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Periocular injection of candesartan-PLGA microparticles inhibits laser-induced experimental choroidal neovascularization

PURPOSE: Microparticle technology enables local administration of medication. The purpose of this study was to examine the inhibitory effect of locally administered candesartan (CAN)-encapsulated microparticles on experimental choroidal neovascularization (CNV). METHODS: Laser photocoagulation was u...

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Autores principales: Okuda, Yoshitaka, Fukumoto, Masanori, Horie, Taeko, Oku, Hidehiro, Takai, Shinji, Nakanishi, Toyofumi, Matsuzaki, Kaori, Tsujimoto, Hiroyuki, Ikeda, Tsunehiko
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318708/
https://www.ncbi.nlm.nih.gov/pubmed/30643382
http://dx.doi.org/10.2147/OPTH.S181110
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author Okuda, Yoshitaka
Fukumoto, Masanori
Horie, Taeko
Oku, Hidehiro
Takai, Shinji
Nakanishi, Toyofumi
Matsuzaki, Kaori
Tsujimoto, Hiroyuki
Ikeda, Tsunehiko
author_facet Okuda, Yoshitaka
Fukumoto, Masanori
Horie, Taeko
Oku, Hidehiro
Takai, Shinji
Nakanishi, Toyofumi
Matsuzaki, Kaori
Tsujimoto, Hiroyuki
Ikeda, Tsunehiko
author_sort Okuda, Yoshitaka
collection PubMed
description PURPOSE: Microparticle technology enables local administration of medication. The purpose of this study was to examine the inhibitory effect of locally administered candesartan (CAN)-encapsulated microparticles on experimental choroidal neovascularization (CNV). METHODS: Laser photocoagulation was used to induce CNV in Brown Norway rats. The rats were pretreated with subconjunctival injections of CAN (5.0 mg/eye) or phosphate buffer saline for 3 days before photocoagulation. The volume of CNV was evaluated 7 days after laser injury using the lectin staining technique. The infiltration of macrophages within the CNV lesion was determined using immunofluorescent staining with an anti-CD68 antibody. mRNA levels of MCP-1, IL1-β and VEGF in the retinal pigment epithelium/choroid complex were determined using quantitative PCR (q-PCR). RESULTS: CNV volume was significantly suppressed by the treatment with CAN compared with that in vehicle-treated eyes (P<0.05, two-tailed Student’s t-test). Subconjunctival injections of CAN decreased the numbers of CD68(+) cells in the CNV lesion. The increased mRNA levels of MCP-1, IL1-β, and VEGF induced by photocoagulation was significantly suppressed following the local administration of CAN (P<0.05, two-tailed Student’s t-test). CONCLUSION: Local administration of CAN inhibited experimentally induced CNV possibly through anti-inflammatory effects.
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spelling pubmed-63187082019-01-14 Periocular injection of candesartan-PLGA microparticles inhibits laser-induced experimental choroidal neovascularization Okuda, Yoshitaka Fukumoto, Masanori Horie, Taeko Oku, Hidehiro Takai, Shinji Nakanishi, Toyofumi Matsuzaki, Kaori Tsujimoto, Hiroyuki Ikeda, Tsunehiko Clin Ophthalmol Original Research PURPOSE: Microparticle technology enables local administration of medication. The purpose of this study was to examine the inhibitory effect of locally administered candesartan (CAN)-encapsulated microparticles on experimental choroidal neovascularization (CNV). METHODS: Laser photocoagulation was used to induce CNV in Brown Norway rats. The rats were pretreated with subconjunctival injections of CAN (5.0 mg/eye) or phosphate buffer saline for 3 days before photocoagulation. The volume of CNV was evaluated 7 days after laser injury using the lectin staining technique. The infiltration of macrophages within the CNV lesion was determined using immunofluorescent staining with an anti-CD68 antibody. mRNA levels of MCP-1, IL1-β and VEGF in the retinal pigment epithelium/choroid complex were determined using quantitative PCR (q-PCR). RESULTS: CNV volume was significantly suppressed by the treatment with CAN compared with that in vehicle-treated eyes (P<0.05, two-tailed Student’s t-test). Subconjunctival injections of CAN decreased the numbers of CD68(+) cells in the CNV lesion. The increased mRNA levels of MCP-1, IL1-β, and VEGF induced by photocoagulation was significantly suppressed following the local administration of CAN (P<0.05, two-tailed Student’s t-test). CONCLUSION: Local administration of CAN inhibited experimentally induced CNV possibly through anti-inflammatory effects. Dove Medical Press 2018-12-31 /pmc/articles/PMC6318708/ /pubmed/30643382 http://dx.doi.org/10.2147/OPTH.S181110 Text en © 2019 Okuda et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Original Research
Okuda, Yoshitaka
Fukumoto, Masanori
Horie, Taeko
Oku, Hidehiro
Takai, Shinji
Nakanishi, Toyofumi
Matsuzaki, Kaori
Tsujimoto, Hiroyuki
Ikeda, Tsunehiko
Periocular injection of candesartan-PLGA microparticles inhibits laser-induced experimental choroidal neovascularization
title Periocular injection of candesartan-PLGA microparticles inhibits laser-induced experimental choroidal neovascularization
title_full Periocular injection of candesartan-PLGA microparticles inhibits laser-induced experimental choroidal neovascularization
title_fullStr Periocular injection of candesartan-PLGA microparticles inhibits laser-induced experimental choroidal neovascularization
title_full_unstemmed Periocular injection of candesartan-PLGA microparticles inhibits laser-induced experimental choroidal neovascularization
title_short Periocular injection of candesartan-PLGA microparticles inhibits laser-induced experimental choroidal neovascularization
title_sort periocular injection of candesartan-plga microparticles inhibits laser-induced experimental choroidal neovascularization
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6318708/
https://www.ncbi.nlm.nih.gov/pubmed/30643382
http://dx.doi.org/10.2147/OPTH.S181110
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