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Pemafibrate Protects Against Retinal Dysfunction in a Murine Model of Diabetic Retinopathy
Diabetic retinopathy (DR) is one of the leading causes of blindness globally. Retinal neuronal abnormalities occur in the early stage in DR. Therefore, maintaining retinal neuronal activity in DR may prevent vision loss. Previously, pemafibrate, a novel selective peroxisome proliferator-activated re...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503472/ https://www.ncbi.nlm.nih.gov/pubmed/32872333 http://dx.doi.org/10.3390/ijms21176243 |
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author | Tomita, Yohei Lee, Deokho Miwa, Yukihiro Jiang, Xiaoyan Ohta, Masayuki Tsubota, Kazuo Kurihara, Toshihide |
author_facet | Tomita, Yohei Lee, Deokho Miwa, Yukihiro Jiang, Xiaoyan Ohta, Masayuki Tsubota, Kazuo Kurihara, Toshihide |
author_sort | Tomita, Yohei |
collection | PubMed |
description | Diabetic retinopathy (DR) is one of the leading causes of blindness globally. Retinal neuronal abnormalities occur in the early stage in DR. Therefore, maintaining retinal neuronal activity in DR may prevent vision loss. Previously, pemafibrate, a novel selective peroxisome proliferator-activated receptor alpha modulator, was suggested as a promising drug in hypertriglyceridemia. However, the role of pemafibrate remains obscure in DR. Therefore, we aimed to unravel systemic and retinal changes by pemafibrate in diabetes. Adult mice were intraperitoneally injected with streptozotocin (STZ) to induce diabetes. After STZ injection, diet supplemented with pemafibrate was given to STZ-induced diabetic mice for 12 weeks. During the experiment period, body weight and blood glucose levels were examined. Electroretinography was performed to check the retinal neural function. After sacrifice, the retina, liver, and blood samples were subjected to molecular analyses. We found pemafibrate mildly improved blood glucose level as well as lipid metabolism, boosted liver function, increased serum fibroblast growth factor21 level, restored retinal functional deficits, and increased retinal synaptophysin protein expression in STZ-induced diabetic mice. Our present data suggest a promising pemafibrate therapy for the prevention of early DR by improving systemic metabolism and protecting retinal function. |
format | Online Article Text |
id | pubmed-7503472 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-75034722020-09-23 Pemafibrate Protects Against Retinal Dysfunction in a Murine Model of Diabetic Retinopathy Tomita, Yohei Lee, Deokho Miwa, Yukihiro Jiang, Xiaoyan Ohta, Masayuki Tsubota, Kazuo Kurihara, Toshihide Int J Mol Sci Article Diabetic retinopathy (DR) is one of the leading causes of blindness globally. Retinal neuronal abnormalities occur in the early stage in DR. Therefore, maintaining retinal neuronal activity in DR may prevent vision loss. Previously, pemafibrate, a novel selective peroxisome proliferator-activated receptor alpha modulator, was suggested as a promising drug in hypertriglyceridemia. However, the role of pemafibrate remains obscure in DR. Therefore, we aimed to unravel systemic and retinal changes by pemafibrate in diabetes. Adult mice were intraperitoneally injected with streptozotocin (STZ) to induce diabetes. After STZ injection, diet supplemented with pemafibrate was given to STZ-induced diabetic mice for 12 weeks. During the experiment period, body weight and blood glucose levels were examined. Electroretinography was performed to check the retinal neural function. After sacrifice, the retina, liver, and blood samples were subjected to molecular analyses. We found pemafibrate mildly improved blood glucose level as well as lipid metabolism, boosted liver function, increased serum fibroblast growth factor21 level, restored retinal functional deficits, and increased retinal synaptophysin protein expression in STZ-induced diabetic mice. Our present data suggest a promising pemafibrate therapy for the prevention of early DR by improving systemic metabolism and protecting retinal function. MDPI 2020-08-28 /pmc/articles/PMC7503472/ /pubmed/32872333 http://dx.doi.org/10.3390/ijms21176243 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Tomita, Yohei Lee, Deokho Miwa, Yukihiro Jiang, Xiaoyan Ohta, Masayuki Tsubota, Kazuo Kurihara, Toshihide Pemafibrate Protects Against Retinal Dysfunction in a Murine Model of Diabetic Retinopathy |
title | Pemafibrate Protects Against Retinal Dysfunction in a Murine Model of Diabetic Retinopathy |
title_full | Pemafibrate Protects Against Retinal Dysfunction in a Murine Model of Diabetic Retinopathy |
title_fullStr | Pemafibrate Protects Against Retinal Dysfunction in a Murine Model of Diabetic Retinopathy |
title_full_unstemmed | Pemafibrate Protects Against Retinal Dysfunction in a Murine Model of Diabetic Retinopathy |
title_short | Pemafibrate Protects Against Retinal Dysfunction in a Murine Model of Diabetic Retinopathy |
title_sort | pemafibrate protects against retinal dysfunction in a murine model of diabetic retinopathy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7503472/ https://www.ncbi.nlm.nih.gov/pubmed/32872333 http://dx.doi.org/10.3390/ijms21176243 |
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