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作 者:潘华新[1] 王丽虹[1] 罗霞[1] 周联[1] 王青[1] 邓向亮[1]
机构地区:[1]广州中医药大学,广州510405
出 处:《中药新药与临床药理》2012年第4期438-440,496,共4页Traditional Chinese Drug Research and Clinical Pharmacology
基 金:广东省自然科学基金资助项目(10151040701000054);广东省教育部产学研结合项目(2010A090200041)
摘 要:目的研究四君子汤总多糖(SJZPS)对化疗荷瘤小鼠脾脏、派氏结(PPs)、肠系膜淋巴结(MLNs)淋巴细胞的影响。方法将BALB/c小鼠随机分为对照组、肿瘤模型组,环磷酰胺(CY)化疗组和四君子汤总多糖治疗(CY+SJZPS)组。CY组和CY+SJZPS组每天腹腔注射CY20 mg.kg-1,CY+SJZPS组同时灌胃SJZPS 1g.kg-1,连续给药9 d。应用流式细胞术检测脾脏、小肠PPs和MLNs中T、B淋巴细胞比例、活化水平以及T细胞亚群的变化。结果 SJZPS能提高肠道PPs中B淋巴细胞的比例和活化水平,降低MLNs中CD4+/CD8+的比值,改善化疗所致的肠道黏膜免疫损伤;SJZPS能提高化疗荷瘤小鼠脾脏淋巴细胞中B淋巴细胞的比例,及T、B淋巴细胞的活化水平,同时降低CD4+/CD8+的比值以改善化疗荷瘤小鼠系统免疫功能,其中SJZPS对B细胞的作用更加明显。结论 SJZPS能有效拮抗化疗药物所致的小鼠肠黏膜免疫功能损伤,同时对整体免疫功能具有改善作用。Objective To explore the effects of polysaccharides of Sijunzi decoction(SJZPS) on lymphocyte in spleen, Peyer's patchs(PPs) and mesenteric lymph nodes(MLNs) in tumor-bearing mice tread with chemotherapy. Methods BALB/c mice were randomly divided into four groups, control group, tumor model group, cyclophosphamide (CY) chemotherapy group and SJZPS treatment(CY+SJZPS) group. CY group and CY+SJZPS group daily intraperitoneal in- jection administration of eyelophosphamide(20 mg·kg^-1), CY+SJZPS group daily oral administration of SJZPS(1 g·kg^-1) at the same time. The proportion and activation level of (T, B) lymphocyte, subsets of T lymphocyte isolated from spleen, PPs and MLNs were detected by flow cytometer. Results In CY+SJZPS group, the intestine mucosal im- munity injury induced by cyclophosphamide was improved by increasing the proportion and activation level of B lym- phocyte in PPs, decreasing the ratio of CD4^+/CD8^+ in MLNs, and the systematic immunity was improved by increasing the proportion of B cell and the activation level of T, B cell, and decreasing the ratio of CD4^+/CD8^+ of spleen lympho- cyte in tumor-bearing mice tread with chemotherapy. Conclusion Polysaceharides of Sijunzi decoction can effectively antagonize the injury on intestine mucosal immunity induced by eyclophosphamide in tumor-bearing mice, and can im- prove the systematic immunity.
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