, University of Genoa, Genoa, Italy.

出版信息

PLoS One. 2011 Jan 20;6(1):e14567. doi: 10.1371/journal.pone.0014567.

Abstract

BACKGROUND

Open-angle glaucoma appears to be induced by the malfunction of the trabecular meshwork cells due to injury induced by oxidative damage and mitochondrial impairment. Here, we report that, in fact, we have detected mitochondrial damage only in primary open-angle glaucoma and pseudo-exfoliation glaucoma, among several glaucoma types compared.

METHODOLOGY/PRINCIPAL FINDINGS: Mitochondrial damage was evaluated by analyzing the common mitochondrial DNA deletion by real-time PCR in trabecular meshwork specimens collected at surgery from glaucomatous patients and controls. Glaucomatous patients included 38 patients affected by various glaucoma types: primary open-angle, pigmented, juvenile, congenital, pseudoexfoliative, acute, neovascular, and chronic closed-angle glaucoma. As control samples, we used 16 specimens collected from glaucoma-free corneal donors. Only primary open-angle glaucoma (3.0-fold) and pseudoexfoliative glaucoma (6.3-fold) showed significant increases in the amount of mitochondrial DNA deletion. In all other cases, deletion was similar to controls.

CONCLUSIONS/SIGNIFICANCE: despite the fact that the trabecular meshwork is the most important tissue in the physiopathology of aqueous humor outflow in all glaucoma types, the present study provides new information regarding basic physiopathology of this tissue: only in primary open-angle and pseudoexfoliative glaucomas oxidative damage arising from mitochondrial failure play a role in the functional decay of trabecular meshwork.

摘要

背景

开角型青光眼似乎是由于小梁细胞的功能障碍引起的,这种功能障碍是由于氧化损伤和线粒体损伤引起的细胞损伤。在这里,我们报告说,事实上,我们仅在原发性开角型青光眼和假性剥脱性青光眼这两种青光眼类型中检测到了线粒体损伤,而在其他几种青光眼类型中并未检测到。

方法/主要发现:通过实时 PCR 分析小梁组织标本中常见的线粒体 DNA 缺失,评估线粒体损伤,这些标本是从手术中收集的青光眼患者和对照组的标本。青光眼患者包括 38 名患有各种青光眼类型的患者:原发性开角型、色素性、青少年型、先天性、假性剥脱性、急性、新生血管性和慢性闭角型青光眼。作为对照样本,我们使用了 16 个从无青光眼的角膜供体中收集的标本。只有原发性开角型青光眼(3.0 倍)和假性剥脱性青光眼(6.3 倍)显示出线粒体 DNA 缺失量的显著增加。在所有其他情况下,缺失与对照组相似。

结论/意义:尽管小梁是所有青光眼类型房水流出生理病理的最重要组织,但本研究提供了有关该组织基本生理病理的新信息:只有在原发性开角型和假性剥脱性青光眼中,由于线粒体功能衰竭引起的氧化损伤才会在小梁功能衰退中起作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2dd6/3024391/2a0d54d434b4/pone.0014567.g001.jpg

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