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新城疫病毒对CCl_4诱导的小鼠肝纤维化的抑制作用研究

Inhibitory effect of Newcastle disease virus on hepatic fibrosis induced by CCl_4
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摘要 目的观察新城疫病毒(NDV)对CCl4诱导的小鼠肝纤维化的抑制作用。方法昆明小鼠腹腔注射CCl4/花生油溶液,每周2次,连续8周,制作肝纤维化模型。最后一次CCl4注射后3d由尾静脉注射NDV 1次或3次,每次注射间隔24h,注射完毕24h后处死动物。取出肝脏进行大体形态观察,行HE和天狼猩红染色观察肝组织病理学改变,Western blotting检测肝组织中α-平滑肌肌动蛋白(α-SMA)的表达。结果 CCl4诱导8周后,小鼠肝脏出现明显纤维化表现,可见肝脏质硬、表面粗糙不平、大量密集分布的白色点状斑块。HE染色显示纤维化肝脏组织结构松散,窦周隙增大。天狼猩红染色显示胶原异常沉积。而NDV注射3次后,小鼠肝脏表面白色斑点显著减少,胶原沉积降低。Western blotting结果表明,α-SMA表达水平随NDV注射次数增加而降低。结论 NDV能有效抑制CCl4诱导的小鼠肝纤维化的发生发展。 Objective To explore the inhibitory effect of Newcastle diseases virus (NDV) on CCl4-induced liver fibrosis in mice. Methods Liver fibrosis model was reproduced in 30 Kunming mice by intraperitoneal injection of CCl4/peanut oil solution for 2 times a week, and the total treatment lasted for 8 weeks. Three days after last injection, NDV was injected through tail vein for 1 or 3 times (24h intervals). Twenty-four hours after NDV infusion, mice were sacrificed and the livers were removed for gross morphology observation. The liver tissue sections were stained by HE and Sirius red dyeing, α-smooth muscle actin (α-SMA) expression was detected by Western blotting. Results After CCl4 induction for 8 weeks, obvious fibrosis symptoms appeared in the liver of model mice, and the surface of liver tissue became hard with rough, with white patches on it. HE staining showed that there was loosening of tissue and enlarged perisinusoidal spaces in liver with fibrosis. Sirius red dyeing displayed abnormal collagen deposition in the fibrotic liver tissues. After NDV injection for 3 times, white spots on the surface of mouse liver were significantly reduced, and collagen deposition was lowered. Western blotting showed that α-SMA levels decreased with increasing frequency of NDV injection. Conclusion NDV may effectively suppress the development of CCl4-induced liver fibrosis in mice.
作者 李亚琳
出处 《解放军医学杂志》 CAS CSCD 北大核心 2013年第11期885-887,共3页 Medical Journal of Chinese People's Liberation Army
基金 陕西省教育厅资助项目(009JK427) 渭南师范学院基金资助项目(10YKZ054)~~
关键词 新城疫病毒 肝硬化 实验性 四氯化碳 newcastle disease virus liver cirrhosis, experimental carbon tetrachloride
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参考文献13

  • 1李亚琳.新城疫病毒在肿瘤治疗中的研究进展[J].动物医学进展,2012,33(8):97-100. 被引量:2
  • 2任臻,尉丁,南刚,胡福泉,陈志南,边惠洁.新城疫病毒Italien株辅助质粒的构建及功能鉴定[J].解放军医学杂志,2012,37(7):702-706. 被引量:1
  • 3McGregor DD, Logie PS, Carmichael LE. The mediator of cellular immunity. Ⅻ. Inhibition of activated T cells by Newcastle disease virus[J].J Exp Med, 1976, 144(3): 627-643.
  • 4F~bi~tn Z, Csatary CM, Szeber6nyi J, et al. pS3-independent endoplasmic reticulum stress-mediated cytotoxicity of a Newcastle disease virus strain in tumor cell lines[J]. J Virol, 2007, 81(6): 2817-2830.
  • 5李亚琳.新城疫病毒感染活化的人肝星状细胞系LX-2[J].基础医学与临床,2012,32(10):1161-1166. 被引量:1
  • 6Bai T, Lian LH, Wu YL, et al. Thymoquinone attenuates liver fibrosis via PI3K and TLR4 signaling pathways in activated hepatic stellate cells [J]. Int Immunopharmacol, 2013, 15 (2): 275-281.
  • 7Kaji K, Yoshiji H, Ikenaka Y, et al. Dipeptidyl peptidase-4 inhibitor attenuates hepatic fibrosis via suppression of activated hepatic stellate cell in rats[J]. J Gastroenterol, 2013, [Epub ahead of print].
  • 8Akpolat N, Yahsi S, Godekmerdan A, et al. The value of α -SMA in the evaluation of hepatic fibrosis severity in hepatitis B infection and cirrhosis development: a histopathotogical and immunohistochemical study[J]. Histopathology, 2005, 47(3): 276-280.
  • 9Dong R, Luo Y, Zheng S. α -SMA overexpression associated with increased liver fibrosis in infants with biliary atresia[J]. J Pediatr Gastroenterol Nutr, 2012, 55(6): 653-656.
  • 10郝礼森,张晓岚,周智宏,李玉林,麻继臣,安君艳,姚冬梅,房澍名,姜慧卿.胆汁淤积性肝纤维化大鼠肝组织中PTEN表达与肝星状细胞凋亡的关系研究[J].解放军医学杂志,2010,35(7):836-838. 被引量:9

二级参考文献58

  • 1孙迎春,金宁一,米志强,李霄,连海,李萍.新城疫病毒HN基因诱导肝癌细胞SMMC7721凋亡的作用机制[J].中华肿瘤杂志,2005,27(5):279-282. 被引量:5
  • 2张华,边惠洁,尉丁,李亚琳,杨滨,陈志南.天然溶瘤新城疫病毒Italien株HN基因真核表达载体的构建和表达[J].解放军医学杂志,2007,32(2):100-103. 被引量:1
  • 3Watanabe S, Horie Y, Kataoka E, etal. Non-alcoholic steatohepatitis and hepatocellular carcinoma: lessons from hepatocyte-specific phosphatase and tensin homolog (PTEN)-deficient mice[J]. J Gastroenterol Hepatol, 2007, 22(Suppl 1): S96-S100.
  • 4Moezi L, Gaskari SA, Liu H, et al. Anandamide mediates hyperdynamic circulation in cirrhotic rats via CB(1) and VR(1) receptors[J]. Br J Pharmacol, 2006, 149(7) : 898-908.
  • 5Zhang J, You H, Wang T, etal. Triple-staining to identify apoptosis of hepatic cells in situ[J]. J Nippon Med Sch, 2000, 67(4) : 280- 283.
  • 6Urtasun R, Nieto N. Hepatic stellate cells and oxidative stress[J]. Rev Esp Enferm Dig, 2007, 99(4): 223-230.
  • 7Elsharkawy AM, Oakley F, Mann DA. The role and regulation of hepatic stellate cell apoptosis in reversal of liver fibrosis[J]. Apoptosis, 2005, 10(5) : 927-939.
  • 8Issa R, Williams E, Trim N, et al. Apoptosis of hepatic stellate cells: involvement in resolution of biliary fibrosis and regulation by .soluble growth factors[J]. Gut, 2001, 48(4): 548-557.
  • 9Gressner AM. The up-and-down of hepatic stellate cells in tissue injury: apoptosis restores cellular homeostasis[J]. Gastroenterology, 2001, 120(5): 1285-1288.
  • 10Osada N, Mochida S, Inao M, et al. Apoptosis in dissociation between DNA synthesis and cellular functions of activated hepatic stellate cells-a study with carbon tetraehloride-indueed rat liver injury [J]. Bioehem Biophys Res Commun, 2001, 282(2): 524-528.

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