Maitake β-glucan enhances therapeutic effect and reduces myelosupression and nephrotoxicity of cisplatin in mice

被引:69
作者
Masuda, Yuki [1 ]
Inoue, Munechika [1 ]
Miyata, Ayu [1 ]
Mizuno, Shigeto [2 ]
Nanba, Hiroaki [1 ]
机构
[1] Kobe Pharmaceut Univ, Dept Microbial Chem, Higashinada Ku, Kobe, Hyogo 6588558, Japan
[2] Kobe Pharmaceut Univ, Dept Med Pharmaceut, Kobe, Hyogo 6588558, Japan
关键词
Grifola frondosa; beta-glucan; Cisplatin; Antitumor activity; Nephrotoxicity; Myelotoxicity; ACUTE-RENAL-FAILURE; COLONY-STIMULATING FACTOR; TUMOR-BEARING MICE; GRIFOLA-FRONDOSA; D-FRACTION; MD-FRACTION; IN-VITRO; NK CELLS; G-CSF; POLYSACCHARIDE;
D O I
10.1016/j.intimp.2009.02.005
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Cisplatin is broadly used clinically as an anticancer drug. Despite its significant anticancer activity, cisplatin-induced nephrotoxicity and myelosuppression limit its use. MD-Fraction is glucan purified from maitake (Grifola frondosa), which has beta-1, 6-main chain with beta-1, 3-branches, has been reported to exhibit antitumor and antimetastatic activities by enhancing the immune system. In this study, we demonstrate that MD-Fraction in combination with cisplatin significantly enhanced antitumor and antimetastatic activity compared to cisplatin alone. MD-Fraction reduced decreases in body weight, spleen weight and the number of immunocompetent cells such as macrophages, DCs and NK cells in cisplatin-treated mice. MD-Fraction also induced IL-12p70 production by splenocytes, resulting in increased NK cell activity in cisplatin-treated mice. MD-Fraction significantly increased the mRNA expression of GM-CSF, G-CSF, M-CSF, IFN-gamma, IL-12 p40 in splenocytes and reduced the decrease in the number of CFU-GM colonies in cisplatin-treated bone marrow. These facts suggest that MD-Fraction can reduce cisplatin-induced myelosuppression. Moreover, treatment with MD-Fraction significantly reduced cisplatin-induced nephrotoxicity accompanied by increases in serum creatinine level, necrosis and apoptosis of renal tubular cells. These results suggest that MD-Fraction in combination with cisplatin cannot only enhance antitumor and antimentastatic acitivity, but also reduce cisplatin-induced myelotoxicity and nephrotoxicity. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:620 / 626
页数:7
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