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Wedelolactone alleviates doxorubicin-induced inflammation and oxidative stress damage of podocytes by IκK/IκB/NF-κB pathway.
- Source :
-
Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie [Biomed Pharmacother] 2019 Sep; Vol. 117, pp. 109088. Date of Electronic Publication: 2019 Jun 12. - Publication Year :
- 2019
-
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.<br /> (Copyright © 2019 The Authors. Published by Elsevier Masson SAS.. All rights reserved.)
- Subjects :
- Animals
Cell Line
I-kappa B Proteins metabolism
Inflammation metabolism
Mice
NF-KappaB Inhibitor alpha metabolism
NF-kappa B metabolism
Phosphorylation drug effects
Podocytes metabolism
Rats
Transcription Factor RelA metabolism
Tumor Necrosis Factor-alpha metabolism
Coumarins pharmacology
Doxorubicin pharmacology
Inflammation chemically induced
Inflammation drug therapy
Oxidative Stress drug effects
Podocytes drug effects
Signal Transduction drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 1950-6007
- Volume :
- 117
- Database :
- MEDLINE
- Journal :
- Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie
- Publication Type :
- Academic Journal
- Accession number :
- 31202173
- Full Text :
- https://doi.org/10.1016/j.biopha.2019.109088