Novel Therapeutic Effects of Euphorbia heterophylla L. Methanol Extracts in Macular Degeneration Caused by Blue Light in A2E-Laden ARPE-19 Cells and Retina of BALB/c Mice

Bibliographic Details
Title: Novel Therapeutic Effects of Euphorbia heterophylla L. Methanol Extracts in Macular Degeneration Caused by Blue Light in A2E-Laden ARPE-19 Cells and Retina of BALB/c Mice
Authors: Ayun Seol, Ji-Eun Kim, You-Jeong Jin, Hee-Jin Song, Yu-Jeong Roh, Tae-Ryeol Kim, Eun-Seo Park, Ki-Ho Park, So-Hae Park, Muhammad Salah Uddin, Sang-Woo Lee, Young-Woo Choi, Dae-Youn Hwang
Source: Pharmaceuticals, Vol 17, Iss 9, p 1193 (2024)
Publisher Information: MDPI AG, 2024.
Publication Year: 2024
Collection: LCC:Medicine
LCC:Pharmacy and materia medica
Subject Terms: Euphorbia heterophylla L., age-related macular degeneration, retina, oxidative stress, BALB/c mice, Medicine, Pharmacy and materia medica, RS1-441
More Details: Natural products with high antioxidant activity are considered as innovative prevention strategies to effectively prevent age-related macular degeneration (AMD) in the early stage because the generation of reactive oxygen species (ROS) leading to the development of drusen is reported as an important cause of this disease. To investigate the prevention effects of the methanol extracts of Euphorbia heterophylla L. (MEE) on AMD, its effects on the antioxidant activity, inflammatory response, apoptosis pathway, neovascularization, and retinal tissue degeneration were analyzed in N-retinylidene-N-retinylethanolamine (A2E)-landed spontaneously arising retinal pigment epithelia (ARPE)-19 cells and BALB/c mice after exposure to blue light (BL). The MEE contained 10 active components and showed high free radical scavenging activity against 2,2-diphenyl-1-picrylhydrazyl (DPPH), 2,2′-azino-bis (3-ethylbenzothiazoline-6-sulfonic acid) (ABTS), and nitric oxide (NO) radicals. The pretreatments of high-dose MEE remarkably suppressed the production of intracellular ROS (88.2%) and NO (25.2%) and enhanced (SOD) activity (84%) and the phosphorylation of nuclear factor erythroid 2–related factor 2 (Nrf2) in A2E + BL-treated ARPE-19 cells compared to Vehicle-treated group. The activation of the inducible nitric oxide synthase (iNOS)-induced cyclooxygenase-2 (COX-2) mediated pathway, inflammasome activation, and expression of inflammatory cytokines was significantly inhibited in A2E + BL-treated ARPE-19 cells after the MEE pretreatment. The activation of the apoptosis pathway and increased expression of neovascular proteins (36% for matrix metalloproteinase (MMP)-9) were inhibited in the MEE pretreated groups compared to the Vehicle-treated group. Furthermore, the thickness of the whole retina (31%), outer nuclear layer (ONL), inner nuclear layer (INL), and photoreceptor layer (PL) were significantly increased by the MEE pretreatment of BALB/c mice with BL-induced retinal degeneration. Therefore, these results suggest that the MEE, with its high antioxidative activity, protects against BL-induced retinal degeneration through the regulation of the antioxidative system, inflammatory response, apoptosis, and neovascularization in the AMD mouse model.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 1424-8247
Relation: https://www.mdpi.com/1424-8247/17/9/1193; https://doaj.org/toc/1424-8247
DOI: 10.3390/ph17091193
Access URL: https://doaj.org/article/2a7e2d7b3eea4d889f7130d043ddef94
Accession Number: edsdoj.2a7e2d7b3eea4d889f7130d043ddef94
Database: Directory of Open Access Journals
Full text is not displayed to guests.
More Details
ISSN:14248247
DOI:10.3390/ph17091193
Published in:Pharmaceuticals
Language:English