[Effect of Ganoderma lucidum polysaccharides on intestinal mucosal immune system in H22 liver cancer bearing mice]

Zhongguo Zhong Xi Yi Jie He Za Zhi. 2009 Apr;29(4):335-9.
[Article in Chinese]

Abstract

Objective: To observe the mucosal immune mechanism of anti-tumor action of Ganoderma lucidum polysaccharides (GLP).

Methods: The concentration of H22 cells in suspension were adjusted to 1 x 10(9)/ L, and 0.2 mL of the cell suspension was injected subcutaneously in the right oxter of Kunming mice. Then the H22 bearing mice were randomly divided into 4 groups: the GLP group, the Cytoxan (CTX) group, the CTX + GLP group and the untreated model group, 8 mice in each group. Besides, a blank control group was set up. Starting from the 2nd day of modeling, GLP, at the dose of 1.02 g/kg was given to GLP group and GLP + CTX group by gastrogavage once a day for 12 successive days; CTX at the dose of 100 mg/kg was administered via peritoneal injection to the CTX group and the GLP + CTX group on the 1st day and the 6th day of the experimental course; but to the model group and the blank group, only equal volume of distilled water was given. All mice were sacrificed on the 14th day, the ileum at 1 cm upper to cecum was taken, through 4% paraform fixation and paraffin section, it was used for immunohistochemical detecting expressions of immunoglobulin A (IgA), tumor necrosis factor-alpha (TNF-alpha), interleukin-2 (IL-2) and interleukin-10 (IL-10) in ileum. Besides, the lymphocyte subsets in the intraepithelial lymphocyte (IEL), lamina propria lymphocytes (LPL), and Peyer's patch lymphocytes (PPL) were analyzed by immune fluorescence technique and flow cytometry.

Results: Compared with the blank control group, the phenotype of lymphocytes and the expression of cytokines in ileum in the model group changed significantly; and the phenotype was variant in different regions. Compared with the model group, both indexes were adjusted in the GLP, CTX and GLP + CTX group to different degrees.

Conclusion: The adjustment of GLP on intestinal mucosal immune is probably another path for its anti-tumor action.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antineoplastic Agents, Phytogenic / pharmacology*
  • Drugs, Chinese Herbal / pharmacology
  • Immunoglobulin A / metabolism
  • Interleukin-2 / metabolism
  • Intestinal Mucosa / immunology*
  • Liver Neoplasms, Experimental / immunology*
  • Male
  • Mice
  • Mice, Inbred Strains
  • Polysaccharides / isolation & purification
  • Polysaccharides / pharmacology*
  • Random Allocation
  • Reishi / chemistry*
  • Tumor Necrosis Factor-alpha / metabolism

Substances

  • Antineoplastic Agents, Phytogenic
  • Drugs, Chinese Herbal
  • Immunoglobulin A
  • Interleukin-2
  • Polysaccharides
  • Tumor Necrosis Factor-alpha