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灵芝多糖对HepG2细胞诱导的肝癌小鼠肠道菌群及其菌群代谢功能的调节作用
引用本文:于雷,孙超,张曼旭. 灵芝多糖对HepG2细胞诱导的肝癌小鼠肠道菌群及其菌群代谢功能的调节作用[J]. 实用肝脏病杂志, 2021, 24(4): 476-479. DOI: 10.3969/j.issn.1672-5069.2021.04.006
作者姓名:于雷  孙超  张曼旭
作者单位:101100 北京市通州区120紧急救援中心(于雷,孙超);包头医学院第二附属医院普通外科(张曼旭)
基金项目:*北京市自然科学基金资助项目(编号:20198485)
摘    要:目的 研究灵芝多糖对HepG2细胞诱导的肝癌小鼠肠道菌群及其菌群代谢功能的调节作用.方法 采用HepG2细胞构建肝癌小鼠模型,将21只造模成功的肝癌小鼠随机分为模型组、灵芝多糖(GLP)和益生菌处理组,每组7只,另选择正常小鼠7只作为对照组,给予药物处理组动物GLP或益生菌灌胃,另两组采用生理盐水灌胃,连续干预2 w....

关 键 词:肝细胞癌  灵芝多糖  肠道菌群  小鼠
收稿时间:2020-10-29

Regulation of intestinal floras and their metabolism functions by ganoderma lucidum plysaceharide in mice with HepG2 cell-induced implanted cancer
Yu Lei,Sun Chao,Zhang Manxu. Regulation of intestinal floras and their metabolism functions by ganoderma lucidum plysaceharide in mice with HepG2 cell-induced implanted cancer[J]. Journal of Clinical Hepatology, 2021, 24(4): 476-479. DOI: 10.3969/j.issn.1672-5069.2021.04.006
Authors:Yu Lei  Sun Chao  Zhang Manxu
Affiliation:120 Emergency Rescue Center, Tongzhou 101100,Beijing, China
Abstract:Objective The aim of this experimental study was to implore the regulation of intestinal floras and their metabolism functions by ganoderma lucidum plysaceharide (GLP) in mice with HepG2 cell-induced implanted cancer. Methods The subcutaneous cancer in mice was established by HepG2 cell implantation, and 21 mice with successful implanted cancer were randomly divided into model, GLP-intervened and probiotics-intervened groups, with 7 in each. 7 normal mice were selected as control. The GLP and probiotics were administered intragastrically, while normal saline were given by gavage in model and control for 2 weeks. The diversity of intestinal floras, and fatty acid metabolites were detected by microscopy and denaturing gradient gel electrophoresis (DGGE). Results The number of Bifidobacterium, Lactobacillus, Escherichia Coli and Enterococcus in model group were(2.3±0.5)×1010 CFU/g, (12.2±2.2)×109 CFU/g, (3.9±1.5)×107 CFU/g and(5.0±1.2)×1010 CFU/g, all significantly higher than [(0.94±0.18)×1010 CFU/g,(3.49±0.66)×109 CFU/g, (1.12±0.11)×107 CFU/g and (0.57±0.06)×1010 CFU/g, respectively,P<0.05] in the control,ylajj@163.com while they were(1.1±0.1)×1010 CFU/g, (6.5±1.1)×109 CFU/g, (1.8±0.2)×107 CFU/g and (1.5±0.1)×1010 CFU/g in GLP-intervened group (P<0.05); the abundance, the diversity index and uniformity of intestinal floras in GLP-intervened group were (7.2±1.1)S,(4.8±1.1)H and (1.0±0.2)E, all significantly higher than [(5.7±1.2)S, (3.4±0.5)H and (0.7±0.1)E, respectively, P<0.05] in the model; the intestinal flora acetic acid, propionic acid and n-butyric acid in GLP-intervened group were (37.9±3.3)mmol/L,(3.9±0.2)mmol/L and (2.3±0.3)mmol/L, all significantly higher than [(26.8±3.2)mmol/L,(1.8±0.4)mmol/L and (1.8±0.2)mmol/L, respectively, P<0.05], while the D-lactic acid was (0.2±0.0)g/L, much lower than (0.5±0.1)g/L in the model (P<0.05). Conclusion The imbalance of intestinal floras is closely related to the carcinogenesis in mice, and the GLP administration might correct the intestinal microecological disorders, which warrants further investigation.
Keywords:Hepatoma  Ganoderma lucidum plysaceharide  Intestinal flora  Mice  
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