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Effects of the polysaccharides extracted from Ganoderma lucidum on chemotherapy-related fatigue in mice.

Authors :
Ouyang, Ming-zi
Lin, Li-zhu
Lv, Wen-jiao
Zuo, Qian
Lv, Zhuo
Guan, Jie-shan
Wang, Shu-tang
Sun, Ling-ling
Chen, Han-rui
Xiao, Zhi-wei
Source :
International Journal of Biological Macromolecules. Oct2016, Vol. 91, p905-910. 6p.
Publication Year :
2016

Abstract

The weight-loaded swimming capability, tumor growth, survival time and biochemical markers of Ganoderma lucidum polysaccharides (GLPs) in a chemotherapy-related fatigue mouse model were tested in the present study. The results showed that the middle-dose GLPs (GLP-M) and the high-dose GLPs (GLP-H) could increase the exhausting swimming time, which was observed to decrease in the cisplatin control group(PCG) and the tumor control group (TCG).The GLP-M and the GLP-H had reduced serum levels of tumor necrosis factor-αand interleukin-6, which were up-regulated by cisplatin. Cisplatin and the presence of tumor significantly enhanced the malondialdehyde (MDA) content and inhibited the activity of superoxide dismutase (SOD) in the muscle. Administration of GLPs at a high dose decreased the levels of MDA and up-regulated the SOD activity. The high-dose GLPs + cisplatin group presented a decreased tendency of tumor volume and a lower tumor weight compared with PCG. Moreover, the mice in the GLP-M and GLP-H groups had longer survival times compared with the mice in the TCG and PCG.The levels of creatinine and serum blood urea nitrogen, which are up-regulated by cisplatin, were significantly reduced by GLP-M and GLP-H. Therefore, these results suggest that GLPs might improve chemotherapy-related fatigue via regulation of inflammatory responses, oxidative stress and reduction of nephrotoxicity. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
01418130
Volume :
91
Database :
Academic Search Index
Journal :
International Journal of Biological Macromolecules
Publication Type :
Academic Journal
Accession number :
117335935
Full Text :
https://doi.org/10.1016/j.ijbiomac.2016.04.084