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A polysaccharide from Huaier ameliorates cisplatin nephrotoxicity by decreasing oxidative stress and apoptosis via PI3K/AKT signaling.

Authors :
Fang, Liang
Zhang, Yongzhen
Wang, Qi
Zang, Yuanwei
Li, Zeyan
Duan, Zhichen
Ren, Juchao
Xu, Zhonghua
Source :
International Journal of Biological Macromolecules. Oct2019, Vol. 139, p932-943. 12p.
Publication Year :
2019

Abstract

Cisplatin (CP), a common chemotherapy drug used in treatment of malignant tumors. Due to various side effects such as nephrotoxicity (kidney damage), it's efficiency and therapeutic application are limited. This study focuses on finding a suitable drug that would attenuate the side effects like kidney damage, caused by CP. Huaier polysaccharide (HP-1), an extraction of Trametes robiniophila Murr, with a molecular weight of 3 × 104 Da. Previous studies have shown that HP-1, exhibits anti-tumor potential and immunomodulatory effects. We hypothesized that HP-1 has the effect of attenuating the nephrotoxicity caused by CP chemotherapy and protecting renal function. Through our experiments, we observed that HP-1 can attenuate the level of oxidative stress, inflammation and mitochondrial dysfunction, thereby reducing kidney damage. In vitro, we observed that HP-1 significantly inhibits CP-induced renal tubular cell apoptosis and cell cycle arrest. In addition, HP-1 also affects the expression level of the protein by regulating the PI3K/Akt/mTOR signaling pathway and thus attenuates the side effects induced by cisplatin. Therefore, HP-1 may be a potential drug for preventing CP-induced renal damage. Unlabelled Image • Huaier polysaccharide could ameliorate CP-induced nephrotoxicity. • Huaier polysaccharide could anti-oxidative stress, anti-inflammatory, and anti-apoptosis responses. • Huaier polysaccharide attenuates CP-induced kidney damage via PI3K/AKT signaling. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01418130
Volume :
139
Database :
Academic Search Index
Journal :
International Journal of Biological Macromolecules
Publication Type :
Academic Journal
Accession number :
141606434
Full Text :
https://doi.org/10.1016/j.ijbiomac.2019.07.219