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Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model

Inhibition of fibrosis is indispensable for maintaining filtering blebs after glaucoma filtration surgery (GFS). The purpose of this study was to investigate the ability of a pluripotent epigenetic regulator OBP-801 (OBP) to ameliorate extracellular matrix formation in a rabbit model of GFS. Rabbits...

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Autores principales: Yamamoto, Yuji, Mukai, Atsushi, Ikushima, Toru, Urata, Yasuo, Kinoshita, Shigeru, Hamuro, Junji, Ueno, Morio, Sotozono, Chie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708845/
https://www.ncbi.nlm.nih.gov/pubmed/33262357
http://dx.doi.org/10.1038/s41598-020-77811-7
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author Yamamoto, Yuji
Mukai, Atsushi
Ikushima, Toru
Urata, Yasuo
Kinoshita, Shigeru
Hamuro, Junji
Ueno, Morio
Sotozono, Chie
author_facet Yamamoto, Yuji
Mukai, Atsushi
Ikushima, Toru
Urata, Yasuo
Kinoshita, Shigeru
Hamuro, Junji
Ueno, Morio
Sotozono, Chie
author_sort Yamamoto, Yuji
collection PubMed
description Inhibition of fibrosis is indispensable for maintaining filtering blebs after glaucoma filtration surgery (GFS). The purpose of this study was to investigate the ability of a pluripotent epigenetic regulator OBP-801 (OBP) to ameliorate extracellular matrix formation in a rabbit model of GFS. Rabbits that underwent GFS were treated with OBP. The gene expression profiles and intraocular pressure (IOP) were monitored until 30 postoperative days. The bleb tissues were evaluated for tissue fibrosis at 30 postoperative days. In in vitro models, OBP interfered the functions of diverse genes during the wound-healing process. In in vivo GFS models, the expressions of TGF-β3, MMP-2, TIMP-2 and 3, LOX, COL1A and SERPINH1 were significantly inhibited at 30 postoperative days in the OBP group compared with those in the vehicle control group. OBP treatment involving subconjunctival injection or eye drops showed no adverse effects, and reduced levels of α-SMA and collagen deposition at the surgical wound site. OBP maintained the long-lived bleb without scar formation, and IOP was lower at 30 postoperative days compared with the vehicle control group. These findings suggest that OBP is an effective and useful candidate low-molecular-weight agent for improving wound healing and surgical outcomes in a rabbit model of GFS.
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spelling pubmed-77088452020-12-03 Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model Yamamoto, Yuji Mukai, Atsushi Ikushima, Toru Urata, Yasuo Kinoshita, Shigeru Hamuro, Junji Ueno, Morio Sotozono, Chie Sci Rep Article Inhibition of fibrosis is indispensable for maintaining filtering blebs after glaucoma filtration surgery (GFS). The purpose of this study was to investigate the ability of a pluripotent epigenetic regulator OBP-801 (OBP) to ameliorate extracellular matrix formation in a rabbit model of GFS. Rabbits that underwent GFS were treated with OBP. The gene expression profiles and intraocular pressure (IOP) were monitored until 30 postoperative days. The bleb tissues were evaluated for tissue fibrosis at 30 postoperative days. In in vitro models, OBP interfered the functions of diverse genes during the wound-healing process. In in vivo GFS models, the expressions of TGF-β3, MMP-2, TIMP-2 and 3, LOX, COL1A and SERPINH1 were significantly inhibited at 30 postoperative days in the OBP group compared with those in the vehicle control group. OBP treatment involving subconjunctival injection or eye drops showed no adverse effects, and reduced levels of α-SMA and collagen deposition at the surgical wound site. OBP maintained the long-lived bleb without scar formation, and IOP was lower at 30 postoperative days compared with the vehicle control group. These findings suggest that OBP is an effective and useful candidate low-molecular-weight agent for improving wound healing and surgical outcomes in a rabbit model of GFS. Nature Publishing Group UK 2020-12-01 /pmc/articles/PMC7708845/ /pubmed/33262357 http://dx.doi.org/10.1038/s41598-020-77811-7 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Yamamoto, Yuji
Mukai, Atsushi
Ikushima, Toru
Urata, Yasuo
Kinoshita, Shigeru
Hamuro, Junji
Ueno, Morio
Sotozono, Chie
Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
title Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
title_full Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
title_fullStr Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
title_full_unstemmed Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
title_short Pluripotent epigenetic regulator OBP-801 maintains filtering blebs in glaucoma filtration surgery model
title_sort pluripotent epigenetic regulator obp-801 maintains filtering blebs in glaucoma filtration surgery model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7708845/
https://www.ncbi.nlm.nih.gov/pubmed/33262357
http://dx.doi.org/10.1038/s41598-020-77811-7
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