| Literature DB >> 31202173 |
Mao-Mao Zhu1, Long Wang2, Dang Yang3, Chao Li4, Shi-Ting Pang2, Xing-Hua Li2, Ru Li2, Bing Yang3, Yuan-Pei Lian2, Liang Ma3, Qing-Lin Lv2, Xiao-Bin Jia5, Liang Feng6.
Abstract
The acute kidney injury(AKI) caused by nephrotoxic drugs contributes to inflammation and oxidative injury in podocytes. Wedelolactone (WED), a natural compound, is found with activities as anti-inflammation, anti-oxidative, anti-free radical,and etc. In this present study, MPC-5 cells were exposed to the nephrotoxic drugs doxorubicin (DOX). The results showed that WED significantly increased the SOD activity, CAT and GSH-Px levels, while significantly decreased the MDA content and ROS levels in DOX-induced MPC-5 cells. WED could also significantly decrease the levels of cytokines IL-6, MCP-1, TNF-α, and TGF-β1. Additionally, the activation and phosphorylation of IκKα, IκBα and NF-κB p65 was inhibited by WED. The co-treatment of PDTC (NF-κB inhibitor) and WED significantly reduced NF-κB p65 phosphorylation. These findings suggested that WED alleviated inflammation and oxidative stress of doxorubicin-induced MPC-5 cells through IκK/IκB/NF-κB signaling pathway.Entities:
Keywords: Doxorubicin; Inflammation; Oxidative stress; Podocyte; Wedelolactone
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Year: 2019 PMID: 31202173 DOI: 10.1016/j.biopha.2019.109088
Source DB: PubMed Journal: Biomed Pharmacother ISSN: 0753-3322 Impact factor: 6.529