期刊文献+

隔药灸和电针对克罗恩病大鼠结肠IGF-I、IGF-IR、IGFBP-5表达的影响 被引量:19

Effects of Herbs-partitioned Moxibustion and Electro-acupuncture on Expressions of IGF-I、IGF-IR and IGFBP-5 in Crohn’s Disease Rats
下载PDF
导出
摘要 目的研究隔药灸和电针对克罗恩病大鼠结肠IGF-I、IGF-IR、IGFBP-5蛋白及IGF-I mRNA的调节作用,探讨针灸治疗大鼠克罗恩病肠纤维化的作用机制。方法SD大鼠随机分为正常组、模型组、隔药灸组、电针组和药物组。采用三硝基苯磺酸制备大鼠克罗恩病模型,应用HE染色、Masson染色光镜下观察结肠病理组织学变化及胶原纤维增生情况;采用实时荧光定量聚合酶链反应检测结肠IGF-I mRNA的变化;采用免疫组织化学Envision法检测结肠IGF-I、IGF-IR、IGFBP-5蛋白表达变化。结果与正常组比较,模型组大鼠结肠组织胶原增生,IGF-I、IGF-IR、IGFBP-5蛋白表达均显著增加,IGF-I mRNA表达显著增加。经治疗后,与模型组比较隔药灸组、电针组、药物组大鼠结肠胶原增生均显著减少,隔药灸组较电针组作用显著。隔药灸组、电针组、药物组大鼠IGF-I、IGF-IR、IGFBP-5蛋白表达均显著降低;隔药灸组对IGF-I、IGFBP-5蛋白的下调作用优于电针组。隔药灸组、药物组IGF-I mRNA表达均显著降低,电针组变化不明显。结论隔药灸和电针能够下调结肠IGF-I、IGF-IR、IGFBP-5蛋白的异常表达,该作用可能是隔药灸和电针改善克罗恩病肠纤维化的重要机制。隔药灸能够下调IGF-I mRNA表达,对IGF-I、IGFBP-5蛋白的下调作用优于电针,该作用可能是其改善克罗恩病肠纤维化优于电针的机制之一。 Objective To explore the mechanism of acupuncture and moxibustion on treating fibrosis in colon of Crohn' s disease (CD) rats by investigating the regulating action of electro-acupuncture and herbs-partitioned moxibustion on the expressions of insulin- like growth factor-I (IGF-I) ,insulin-like growth factor-I receptor (IGF-IR) and insulin-like growth factor binding, protein-5 (IGFBP- 5 ). Methods Sprague-Dawley rats were randomly divided into normal group, model group, herbs- partitioned moxibustion group, electro-acupuncture group and medication group. CD rat models were made by 2,4,6-trlnitrobenzene sulfonic acid. Pathologic histology changes of colon were observed under light microscope with HE stain and Masson stain. The expression of IGF-I mRNA was detected by real-time fluorescence quantitative polymerase chain reaction(FQ-PCR). The expressions of IGF-I,IGF-IR and IGFBP-5 protein were determined by Envision immunohistochemical method. Results Compared with normal group, the collagen hyperplasy and expressions of IGF-I, IGF-IR, IGFBP-5 protein and IGF-I mRNA in colon were significantly increased in the model group. After treatment, collagen hyperplasy decreased significantly in herbs- partitioned moxibustion group, electro-acupuncture group and medication group compared with model group. The effect in herbs-partitioned moxibustion group is better than that in electro-acupuncture group. The expressions of IGF-I ,IGF-IR ,IGFBP-5 protein decreased significantly in herbs-partitioned moxibustion group, electro-acupuncture group and medication group, the expressions of IGF-I ,IGFBP-5 protein decreased more in herbs-partitioned moxibustion group than in electro-acupuncture group. The expression of IGF-I mRNA decreased significantly in herbs-partition moxibustion group and medication group while which in electro-acupuncture group had no statistical change. Conclusion Herbs-partitioned moxibustion and electro-acupuncture could decrease the abnormal protein expressions of IGF-I ,IGF-IR ,IGFBP-5, which may be the important mechanism of herbs-partition group and electro-acupuncture group in decreasing fibrosis of CD rats' colons. Herbs-partition moxibustion could decrease the expres- sions of IGF-I mRNA, and it is prior to the electro-acupuncture group in decreasing the expressions of IGF-I,IGFBP-5 protein which possibly lead to a better effect in improvement of fibrosis in herbs-partition moxibustion group.
出处 《上海针灸杂志》 2008年第5期37-40,共4页 Shanghai Journal of Acupuncture and Moxibustion
基金 国家自然科学基金资助项目(NO30400609) 上海市重点学科建设资助项目(T0302)
关键词 克罗恩病 肠纤维化 IGF—I IGF—IR IGFBP-5 间接灸 电针 Crohn disease Intestinal fibrosis IGF-I IGF-IR IGFBP-5 Indirect moxibustion Electro-acupuncture
  • 相关文献

参考文献13

  • 1Fiocchi C.Inflammatory bowel disease:Etiology and pathogenesis[J].Gastroenterology,1998,115:182-205.
  • 2巫协宁,刘爱群.克罗恩病肠壁纤维化的检测、意义和成因[J].中华消化杂志,2007,27(3):210-211. 被引量:8
  • 3Lawrance IC,Maxwell L,Doe W.Altered response of intestinal mucosal fibroblasts to profibrogenic cytokines in inflammatory bowel disease[J].Inflamm Bowel Dis,2001,7(3):226-236.
  • 4谭琳蓥,吴焕淦,刘慧荣,江彬,黄文燕,张必萌,施征.IGF与肠纤维化的关系及针灸的调节作用研究进展[J].上海中医药大学学报,2006,20(1):76-78. 被引量:6
  • 5Morris JP,Beck PL,Herridege MS,et al.Hapten-induced model of chronic inflammation and ulceration in the rat colon[J].Gastroenterology,1989,96:795-803.
  • 6徐淑云.药理学实验方法学[M].北京:人民卫生出版社,1991:713-723.
  • 7施茵,吴焕淦.隔药饼灸治疗克隆氏病的临床研究[J].江西中医药,2003,34(8):16-17. 被引量:14
  • 8Lund PK,Zimmermann EM.Insulin-like growth factors and inflammatory bowel disease[J].Baillieres Clin Gastroenterol,1996,(10):83-96.
  • 9Sanz S,Pucilowska JB,Liu S,et al.Expression of insulin-like growth factor Ⅰ by activated hepatic stellate cells reduces fibrogenesis and enhances regeneration after liver injury[J].Gut,2005,54(1):134-141.
  • 10Chetty A,Cao GJ,Nielsen HC.Insulin-like Growth Factor-Ⅰ signaling mechanisms.type Ⅰ collagen and alpha smooth muscle actin in human fetal lung fibroblasts[J].Pediatr Res,2006,60(4):389-394.

二级参考文献46

  • 1WU Huan-gan AN Guang-qing LIU Hui-rong SHI Zheng CHEN Han-ping LIU Shi-min SHI Yin XIAO Yuan-chun.Clinical Study on the Prevention and Treatment of Intestinal Fibrosis in Ulcerative Colitis by Moxibustion[J].Journal of Acupuncture and Tuina Science,2003,1(2):14-17. 被引量:14
  • 2巫协宁,周怡和,朱国清,周育德.克罗恩病的治疗策略[J].中华消化杂志,2005,25(5):296-298. 被引量:13
  • 3全国慢性非感染性肠道疾病学术研讨会.克隆病的诊断与鉴别[J].中华消化杂志,1993,13:372-372.
  • 4Clemmons DR.Role of insulin-like growth factor binding proteins in controlling IGF actions[J].Mol Cell Endocrinol,1998,140(1-2):19-24.
  • 5De Alava E,Panizo A,Antonescu CR,et al.Association of EWS-FLI1 type 1 fusion with lower proliferative rate in Ewing's sarcoma[J].Am J pathol,2000,156(3):849-885.
  • 6Rechler MM.Insulin-like growth factor binding proteins[J].Vitam Horm,1993,47(3):1-114.
  • 7Haluzik M,Yakar S,Gavrilov O,et al.Insulin resistance in the liver-specific IGF-1 gene-deleted mouse is abrogated by deletion of the acid-labile subunit of the IGF-binding protein-3 complex:relative roles of growth hormone and IGF-1 in insulin resistance[J].Diabetes,2003,52 (10):2483-2489.
  • 8Lund PK.IGFs and the digestive tract:the insulin-like growth factors system[A].In:The IGF System[M].Totowa,NJ:Humana Press,1999,517-544.
  • 9Fruchtman S,Simmons JG,Wilkins HR,et al.SOCS-2 deficiency leads to increased intestinal collagen deposition and STAT3 activation in a mouse model of mucosal injury,inflammation and repair[J].Gastroenterology,2002,122(5):862-867.
  • 10Miller ME,Michaylira CZ,Simmons JG,et al.Suppressor of cytoline signaling-2:a growth hormone inducible inhibitor of intestinal epithelial cell proliferation[J].Gastroenterology,2004,127 (2):570-581.

共引文献26

同被引文献293

引证文献19

二级引证文献360

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部