The influence of active hexose correlated compound (AHCC) on cisplatin-evoked chemotherapeutic and side effects in tumor-bearing mice

被引:33
作者
Hirose, Aya
Sato, Eri
Fujii, Hajime
Sun, Buxiang
Nishioka, Hiroshi
Aruoma, Okezie I.
机构
[1] Touro Coll Pharm, Dept Pharmaceut & Biomed Sci, New York, NY 10027 USA
[2] Amino Up Chem Co, Kiyota Ku, Sapporo, Hokkaido 0040839, Japan
关键词
active hexose correlated compounds (AHCC); cisplatin; cis-diaminedichloroplatinum (II); anticancer drugs; cancer chemotherapy-side effects; nephrotoxicity; chernoprevention strategies; kidney failure; chronic inflammation; redox biochemistry; economics of cancer therapy; complementary medicine;
D O I
10.1016/j.taap.2007.03.031
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cisplatin (cis-diaminedichloroplatinum (11) or CDDP) (a widely used platinum-containing anticancer drug) is nephrotoxic and has a low percentage of tolerance in patients during chemotherapy. The active hexose correlated compound (AHCC) is an extract of Basidiomycotina marketed as a supplement for cancer patients due to its nutrients and fibre content and its ability to strengthen and optimize the capacity of the immune system. The possibility that AHCC could reduce the side effects of cisplatin was assessed in the tumor-bearing BALB/cA mice on the basis of the ability to ameliorate the cisplatin-induced body weight loss, anorexia, nephrotoxicity and hematopoietic toxicity. Although cisplatin (8 mg/kg body weight) reduced the size and weight of the solid tumors, supplementation with AHCC significantly enhanced cisplatin-induced antitumor effect in both the size (p<0.05) and weight (p<0.05). Food intake in the cisplatin-treated mice were decreased following commencement of treatment and this remained low compared with the cisplatin-untreated group (control) throughout the experiment period. Supplementation with AHCC increased the food intake in the cisplatin-treated mice. The blood urea nitrogen and serum creatinine concentrations, and the ratio of blood urea nitrogen to serum creatinine were significantly increased in the cisplatin alone treated group compared to the control group. Their increased levels were mitigated by supplementation with AHCC (100 mg/kg body weight) in the cisplatin-treated group. AHCC was also able to modulate the suppression of bone marrow due to cisplatin and the improvement was statistically significant. The histopathological examination of the kidney revealed the presence of cisplatin-induced damage and this was modulated by AHCC treatment. The potential for AHCC to ameliorate the cisplatin-evoked toxicity as well as the chemotherapeutic effect could have beneficial economic implications for patients undergoing chemotherapy with cisplatin. (C) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:152 / 158
页数:7
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