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时间:2020-05-08
《壮肾排毒方抗肾纤维化的机制研究-论文.pdf》由会员上传分享,免费在线阅读,更多相关内容在行业资料-天天文库。
1、实用中医药杂志2014年3.hJ~3og3期(总第254期)JOURNALOFPRACTICALTRADITIONALCHINESEMEDICINE2014.Vo1.3ON0-3壮肾排毒方抗肾纤维化的机制研究刘立昌2刘新,刘旭生。,杜雪飞,冯敏坚。,张玉婷。,洪伟洪,王利纯(1.广州中医药大学2011~博士研究生,广东广州510405;2.广东省中医院珠海医院,广东珠海519015;3.广东省中医院,广东广州510120)[中图分类号]R289.592.9[文献标识码]B[文章编号]1004—2814(2014)03—0174—02[摘要]目的:探讨壮肾排毒方抗肾纤维化的作用机制,为临床应用
2、提供实验依据。方法:48只雄性Wistar大鼠随机分为正常组、模型组、壮肾排毒方组、福辛普利组各12只。除正常组外其余各组均行5/6肾切除手术制作慢性肾衰竭(CRF)动物模型。于造模第2次手术后1周开始干预,干预12周后取血清及肾组织标本,全自动生化分析仪检测血清尿素氮(BUN)、血肌酐(Scr)。免疫组织化学方法检测肾组织血肿瘤坏死因子一o【(TNF—)、转化生长因子一B(TGF—B)的表达。结果:模型组、壮肾排毒方组、福辛普利组大鼠血清BUN、Scr肾脏组织TNF-o【、TGF—B与正常组比较有显著性差异(P3、壮肾排毒方组、福辛普利组比较有显著性差异(P4、dencesforclinicalapplication.Methods:48Wistarmaleratsweredividedintofourgroupsrandomly,namelynormalcontrolgroup(sham—operationgroup,12rats),modelgroup(12rats),ZhuangshenPaidugroup(12rats)andFosinoprilgroup(12cases).Excepttheratsinsham—operationgroup,CRFmodelswerepreparedwith5/6nephrectomyintherestg5、roups.Interventionstartedlwafterthesecondoperationofmodeling.12wafterintervention,serumandkidneytissuespecimenwerecollected.AutomaticbiochemistryanalyzerwasappliedforthedeterminationofBUNandScr.ImmunohistochemistrywasforthetestoftheexpressionofTNF-otandTGF一131inkidneytissue.Results:Thesignificantdi6、ferencewaspresentedinserumBUNandScr,TNF—otandTGF-p1inkidneytissueincomparisonofmodel,ZhuangshenPaidugroupandFosinoprilgroupwithsham-operationgroup(P7、antly(P<0.01,P
3、壮肾排毒方组、福辛普利组比较有显著性差异(P4、dencesforclinicalapplication.Methods:48Wistarmaleratsweredividedintofourgroupsrandomly,namelynormalcontrolgroup(sham—operationgroup,12rats),modelgroup(12rats),ZhuangshenPaidugroup(12rats)andFosinoprilgroup(12cases).Excepttheratsinsham—operationgroup,CRFmodelswerepreparedwith5/6nephrectomyintherestg5、roups.Interventionstartedlwafterthesecondoperationofmodeling.12wafterintervention,serumandkidneytissuespecimenwerecollected.AutomaticbiochemistryanalyzerwasappliedforthedeterminationofBUNandScr.ImmunohistochemistrywasforthetestoftheexpressionofTNF-otandTGF一131inkidneytissue.Results:Thesignificantdi6、ferencewaspresentedinserumBUNandScr,TNF—otandTGF-p1inkidneytissueincomparisonofmodel,ZhuangshenPaidugroupandFosinoprilgroupwithsham-operationgroup(P7、antly(P<0.01,P
4、dencesforclinicalapplication.Methods:48Wistarmaleratsweredividedintofourgroupsrandomly,namelynormalcontrolgroup(sham—operationgroup,12rats),modelgroup(12rats),ZhuangshenPaidugroup(12rats)andFosinoprilgroup(12cases).Excepttheratsinsham—operationgroup,CRFmodelswerepreparedwith5/6nephrectomyintherestg
5、roups.Interventionstartedlwafterthesecondoperationofmodeling.12wafterintervention,serumandkidneytissuespecimenwerecollected.AutomaticbiochemistryanalyzerwasappliedforthedeterminationofBUNandScr.ImmunohistochemistrywasforthetestoftheexpressionofTNF-otandTGF一131inkidneytissue.Results:Thesignificantdi
6、ferencewaspresentedinserumBUNandScr,TNF—otandTGF-p1inkidneytissueincomparisonofmodel,ZhuangshenPaidugroupandFosinoprilgroupwithsham-operationgroup(P7、antly(P<0.01,P
7、antly(P<0.01,P
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