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α-山竹黄酮对氧化应激诱导的视网膜细胞死亡的保护作用。

Protective effect of alpha-mangostin against oxidative stress induced-retinal cell death.

作者信息

Fang Yuan, Su Tu, Qiu Xiaorong, Mao Pingan, Xu Yidan, Hu Zizhong, Zhang Yi, Zheng Xinhua, Xie Ping, Liu Qinghuai

机构信息

Department of Ophthalmology, The First Affiliated Hospital of Nanjing Medical University, Nanjing, Jiangsu 210029, China.

出版信息

Sci Rep. 2016 Feb 18;6:21018. doi: 10.1038/srep21018.

Abstract

It is known that oxidative stress plays a pivotal role in age-related macular degeneration (AMD) pathogenesis. Alpha-mangostin is the main xanthone purified from mangosteen known as anti-oxidative properties. The aim of the study was to test the protective effect of alpha-mangostin against oxidative stress both in retina of light-damaged mice model and in hydrogen peroxide (H2O2)-stressed RPE cells. We observed that alpha-mangostin significantly inhibited light-induced degeneration of photoreceptors and 200 μM H2O2-induced apoptosis of RPE cells. 200 μM H2O2-induced generation of reactive oxygen species (ROS) and light-induced generation of malondialdehyde (MDA) were suppressed by alpha-mangostin. Alpha-mangostin stimulation resulted in an increase of superoxide dismutase (SOD) activity, glutathione peroxidase (GPX) activity and glutathione (GSH) content both in vivo and vitro. Furthermore, the mechanism of retinal protection against oxidative stress by alpha-mangostin involves accumulation and the nuclear translocation of the NF-E2-related factor (Nrf2) along with up-regulation the expression of heme oxygenas-1 (HO-1). Meanwhile, alpha-mangostin can activate the expression of PKC-δ and down-regulate the expression of mitogen-activated protein kinases (MAPKs), including ERK1/2, JNK, P38. The results suggest that alpha-mangostin could be a new approach to suspend the onset and development of AMD.

摘要

众所周知,氧化应激在年龄相关性黄斑变性(AMD)的发病机制中起关键作用。α-山竹黄酮是从山竹果中纯化得到的主要氧杂蒽酮,具有抗氧化特性。本研究的目的是在光损伤小鼠模型的视网膜和过氧化氢(H2O2)应激的视网膜色素上皮(RPE)细胞中测试α-山竹黄酮对氧化应激的保护作用。我们观察到,α-山竹黄酮显著抑制光诱导的光感受器变性以及200μM H2O2诱导的RPE细胞凋亡。α-山竹黄酮抑制了200μM H2O2诱导的活性氧(ROS)生成以及光诱导的丙二醛(MDA)生成。α-山竹黄酮刺激导致体内和体外超氧化物歧化酶(SOD)活性、谷胱甘肽过氧化物酶(GPX)活性和谷胱甘肽(GSH)含量增加。此外,α-山竹黄酮对视网膜氧化应激的保护机制涉及NF-E2相关因子(Nrf2)的积累和核转位以及血红素加氧酶-1(HO-1)表达的上调。同时,α-山竹黄酮可激活蛋白激酶C-δ(PKC-δ)的表达并下调丝裂原活化蛋白激酶(MAPK)的表达,包括细胞外信号调节激酶1/2(ERK1/2)、c-Jun氨基末端激酶(JNK)、p38。结果表明,α-山竹黄酮可能是延缓AMD发病和发展的一种新方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4051/4757868/dd2b6cb27eab/srep21018-f1.jpg

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