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黄甘方通过JAK2/STAT3通路消除晚期氧化蛋白产物对晚期糖基化终末产物受体表达的差异调节的氧化应激作用。

Huang Gan Formula Eliminates the Oxidative Stress Effects of Advanced Oxidation Protein Products on the Divergent Regulation of the Expression of AGEs Receptors via the JAK2/STAT3 Pathway.

作者信息

Deng Quanwen, Bu Can, Mo Liqian, Lv Bin, Song Shaolian, Xiao Xiaoyan, Dan Guo, Yang Xixiao

机构信息

Department of Pharmacy, Nanfang Hospital, Southern Medical University, Guangzhou 510515, China.

Department of Pharmacy, Shenzhen Hospital, Southern Medical University, Shenzhen 518000, China.

出版信息

Evid Based Complement Alternat Med. 2017;2017:4520916. doi: 10.1155/2017/4520916. Epub 2017 Mar 30.

Abstract

Chronic kidney disease (CKD) has a high prevalence and low cure rate and represents a significant health issue. Oxidative stress is common in CKD due to metabolic disorders, inflammation, and impaired renal function changing normal proteins into advanced oxidation protein products (AOPPs). Huang Gan formula (HGF) is a new type of traditional Chinese herbal medicine. Although we previously investigated the protective effects of HGF against oxidative stress, the mechanism of HGF in CKD is still not fully understood. In this study, we used western blotting, quantitative polymerase chain reaction, and biochemical assays to show that HGF significantly decreased AOPP-induced oxidative stress damage. Moreover, the protective effects of HGF might be associated with upregulation of the advanced glycation end product receptor 1 (AGE-R1) and downregulation of the receptor for advance glycation end products (RAGE). Treatment with HGF and the Janus kinase 2 (JAK2) inhibitor, AG4-90, significantly attenuated AOPP-induced JAK2/STAT3 protein levels. These findings indicate that HGF inhibits AOPP-mediated biological responses by inactivating the JAK2/STAT3 pathway. In conclusion, HGF eliminated AOPP-induced effects in human mesangial cells (HMCs) by interrupting JAK2/STAT3 signaling, which altered RAGE/AGE-R1 expression and reduced oxidative stress in CKD.

摘要

慢性肾脏病(CKD)患病率高、治愈率低,是一个重大的健康问题。由于代谢紊乱、炎症以及肾功能受损导致正常蛋白质转变为晚期氧化蛋白产物(AOPPs),氧化应激在CKD中很常见。黄甘方(HGF)是一种新型的中药。尽管我们之前研究了HGF对氧化应激的保护作用,但HGF在CKD中的作用机制仍未完全阐明。在本研究中,我们使用蛋白质印迹法、定量聚合酶链反应和生化分析表明,HGF显著降低了AOPP诱导的氧化应激损伤。此外,HGF的保护作用可能与晚期糖基化终产物受体1(AGE-R1)的上调和晚期糖基化终产物受体(RAGE)的下调有关。用HGF和Janus激酶2(JAK2)抑制剂AG4-90处理可显著减弱AOPP诱导的JAK2/STAT3蛋白水平。这些发现表明,HGF通过使JAK2/STAT3信号通路失活来抑制AOPP介导的生物学反应。总之,HGF通过中断JAK2/STAT3信号传导消除了AOPP在人肾小球系膜细胞(HMCs)中的作用,这改变了RAGE/AGE-R1的表达并降低了CKD中的氧化应激。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d85/5390641/2297c6aecb0f/ECAM2017-4520916.001.jpg

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