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The regulation of Kir4.1 by pigment epithelium-derived factor in Müller cells under high glucose conditions / 中华眼底病杂志
Chinese Journal of Ocular Fundus Diseases ; (6): 268-271, 2012.
Artigo em Chinês | WPRIM | ID: wpr-428775
ABSTRACT
ObjectiveTo investigate Kir4.1 expressions in Müller cells under high glucose conditions and treatment of pigment epithelium derived factor (PEDF).Methods Cultured rat Müller cells were divided into control group (5 mmol/L glucose),high glucose group (25 mmol/L glucose),PEDF treatment group (25 mmol/L glucose+ 100 ng/ml PEDF) and intervention control group(25 mmol/L glucose +phosphate buffer solution). Kir4.1 expressions were measured by Western blot and real-time reverse transcription polymerase chain reaction (RT-PCR). Reactive oxygen species (ROS) productions were measured using 2′7′-dichlorofluorescin diacetate and glutathione peroxidase (GPx)expressions were studied by real-time RT-PCR.ResultsBy Western blot and real-time RT-PCR,it was found the expressions of Kir4.1 decreased obviously under high glucose conditions (real-time RT-PCRt=4.12,P<0.05; Western blott=3.53,P<0.05) ; simultaneously,ROS generation was increased (t=3.76,P<0.05) and GPx level was decreased (t=3.18,P<0.05).PEDF treatment inhibited the high glucose-induced Kir4.1 down regulation (real-time RT-PCRt =3.66,P<0.05 ; Western blott =6.43,P<0,01 ) and decreased ROS generations (t=4.11,P<0.05) and increased GPx levels (t=5.12,P<0.01).ConclusionsThe high glucose can supress Kir4.1 expressions in Müller cells by oxidative stress,and PEDF can ameliorate these effects.

Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Idioma: Chinês Revista: Chinese Journal of Ocular Fundus Diseases Ano de publicação: 2012 Tipo de documento: Artigo

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Texto completo: DisponíveL Índice: WPRIM (Pacífico Ocidental) Idioma: Chinês Revista: Chinese Journal of Ocular Fundus Diseases Ano de publicação: 2012 Tipo de documento: Artigo