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浆果提取物对蓝光诱导的ARPE-19细胞和小鼠视网膜损伤的保护作用。

Protective effects of berry extract on blue light-induced retinal damage in ARPE-19 cells and mouse retina.

作者信息

Cho Hye Mi, Lee Sang Jun, Choung Se-Young

机构信息

Department of Biomedical and Pharmaceutical Sciences, Graduate School, Kyung Hee University, Seoul, Republic of Korea.

Holistic Bio CO., Seongnam, Republic of Korea.

出版信息

J Ginseng Res. 2023 Jan;47(1):65-73. doi: 10.1016/j.jgr.2022.04.002. Epub 2022 Apr 18.

Abstract

BACKGROUND

Age-related macular degeneration (AMD) is a significant visual disease that induces impaired vision and irreversible blindness in the elderly. However, the effects of berry extract (GBE) on the retina have not been studied. Therefore, this study aimed to investigate the protective effects of GBE on blue light (BL)-induced retinal damage and elucidate its underlying mechanisms in human retinal pigment epithelial cells (ARPE-19 cells) and Balb/c retina.

METHODS

To investigate the effects and underlying mechanisms of GBE on retinal damage , we performed cell viability assay, pre-and post-treatment of sample, reactive oxygen species (ROS) assay, quantitative real-time PCR (qRT-PCR), and western immunoblotting using A2E-laden ARPE-19 cells with BL exposure. In addition, Balb/c mice were irradiated with BL to induce retinal degeneration and orally administrated with GBE (50, 100, 200 mg/kg). Using the harvested retina, we performed histological analysis (thickness of retinal layers), qRT-PCR, and western immunoblotting to elucidate the effects and mechanisms of GBE against retinal damage .

RESULTS

GBE significantly inhibited BL-induced cell damage in ARPE-19 cells by activating the SIRT1/PGC-1α pathway, regulating NF-kB translocation, caspase 3 activation, PARP cleavage, expressions of apoptosis-related factors (BAX/BCL-2, LC3-Ⅱ, and p62), and ROS production. Furthermore, GBE prevented BL-induced retinal degeneration by restoring the thickness of retinal layers and suppressed inflammation and apoptosis via regulation of NF-kB and SIRT1/PGC-1α pathway, cleavage of caspase 3 and PARP, and expressions of apoptosis-related factors .

CONCLUSIONS

GBE could be a potential agent to prevent dry AMD and progression to wet AMD.

摘要

背景

年龄相关性黄斑变性(AMD)是一种严重的视觉疾病,可导致老年人视力受损和不可逆失明。然而,浆果提取物(GBE)对视网膜的影响尚未得到研究。因此,本研究旨在探讨GBE对蓝光(BL)诱导的视网膜损伤的保护作用,并阐明其在人视网膜色素上皮细胞(ARPE-19细胞)和Balb/c视网膜中的潜在机制。

方法

为了研究GBE对视网膜损伤的影响及其潜在机制,我们使用暴露于BL的富含A2E的ARPE-19细胞进行了细胞活力测定、样品的预处理和后处理、活性氧(ROS)测定、定量实时PCR(qRT-PCR)和western免疫印迹。此外,用BL照射Balb/c小鼠以诱导视网膜变性,并口服给予GBE(50、100、200mg/kg)。使用收获的视网膜,我们进行了组织学分析(视网膜层厚度)、qRT-PCR和western免疫印迹,以阐明GBE对视网膜损伤的影响和机制。

结果

GBE通过激活SIRT1/PGC-1α途径、调节NF-κB易位、半胱天冬酶3激活、PARP裂解、凋亡相关因子(BAX/BCL-2、LC3-Ⅱ和p62)的表达以及ROS产生,显著抑制BL诱导的ARPE-19细胞损伤。此外,GBE通过恢复视网膜层厚度预防BL诱导的视网膜变性,并通过调节NF-κB和SIRT1/PGC-1α途径、半胱天冬酶3和PARP的裂解以及凋亡相关因子的表达来抑制炎症和凋亡。

结论

GBE可能是预防干性AMD和进展为湿性AMD的潜在药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ed6/9834005/02f74b91eae1/ga1.jpg

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