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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...

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Autores principales: Tomita, Yohei, Lee, Deokho, Miwa, Yukihiro, Jiang, Xiaoyan, Ohta, Masayuki, Tsubota, Kazuo, Kurihara, Toshihide
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
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.
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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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