Fenofibrate ameliorates diabetic retinopathy by modulating Nrf2 signaling and NLRP3 inflammasome activation

Oxidative stress and neuroinflammation contribute significantly to the development and progression of diabetic retinopathy. Fenofibrate has received great attention as it benefits diabetic patients by reducing retinal laser requirement. Nuclear factor erythroid-2-related factor 2 (Nrf2) is a master...

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Vydáno v:Molecular and cellular biochemistry Ročník 445; číslo 1-2; s. 105 - 115
Hlavní autoři: Liu, Qiuping, Zhang, Fengjun, Zhang, Xian, Cheng, Rui, Ma, Jian-xing, Yi, Jinglin, Li, Jingming
Médium: Journal Article
Jazyk:angličtina
Vydáno: New York Springer US 01.08.2018
Springer
Springer Nature B.V
Témata:
Activation
Biochemistry
Biomedical and Life Sciences
Cardiology
Caspase
Caspase-1
Diabetes
Diabetes mellitus
Diabetic retinopathy
Diabetics
Fenofibrate
Fibric acids
Gene expression
Glutamate-ammonia ligase
Glutamine
IL-1β
Inflammasomes
Inflammation
Intercellular adhesion molecule 1
Leakage
Leucine
Life Sciences
Medical Biochemistry
Mice
NRF2 protein
Oncology
Oxidative stress
Pyrin protein
Reactive oxygen species
Retina
Retinopathy
Rodents
Signaling
Streptozocin
Fenofibrate
Diabetic retinopathy
Oxidative stress
Inflammasome
ISSN:0300-8177, 1573-4919, 1573-4919
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Shrnutí:Oxidative stress and neuroinflammation contribute significantly to the development and progression of diabetic retinopathy. Fenofibrate has received great attention as it benefits diabetic patients by reducing retinal laser requirement. Nuclear factor erythroid-2-related factor 2 (Nrf2) is a master regulator of anti-oxidative defense. Activation of nucleotide binding domain, leucine-rich repeat-containing receptor (NLR), pyrin domain-containing 3 (NLRP3) inflammasome plays a pivotal role in neuroinflammation. The purpose of this study is to determine whether fenofibrate protects retinas from oxidative damage and neuroinflammation via modulating the Nrf2 pathway and blocking NLRP3 inflammasome activation during diabetes. Diabetes is induced by intraperitoneal injection of streptozotocin in mice. Fenofibrate was given to mice in rodent chow. Upregulation of Nrf2 and NLRP3 inflammasome, enhanced ROS formation, and increased leukostasis and vascular leakage were observed in diabetic mouse retinas. Notably, Nrf2 and Caspase-1 were mainly colocalized with glutamine synthetase, one of the Mȕller cell markers. Fenofibrate further increased the expression of Nrf2 and its target gene NQO-1 and HO-1 and reduced ROS formation in diabetic retinas. In addition, retinal expression of NLRP3, Caspase-1 p20, IL-1β p17, and ICAM-1 were dramatically increased in vehicle-treated diabetic mice, which were abolished by fenofibrate intervention. Moreover, fenofibrate treatment also attenuated diabetes-induced retinal leukostasis and vascular leakage in mice. Taken together, fenofibrate attenuates oxidative stress and neuroinflammation in diabetic retinas, which is at least partially through modulating Nrf2 expression and NLRP3 inflammasome activation.
Bibliografie:ObjectType-Article-1
SourceType-Scholarly Journals-1
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ISSN:0300-8177
1573-4919
1573-4919
DOI:10.1007/s11010-017-3256-x