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纸质出版日期:2012
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滕玉莲, 吕晓云, 赵健雄. 扶正解毒颗粒对染镍大鼠肾组织核因子-B活化的影响[J]. 中国实验方剂学杂志, 2012,18(3):150-152.
TENG Yu-lian, LV Xiao-yun, ZHAO Jian-xiong. Effects of Fuzheng Jiedu Granula on the Activation of NF-B in Rats Exposed to Nickel[J]. Chinese journal of experimental traditional medical formulae, 2012, 18(3): 150-152.
滕玉莲, 吕晓云, 赵健雄. 扶正解毒颗粒对染镍大鼠肾组织核因子-B活化的影响[J]. 中国实验方剂学杂志, 2012,18(3):150-152. DOI:
TENG Yu-lian, LV Xiao-yun, ZHAO Jian-xiong. Effects of Fuzheng Jiedu Granula on the Activation of NF-B in Rats Exposed to Nickel[J]. Chinese journal of experimental traditional medical formulae, 2012, 18(3): 150-152. DOI:
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(P<0.05
P<0.01)
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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