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机构地区:[1]兰州大学校医院,兰州730000 [2]兰州大学中西医结合研究所,兰州730000
出 处:《中国实验方剂学杂志》2012年第3期150-152,共3页Chinese Journal of Experimental Traditional Medical Formulae
基 金:甘肃省自然科学研究基金计划项目(096RJZA060);兰州大学医学科研基金资助项目(LZUYX200805)
摘 要:目的:研究中药扶正解毒颗粒(FJG)对硫酸镍(NiSO4)染毒大鼠肾组织核因子-κB(NF-κB)活化的影响。方法:50只Wistar大鼠采用NiSO4 2.5 mg.kg-1 ip(连续7 d,此后间日1次)制备肾损伤模型,随机分为NiSO4组(模型组)、FJG高、中、低剂量组(分别为20,10,5 g.kg-1.d-1),二硫基丁二酸(DMSA),50 mg.kg-1.d-1)组。另设NS组(空白对照)及FJG对照组(FJG 10 g.kg-1.d-1)。各组大鼠ig 1次/d,共4周。测定各组大鼠血尿素氮(BUN)、肌酐(SCr)及24 h尿蛋白定量(24 h-UP),免疫组化SP法观察肾组织NF-κB活化。结果:NiSO4组大鼠出现肾功能损伤,NF-κB活化:肾小球(34.62±9.11)%,肾小管(62.45±14.78)%;FJG大剂量组NF-κB活化:肾小球(2.08±0.64)%,肾小管(11.48±3.39)%,明显低于NiSO4组(P<0.01),肾功能损伤亦明显减轻(P<0.05,P<0.01)。结论:FJG可能通过抑制肾组织NF-κB活性的异常升高而发挥拮抗镍性肾损伤的作用。Objective:To study the effects of Fuzheng Jiedu Granula(FJG) on the activation of nuclear factor-kappa-B(NF-κB) in rats exposed to nickel(nickel sulfate,NiSO4).Method: Rat nephrotoxicity model was established by intraperitoneal injection of NiSO4(2.5 mg·kg-1·d-1).They were randomized into 5 groups,model group,FJG high dose group(20 g·kg-1·d-1),FJG middle dose group(10 g·kg-1·d-1),FJG,low dose group(5 g·kg-1·d-1),meso-2,3-dimercaptosuccinic acid(DMSA) group(0.05 g·kg-1·d-1).Twenty Wistar rats were randomly divided into NS group and FJG control group(10 g·kg-1·d-1).Rats in each group were treated by intragastric administration once every day for four weeks.The levels of blood ureanitrogen(BUN),Creatinine(Scr) and 24 hours-proteinuria(24 h-UP) were measured.The activation of NF-κB was measured with immunohistochemistry methods.Result: In FJG groups,the levels of BUN,Scr,24h-UP and the activation of NF-κB were all decreased(P0.05,P0.01),compared with that of NiSO4 group.Conclusion: Inhibiting the activation of NF-κB,FJG could protect renal from injury induced by nickel.
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