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大黄蒽醌提取物缓解小鼠肾组织纤维化作用的实验研究 被引量:8

Administration of Rhubarb extract attenuates renal fibrosis in mice
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摘要 目的通过观察大黄蒽醌提取物抑制小鼠病变肾组织纤维化的作用,探讨大黄治疗肾脏病的作用机制。方法采用左侧输尿管结扎的方法建立单侧输尿管梗阻(UUO)雄性CD-1 小鼠动物模型。用形态学半定量方法评价组织学病变;酸水解-比色法测定肾组织胶原的含量; 蛋白印迹技术检测胶原α表达的水平。以α-平滑肌肌动蛋白(α-SMA)作为上皮细胞转分化的观察指标。结果大黄提取物(50 mg/kg体重)能够显著地减少肾间质的病变,降低肾组织中胶原的聚积,与对照组相比两者差异均有统计学意义。大黄提取物(25、50 mg/kg体重)能够降低病变肾组织中胶原α的表达水平及减少梗阻肾组织中α-SMA的表达,抑制上皮细胞转分化。结论大黄蒽醌化合物能够改善肾脏的纤维化,其作用可能与降低肾组织内胶原的沉积以及抑制上皮细胞转分化有关。 Objective To investigate the mechanism of Rhubarb in treating chronic kidney disease. Methods The animal model of renal disease was induced by unilateral ureteral obstruction (UUO) in CD-1 mice. The mice were divided into three groups: the sham, UUO, and UUO receiving Rhubarb extract treatment (12.5, 25, and 50 mg/kg body weight) daily. The morphological changes and content of total collagen from each group were examined at day 7 following UUO. Meanwhile, the de novo expression of a-smooth muscle actin (α-SMA), and collagen Ⅰ in tissues from mice were assessed by Western blotting. Results Administration of Rhubarb extract markedly attenuated renal tissue injury, and decreased total collagen accumulation. The expression of α-SMA was suppressed dramatically in the mice receiving Rhubarb extract treatment (50 mg/kg body weight). In addition, Rhubarb extract inhibited deposition of collagen Ⅰ significantly. Conclusion Rhubarb extract is a drug for amehoration of renal fibrosis of mice in vivo.
出处 《中华肾脏病杂志》 CAS CSCD 北大核心 2006年第6期360-363,共4页 Chinese Journal of Nephrology
基金 国家自然科学基金(30270616 304708005)江苏省自然科学基金(BK2004160)南京医科大学第一附属医院回国人员科研启动基金
关键词 大黄属 纤维化 胶原 Α-平滑肌肌动蛋白 Rhubarb Fibrosis Collagen α-Smooth muscle actin
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  • 1李莉,黎磊石.1001例原发性肾小球肾炎病理学类型分布及临床特点[J].中华医学杂志,1989,69(1):20-23. 被引量:12
  • 2陈惠萍,黎磊石.脂蛋白肾小球病[J].肾脏病与透析肾移植杂志,1997,6(2):182-184. 被引量:20
  • 3杨俊伟,中华内分泌代谢杂志,1993年,9卷,217页
  • 4杨俊伟,中华肾脏病杂志,1993年,9卷,65页
  • 5刘志红,肾脏病与透析肾移植杂志,1992年,1卷,103页
  • 6Eddy AA. Molecular basis of renal fibrosis. Pediatr Nephrol,2000, 15:290-301.
  • 7Muller GA, Zeisberg M, Strutz F. The importance of tubulointerstitial damage in progressive renal disease. Nephrol Dial Transplant, 2000,15: 76-77.
  • 8Massague J. How cells read TGF-beta signals. Nat Rev Mol Cell Biol, 2000,1 : 169-178.
  • 9Border WA, Noble NA. TGF-beta in kidney fibrosis: a target for gene therapy. Kidney Int, 1997, 51:1388-1396.
  • 10Yang JW, Dai CS, Liu YH. A novel mechanism by which hepatocyte growth factor blocks tubular epithelial to mesenchymal transition. J Am Soc Nephrol, 2005, 16: 68-78.

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