Fibroblast Growth Factor Type 1 Ameliorates High-Glucose-Induced Oxidative Stress and Neuroinflammation in Retinal Pigment Epithelial Cells and a Streptozotocin-Induced Diabetic Rat Model

Diabetic retinopathy (DR) is a common complication of diabetes that causes severe visual impairment globally. The pathogenesis of DR is related to oxidative stress and chronic inflammation. The fibroblast growth factor type 1 (FGF-1) mitogen plays crucial roles in cell function, development, and met...

Full description

Bibliographic Details
Main Authors: Hsin-Wei Huang, Chung-May Yang, Chang-Hao Yang
Format: Article
Language:English
Published: MDPI AG 2021-07-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/13/7233
_version_ 1797528011105370112
author Hsin-Wei Huang
Chung-May Yang
Chang-Hao Yang
author_facet Hsin-Wei Huang
Chung-May Yang
Chang-Hao Yang
author_sort Hsin-Wei Huang
collection DOAJ
description Diabetic retinopathy (DR) is a common complication of diabetes that causes severe visual impairment globally. The pathogenesis of DR is related to oxidative stress and chronic inflammation. The fibroblast growth factor type 1 (FGF-1) mitogen plays crucial roles in cell function, development, and metabolism. FGF-1 is involved in blood sugar regulation and exerts beneficial antioxidative and anti-inflammatory effects on various organ systems. This study investigated the antioxidative and anti-inflammatory neuroprotective effects of FGF-1 on high-glucose-induced retinal damage. The results revealed that FGF-1 treatment significantly reversed the harmful effects of oxidative stress and inflammatory mediators in retinal tissue in a streptozotocin-induced diabetic rat model. These protective effects were also observed in the in vitro model of retinal ARPE-19 cells exposed to a high-glucose condition. We demonstrated that FGF-1 attenuated p38 mitogen-activated protein kinase and nuclear factor-κB pathway activation under the high-glucose condition. Our results indicated that FGF-1 could effectively prevent retinal injury in diabetes. The findings of this study could be used to develop novel treatments for DR that aim to reduce the cascade of oxidative stress and inflammatory signals in neuroretinal tissue.
first_indexed 2024-03-10T09:52:02Z
format Article
id doaj.art-afce117300834a2c9be11684447fecdf
institution Directory Open Access Journal
issn 1661-6596
1422-0067
language English
last_indexed 2024-03-10T09:52:02Z
publishDate 2021-07-01
publisher MDPI AG
record_format Article
series International Journal of Molecular Sciences
spelling doaj.art-afce117300834a2c9be11684447fecdf2023-11-22T02:42:41ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-07-012213723310.3390/ijms22137233Fibroblast Growth Factor Type 1 Ameliorates High-Glucose-Induced Oxidative Stress and Neuroinflammation in Retinal Pigment Epithelial Cells and a Streptozotocin-Induced Diabetic Rat ModelHsin-Wei Huang0Chung-May Yang1Chang-Hao Yang2Department of Ophthalmology, Wan Fang Hospital, Taipei Medical University, No. 111, Sec. 3, Xinglong Rd., Taipei 11696, TaiwanDepartment of Ophthalmology, National Taiwan University Hospital, No. 7, Zhongshan South Road, Taipei 100, TaiwanDepartment of Ophthalmology, National Taiwan University Hospital, No. 7, Zhongshan South Road, Taipei 100, TaiwanDiabetic retinopathy (DR) is a common complication of diabetes that causes severe visual impairment globally. The pathogenesis of DR is related to oxidative stress and chronic inflammation. The fibroblast growth factor type 1 (FGF-1) mitogen plays crucial roles in cell function, development, and metabolism. FGF-1 is involved in blood sugar regulation and exerts beneficial antioxidative and anti-inflammatory effects on various organ systems. This study investigated the antioxidative and anti-inflammatory neuroprotective effects of FGF-1 on high-glucose-induced retinal damage. The results revealed that FGF-1 treatment significantly reversed the harmful effects of oxidative stress and inflammatory mediators in retinal tissue in a streptozotocin-induced diabetic rat model. These protective effects were also observed in the in vitro model of retinal ARPE-19 cells exposed to a high-glucose condition. We demonstrated that FGF-1 attenuated p38 mitogen-activated protein kinase and nuclear factor-κB pathway activation under the high-glucose condition. Our results indicated that FGF-1 could effectively prevent retinal injury in diabetes. The findings of this study could be used to develop novel treatments for DR that aim to reduce the cascade of oxidative stress and inflammatory signals in neuroretinal tissue.https://www.mdpi.com/1422-0067/22/13/7233fibroblast growth factor type 1diabetic retinopathyoxidative stressinflammatory mediatorp38 mitogen-activated kinasenuclear factor-κB
spellingShingle Hsin-Wei Huang
Chung-May Yang
Chang-Hao Yang
Fibroblast Growth Factor Type 1 Ameliorates High-Glucose-Induced Oxidative Stress and Neuroinflammation in Retinal Pigment Epithelial Cells and a Streptozotocin-Induced Diabetic Rat Model
International Journal of Molecular Sciences
fibroblast growth factor type 1
diabetic retinopathy
oxidative stress
inflammatory mediator
p38 mitogen-activated kinase
nuclear factor-κB
title Fibroblast Growth Factor Type 1 Ameliorates High-Glucose-Induced Oxidative Stress and Neuroinflammation in Retinal Pigment Epithelial Cells and a Streptozotocin-Induced Diabetic Rat Model
title_full Fibroblast Growth Factor Type 1 Ameliorates High-Glucose-Induced Oxidative Stress and Neuroinflammation in Retinal Pigment Epithelial Cells and a Streptozotocin-Induced Diabetic Rat Model
title_fullStr Fibroblast Growth Factor Type 1 Ameliorates High-Glucose-Induced Oxidative Stress and Neuroinflammation in Retinal Pigment Epithelial Cells and a Streptozotocin-Induced Diabetic Rat Model
title_full_unstemmed Fibroblast Growth Factor Type 1 Ameliorates High-Glucose-Induced Oxidative Stress and Neuroinflammation in Retinal Pigment Epithelial Cells and a Streptozotocin-Induced Diabetic Rat Model
title_short Fibroblast Growth Factor Type 1 Ameliorates High-Glucose-Induced Oxidative Stress and Neuroinflammation in Retinal Pigment Epithelial Cells and a Streptozotocin-Induced Diabetic Rat Model
title_sort fibroblast growth factor type 1 ameliorates high glucose induced oxidative stress and neuroinflammation in retinal pigment epithelial cells and a streptozotocin induced diabetic rat model
topic fibroblast growth factor type 1
diabetic retinopathy
oxidative stress
inflammatory mediator
p38 mitogen-activated kinase
nuclear factor-κB
url https://www.mdpi.com/1422-0067/22/13/7233
work_keys_str_mv AT hsinweihuang fibroblastgrowthfactortype1ameliorateshighglucoseinducedoxidativestressandneuroinflammationinretinalpigmentepithelialcellsandastreptozotocininduceddiabeticratmodel
AT chungmayyang fibroblastgrowthfactortype1ameliorateshighglucoseinducedoxidativestressandneuroinflammationinretinalpigmentepithelialcellsandastreptozotocininduceddiabeticratmodel
AT changhaoyang fibroblastgrowthfactortype1ameliorateshighglucoseinducedoxidativestressandneuroinflammationinretinalpigmentepithelialcellsandastreptozotocininduceddiabeticratmodel