摘要
目的:研究中药复方地灵丹汤对单侧输尿管梗阻(unilateral ureteral obstruction,UUO)致肾间质纤维化模型大鼠肾间质纤维化的防治作用及其可能机制。方法:将60只SD大鼠随机分为假手术组、模型组、依那普利组及地灵丹组。采用UUO法建立肾间质纤维化大鼠模型,观察血尿素氮、血清肌酐和24h尿蛋白定量及肾组织病理改变,并采用免疫组织化学法检测转化生长因子β1(transforming growth factor-β1,TGF-β1)、α-平滑肌肌动蛋白(α-smooth muscle actin,α-SMA)、纤维连接蛋白(fibronectin,FN)及层黏连蛋白(laminin,LN)的表达。结果:第7天模型组肾间质大量炎症细胞浸润及胶原表达,TGF-β1、FN和LN表达面积百分率较假手术组明显增加(P<0.05);地灵丹组间质纤维化面积较模型组减少(P<0.05)。第14天地灵丹组和依那普利组肾间质TGF-β1、α-SMA、FN和LN表达面积百分率较模型组减少(P<0.05),BUN、SCr和24h尿蛋白无明显差异。第21天地灵丹组SCr、肾间质纤维化和TGF-β1表达面积百分率较依那普利组和模型组下降(P<0.05)。结论:地灵丹能减轻单侧输尿管梗阻模型大鼠的蛋白尿和肾间质纤维化,抑制TGF-β1、α-SMA、FN和LN的表达。在较长时间应用后,地灵丹对模型大鼠的肾功能保护作用优于依那普利。
Objective: To investigate the preventive and therapeutic effects and the possible mechanisms of Dilingdan Decoction (DLDD), a compound Chinese herbal medicine, on rats with renal tubulointerstitial fibrosis induced by unilateral ureteral obstruction (UUO).
Methods: Sixty SD rats were randomly divided into sham-operated group, untreated group, enalapril-treated group and DLDD-treated group. Blood urea nitrogen (BUN), serum creatinine (SCr), urine protein quantization in 24 hours and pathological changes of the obstructed kidney were observed. The expressions of transforming growth factor-β1 (TGF-β1), alpha-smooth muscle actin (α-SMA), fibronectin (FN) and laminin (LN) were detected by immunohistochemical method and colored-multimedia pathological image analysis system.
Results: Massive inflammatory infiltrates and collagen expression in renal interstitial in the untreated group were observed on the 7th day. Compared with the sham-operated group, percentages of area of TGF-β1,α- SMA, FN and LN expressions in the untreated group were markedly increased (P〈0. 05), while the percentage of area of interstitial fibrosis was decreased in the DLDD-treated group as compared with the untreated group (P〈0.05). On the 14th day, the percentages of area of TGF-β1, α-SMA, FN and LN expressions were declined in two treated groups as compared with the untreated group (P〈0. 05), but had no statistical difference in biochemical indicators, including BUN, SCr and 24-hour urinary protein. On the 21st day, the level of SCr and the percentage of area of TGF-β1 expression in the DLDD-treated group were lower than those of the enalapril-treated group (P〈0. 05).
Conclusion: DLDD can reduce the excretion of urinary protein and the degree of interstitial fibrosis, and significantly inhibit the expressions of TGF-β1,α-SMA, FN and LN. DLDD is superior to enalapril in protecting renal function after long-time application in rats.
出处
《中西医结合学报》
CAS
2008年第5期493-497,共5页
Journal of Chinese Integrative Medicine
基金
上海市医学发展基金资助项目(No2003ZD002)