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百令对慢性肾衰竭大鼠模型肾纤维化治疗机制研究
引用本文:郭敏,杜跃亮,郭伟杰. 百令对慢性肾衰竭大鼠模型肾纤维化治疗机制研究[J]. 实用诊断与治疗杂志, 2014, 0(3): 229-231
作者姓名:郭敏  杜跃亮  郭伟杰
作者单位:漯河市中心医院漯河医学高等专科学校第一附属医院肾内科,河南漯河462000
摘    要:目的观察百令对慢性肾衰竭大鼠模型24h尿蛋白定量、血肌酐、肾脏组织病理及细胞因子表达的影响,探讨其对肾纤维化的治疗作用。方法80只SD大鼠随机分为假手术组(20只)和手术组(60只),手术组行5/6。肾切除术,模型制作成功后分为手术未治疗组15只、百令低剂量组(1.0g/(kg·d))15只、百令中剂量组(2.0g/(kg·d))15只和百令高剂量组(3.og/(kg·d))15只。假手术组随机分为假手术组未治疗组10只和假手术百令组(2.0g/(kg·d))10只。假手术百令组和百令低、中、高剂量组于手术4周后开始给药,每日灌胃,假手术组未治疗组、手术未治疗组每日生理盐水灌胃。治疗4周后检测24h尿蛋白定量、血肌酐,取残肾检测肾小球系膜基质面积/肾小球囊面积及肾小管-间质损伤指数,免疫组织化学法检测肾组织转化生长因子-β1表达。结果手术组24h尿蛋白定量、血肌酐、肾小球系膜基质面积/肾小球囊面积及肾小管-间质损伤指数、肾组织表达转化生长因子-β1较假手术组升高(P〈0.01),百令各治疗组上述指标较手术未治疗组下降(P〈0.01),百令高剂量组较中、低剂量组上述指标下降,两两比较差异均有统计学意义(P〈0.01)。结论百令可保护残肾功能,通过下调转化生长因子-β1表达延缓肾纤维化进展。

关 键 词:慢性肾衰竭  肾纤维化  大鼠  百令  转化生长因子-β1

Therapeutic effect of Bailing on renal fibrosis in rat models with chronic renal failure
GUO Min,DU Yue-liang,GUO Wei-jie. Therapeutic effect of Bailing on renal fibrosis in rat models with chronic renal failure[J]. Journal of Practical Diagnosis and Therapy, 2014, 0(3): 229-231
Authors:GUO Min  DU Yue-liang  GUO Wei-jie
Affiliation:(Department of Nephrology , Luohe Central Hospital, the First Affiliated Hospital of Luohe Medical College, Luohe 462000, China)
Abstract:Objective To explore the therapeutic effect of Bailing on renal fibrosis by observing 24-hour urinary protein excretion, serum creatinine, histopathologic features and cytokine expression in rat models with chronic renal failure. Methods Eighty SD rats were randomly divided into sham operation group (n = 20) and operation group (n = 60). Operation group underwent 5/6 nephrectomy to establish rat models and was redivided into operation untreated group, low-dose Bailing group (1. 0 g/(kg·d)), medium-dose Bailing group (2. 0 g/(kg · d)) and high-dose Bailing group (3.0 g/(kg· d)), with 15 rats in each group. Sham operation group was randomly redivided into sham operation untreated group and sham Bailing group (2.0 g/(kg · d)), with 10 rats in each group. Bailing groups received lavage with Bailing everyday 4 weeks after operation. Untreated groups received lavage with normal saline. The 24-hour urinary protein excretion and serum creatinine were detected. Mesangial matrix area/glomerular capsule area and renal tubule- mesenchymal injury indexes were measured. The expression of transforming growth factor-β1 (TGF-β1) was determined by immunohistochemical method. Results The 24-hour urinary protein excretion, serum creatinine, mesangial matrix area/glomerular capsule area, renal tubule-mesenchymal injury index and TGF-β1 were significantly higher in operation group than those in sham operation group (P〈0.01), were lower in Bailing groups than those in operation untreated group (P〈0.01), and were lower in high-dose Bailing group than those in medium- and low-dose Bailing groups, showing significant differences in multiple comparison (P〈0.01). Conclusions Bailing could protect the remnant kidney function and postpone renal fibrosis by decreasing the expression of TGF-β1 in renal tissues.
Keywords:Chronic renal failure  tubulointerstitial fibrosis  rat  Bailing  transforming growth factor-β1
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