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大黄素干预大鼠胰腺纤维化过程中TGF-β1的动态研究 被引量:4

The TGF-β1 levels in rats with pancreatic fibrosis treated with emodin
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摘要 目的研究TGF-β1在大黄素抗大鼠胰腺纤维化过程中的作用。方法50只大鼠按完全随机法分成5组,每组10只。胰管内注射三硝基苯磺酸(TNBS)制备大鼠慢性胰腺炎模型,用不同剂量(20、40、80mg/kg)的大黄素鼻饲干预,0.9%NaCl注射液作为对照。Western印迹分析及免疫组化分析检测大鼠胰腺组织中的TGF-β1蛋白含量。结果与对照组比较,大黄素处理组TGF-β1蛋白表达量减少,尤其是大剂量大黄素处理组。结论TGF-β1在大黄素抗胰腺纤维化中起重要作用。 Objective To investigate the TGF-β1 levels in rats with pancreatic fibrosis treated with emodin. Methods Pancreatic fibrosis was induced by infusion of trinitrobenzene sulfonic acid (TNBS) into the pancreatic duct of rats. In emodin group he rats were fed with different doses of emodin (20, 40 and 80mg/kg body weight) , while in control group the rats received 0.9% sodium chloride solution. The tissue contents of TGF-β1 were measured by Western blotting and immunochemistry. Results Compare with control group, the emodin groups showed lower expression of TGF-β1, especially in high dose emodin group. Conclusion The anti-fibrosis effect of modin may be related to the TGF-β1.
出处 《浙江医学》 CAS 2007年第9期922-923,927,共3页 Zhejiang Medical Journal
关键词 大黄素 慢性胰腺炎 纤维化 TGF-Β1 Emodin Chronic Pancreatitis Fibrosis Tranforming Growth Factor-β1(TGF-β1)
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  • 1王皓,杨再兴,高春芳,万漠彬,王晓今,Senait Mengsteab,Axel M.Gressner,Ralf Weiskirchen.TGF-β1基因多态性与肝炎后肝纤维化的相关性研究[J].第二军医大学学报,2004,25(12):1284-1287. 被引量:5
  • 2Philips N, Keller T, Gonzalez S. TGF beta-like regulation of matrix metalloproteinases by anti-transforming growth factor-beta, and anti-transforming growth factor-beta 1 antibodies in dermal fibroblasts: implications for wound healing. Wound Repair Regen, 2004,12:53-59. 被引量:1
  • 3Arthur MJ. Fibrogenesis-II. metalloproteinases and their inhibitors in liver fibrosis. Am J Physiol Gastrointest Liver Physiol, 2000,279:245-249. 被引量:1
  • 4Hu MG, Hu GF, Kim Y, et al. Role of p12(CDK2-AP1) in transforming growth factor-beta1-mediated growth suppression. Cancer Res, 2004, 15:490-499. 被引量:1
  • 5de Caestecker M. The transforming growth factor-beta superfamily of receptors. Cytokine Growth Factor Rev, 2004,15:1-11. 被引量:1
  • 6Massague J, Wotton D. Transcriptional control by the TGF β/Smad signaling system. EMBO J, 2000, 19:1745-1754. 被引量:1
  • 7Dooley S, Hamzavi J, Breitkopf K, et al. Smad 7 prevents activation of hepatic stellate cells and liver fibrosis in rats. Gastroenterology, 2003,125:178-191. 被引量:1
  • 8Cutroneo KR, Phan SH. TGF-beta1-induced Smad 3 binding to the Smad 7 gene: knockout of Smad 7 gene transcription by sense phosphorothioate oligos, autoregulation, and effect on TGF-beta1 secretion: bleomycin acts through TGF-beta1. J Cell Biochem, 2003,89:474-483. 被引量:1
  • 9Flisiak R, Pytel-Krolezuk B, Prokopowicz D, et al. Circulating transforming growth factor beta1 as an indicator of hepatic function impairment in liver cirrhosis. Cytokine, 2000,12:677-681. 被引量:1
  • 10George J, Roulot D, Koteliansky VE, et al. In vivo inhibition of rat stellate cell activation by soluble transforming growth factor βtype Ⅱ receptor: a potential new therapy for hepatic fibrosis. Proc Natl Acad Sci U S A, 1999,96;12719-12724. 被引量:1

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