鞠佃文, 郑钦岳, 曹雪涛, 梅小斌, 易杨华. 商陆皂苷甲对大鼠Heymann肾炎的治疗作用及对细胞因子的影响J. 药学学报, 1999, 34(1): 9-9.
引用本文: 鞠佃文, 郑钦岳, 曹雪涛, 梅小斌, 易杨华. 商陆皂苷甲对大鼠Heymann肾炎的治疗作用及对细胞因子的影响J. 药学学报, 1999, 34(1): 9-9.
Ju Dianwen, Zheng Qinyue, Cao Xuetao, Mei Xiaobin , Yi Yanghua, . THERAPEUTIC EFFECTS OF ESCULENTOSIDE A ON PASSIVE HEYMANN NEPHRITIS IN RATS AND ITS INHIBITION ON CYTOKINE PRODUCTIONJ. Acta Pharmaceutica Sinica, 1999, 34(1): 9-9.
Citation: Ju Dianwen, Zheng Qinyue, Cao Xuetao, Mei Xiaobin , Yi Yanghua, . THERAPEUTIC EFFECTS OF ESCULENTOSIDE A ON PASSIVE HEYMANN NEPHRITIS IN RATS AND ITS INHIBITION ON CYTOKINE PRODUCTIONJ. Acta Pharmaceutica Sinica, 1999, 34(1): 9-9.

商陆皂苷甲对大鼠Heymann肾炎的治疗作用及对细胞因子的影响

THERAPEUTIC EFFECTS OF ESCULENTOSIDE A ON PASSIVE HEYMANN NEPHRITIS IN RATS AND ITS INHIBITION ON CYTOKINE PRODUCTION

  • 摘要: 目的: 商陆皂苷甲(EsA)对大鼠Heymann肾炎(passive Heymann nephritis,PHN)的治疗作用及机理。方法: 大鼠sc Fx1A抗原的抗体制成自身免疫性肾小球肾炎,EsA 5,10和20 mg.kg-1.d-1 ip,连续14 d。结果: EsA可以显著减少肾炎大鼠尿蛋白的产生,电镜和免疫荧光检查发现EsA治疗后肾炎大鼠病理情况明显好转。EsA治疗对血清中炎性细胞因子肿瘤坏死因子(TNF)、白细胞介素1(IL-1)和白细胞介素6(IL-6)的产生具有显著的抑制作用。结论: EsA对大鼠Heymann肾炎具有显著治疗作用,抑制细胞因子产生可能参与EsA抗炎机制。

     

    Abstract: AIM: To investigate the therapeutic effects of esculentoside A, a kind of saponin isolated from the root of the Chinese herb Phytolaca esculenta, on passive Heymann nephritis (PHN) in rats. METHODS: PHN was prepared by injecting Fx1A antibody in rats, and esculentoside A 5, 10 and 20 mg.kg-1 were administered intraperitonealy once a day for 14 consecutive days for the treatment of PHN rats. RESULTS: Esculentoside A 5, 10 and 20 mg.kg-1 decreased urine protein production significantly. Pathological analysis revealed that deposits of IgG along the capillary wall of the glomerulus, glomerulus base membrane thickness and electron-dense deposits in PHN rats after treatment with esculentoside A were less than those in control rats. Decreased levels of TNF, IL-1 and IL-6 were observed in the sera of PHN rats following esculentoside A administration. TNF, IL-1 and IL-6 are important cytokines involved in the pathogenesis of inflammatory lesions. CONCLUSION: Esculentoside A possessed potent anti-inflammatory effects on PHN. Inhibition of inflammatory cytokine production may partially explain the anti-inflammatory effects of esculentoside A.

     

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