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餵食樟芝子實體對於小鼠體內肝腫瘤細胞之免疫調節與抑制腫瘤效果之探討

Immunomodulatory and Anti-tumor Effects of Oral Administration with Antrodia cinnamomea Fruiting Bodies in BALB/c Mice

摘要


The objective of this study was to investigate the immunomodulatory and anti-tumor effects of Antrodia cinnamomea fruiting bodies using a hepatoma-bearing mouse model. Oral administration of high (100 mg/kg B.W.) and medium (33 mg/kg B.W.) doses of A. cinnamomea fruiting bodies significantly increased the life spun of ATCC BNL IMEA.7R.1 hepatoma-bearing mice (3×10^2 cells/mouse) by 47.4 and 57.1%, respectively. In naive (un-injected with tumor cells) mice, orally administered A. cinnamomea fruiting bodies at high, medium, and low (11 mg/kg B. W.) doses significantly enhanced the production of TNF-α by peritoneal macrophages (p<0.05). Oral administration of A. cinnamomea fruiting bodies at medium and low doses also significantly enhanced the production of nitric oxide by peritoneal macrophages (p<0.05). In addition, peritoneal macrophages obtained from A. cinnamomea fruiting bodies-fed naive mice had increased cytotoxicity against hepatoma cells. In hepatoma-bearing mice, oral administration of A. cinnamomea fruiting bodies significantly increased the serum levels of tumor-specific IgG (p<0.05). Splenocytes obtained from A. cinnanmomea fruiting bodies-fed heputoma-bearing mice had increased tumor-specific proliferation and upregulated production of IFN-γ, IL-2, and TNF-α, as well as enhanced cytotoxicity against hepatoma cells, These results indicated that A. cinnamomea fruiting bodies carried out anti-tumor activity by activating both non-specific and tumor-specific immunity.

並列摘要


The objective of this study was to investigate the immunomodulatory and anti-tumor effects of Antrodia cinnamomea fruiting bodies using a hepatoma-bearing mouse model. Oral administration of high (100 mg/kg B.W.) and medium (33 mg/kg B.W.) doses of A. cinnamomea fruiting bodies significantly increased the life spun of ATCC BNL IMEA.7R.1 hepatoma-bearing mice (3×10^2 cells/mouse) by 47.4 and 57.1%, respectively. In naive (un-injected with tumor cells) mice, orally administered A. cinnamomea fruiting bodies at high, medium, and low (11 mg/kg B. W.) doses significantly enhanced the production of TNF-α by peritoneal macrophages (p<0.05). Oral administration of A. cinnamomea fruiting bodies at medium and low doses also significantly enhanced the production of nitric oxide by peritoneal macrophages (p<0.05). In addition, peritoneal macrophages obtained from A. cinnamomea fruiting bodies-fed naive mice had increased cytotoxicity against hepatoma cells. In hepatoma-bearing mice, oral administration of A. cinnamomea fruiting bodies significantly increased the serum levels of tumor-specific IgG (p<0.05). Splenocytes obtained from A. cinnanmomea fruiting bodies-fed heputoma-bearing mice had increased tumor-specific proliferation and upregulated production of IFN-γ, IL-2, and TNF-α, as well as enhanced cytotoxicity against hepatoma cells, These results indicated that A. cinnamomea fruiting bodies carried out anti-tumor activity by activating both non-specific and tumor-specific immunity.

被引用紀錄


潘日鴻(2009)。大型樟芝發酵液對肝癌細胞Hep G2生長抑制之探討〔博士論文,國立臺灣大學〕。華藝線上圖書館。https://doi.org/10.6342/NTU.2009.02229

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