Molecular mechanism underlying chemoprotective effects of Ganoderma atrurn polysaccharide in cyclophosphamide-induced immunosuppressed mice

被引:56
|
作者
Yu, Qiang [1 ]
Nie, Shao-Ping [1 ]
Wang, Jun-Qiao [1 ]
Huang, Dan-Fei [1 ]
Li, Wen-Juan [1 ]
Xie, Ming-Yong [1 ]
机构
[1] Nanchang Univ, State Key Lab Food Sci & Technol, Nanchang 330047, Peoples R China
基金
中国国家自然科学基金;
关键词
Ganoderma atrum polysaccharide; Cyclophosphamide; Peritoneal macrophages; Spleen lymphocytes; Immunosuppression; FACTOR-ALPHA SECRETION; PROTEIN-KINASE-C; STRUCTURAL-CHARACTERIZATION; IMMUNOMODULATORY ACTIVITY; MACROPHAGE ACTIVATION; LYMPHOCYTE-ACTIVATION; SIGNALING PATHWAY; FRUITING BODIES; KAPPA-B; ANTIOXIDANT;
D O I
10.1016/j.jff.2015.03.015
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
The molecular mechanism underlying the chemoprotective effects of Ganoderrna atrum polysaccharide in cyclophosphamide-induced immunosuppressed mice was investigated. In Cy-treated mice, PSG-1 treatment significantly promoted the phagocytosis, and stimulated the production of NO and cytokines (TNF-alpha and IL-1 beta) in peritoneal macrophages. Moreover, PSG-1 elevated the phosphorylation of MAPKs and Akt, as well as expression of NP-kappa B in peritoneal macrophages. In addition, PSG-1 enhanced the recovery of T and B cell proliferation responses in Cy-treated mice. Furthermore, Ca2+ concentration and PKC activity of spleen lymphocytes in PSG-1 groups dramatically increased as compared with that of the model group. Finally, PSG-1 administration was found to dose-dependently improve the decline of cAMP level and PICA activity caused by Cy. These findings indicated that the chemoprotective effects of PSG-1 may be attributed to its capacity to activate peritoneal macrophages and spleen lymphocytes in Cy-treated mice. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:52 / 60
页数:9
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