期刊文献+

参芪扶正注射液对内毒素致急性肺损伤大鼠肺组织Fractalkine表达的影响 被引量:10

Effect of Shenqi Fuzheng Injection on Fractalkine Expression in Lung Tissue of Rats with Lipopolysaccharide-induced Acute Lung Injury
暂未订购
导出
摘要 目的动态观察趋化因子Fractalkine(FKN)在内毒素(LPS)所致急性肺损伤(ALI)大鼠肺组织内表达水平的变化,和参芪扶正注射液对其的影响。方法经尾静脉注射LPS(4 mg/kg)建立ALI大鼠模型。将42只大鼠随机分为7组,每组6只:正常对照组、模型1、2、4 h 3个时相组和参芪扶正注射液1、2、4 h 3个时相组。采用酶联免疫吸附测定法(ELISA)、逆转录多聚酶链反应(RT-PCR)等方法,观察ALI大鼠模型肺组织病理学改变、肺湿干重比率(W/D)及血清肿瘤坏死细胞因子α(TNF-α)变化,检测肺组织FKN mR- NA的表达,同时观察参芪扶正注射液对上述指标的影响。结果(1)模型1、2、4 h组肺组织病理改变明显,肺损伤程度重,以2 h组最为显著,参芪扶正注射液能减轻ALI大鼠肺组织病理变化。(2)模型3个时相组肺W/D均明显增加,参芪扶正注射液能降低各时相组肺W/D值。(3)模型3个时相组血清TNF-α均明显增高,于2 h点达到最高值,参芪扶正注射液能显著降低各时点血清TNF-α水平(P<0.05)。(4)正常大鼠肺组织有FKN mRNA的表达,模型3个时相组肺组织FKN mRNA表达较正常组明显增加,在2 h时点达最高值,参芪扶正注射液能降低ALI大鼠肺组织FKN mRNA的表达(P<0.05)。FKN mRNA的表达与血清TNF-α水平呈正相关。结论早期使用参芪扶正注射液能改善ALI肺组织病理改变,减轻肺水肿,降低血清TNF-α水平,下调肺组织FKN mRNA的表达,对内毒素致急性肺损伤实验大鼠具有保护作用。 Objective To observe dynamically the Fraetalkine (FKN) expression in lung tissue of rats with lipopolysaccharide (LPS)-induced acute lung injury (ALI) and the effect of Shenqi Fuzheng Injection (SFI) on it. Methods Rat model of ALI was established by intravenous injection of 4 mg/kg of LPS. Forty-two Wistar rats were randomly divided into 7 groups, the normal group, the model group and the SFI group, the latter two were separated respectively into three time phases (the 1 h, 2 h and 4 h after modeling ) groups, 6 rats in each group, Pathological changes and wet/dry weight ratio (W/D) of lung were observed, serum TNF-α and FKN mRNA expression in the lung tissue were examined by ELISA and RT-PCR respectively. Results Severe pathological changes of lung presented in the model groups of all three time phases with a higher W/D ratio, as well as increased serum TNF-α level and FKN mRNA expression in lung tissue. The peak of abnormality of serum TNF-α level and FKN mRNA expression was shown in the 2 h time phase group. All the above-mentioned abnormal changes were alleviated after treatment in the SFI group (P〈0.05). In addition, the level of FKN mRNA expression was found to be positively correlated to the serum TNF-α concentration. Conclusion SFI treatment in early stage could relieve the pathological changes and edema in lung tissue, decrease serum TNF-α and down-regulate FKN mRNA expression, playing a protective role in LPS-induced ALI rats.
出处 《中国中西医结合杂志》 CAS CSCD 北大核心 2007年第1期55-59,共5页 Chinese Journal of Integrated Traditional and Western Medicine
基金 国家中医药管理局青年基金(No.04-05JQ03)
关键词 急性肺损伤 肿瘤坏死因子-α FRACTALKINE 参芪扶正注射液 acute lung injury tumor necrosis factor-a Fractalkine Shenqi Fuzheng Injection
  • 相关文献

参考文献17

  • 1Vincent JL,Sakr Y,Ranieri VM.Epidemiology and outcome of acute respiratory failure in intensive care unit patients.Crit Care Med 2003 ;31 (4 Suppl):S296-S299.
  • 2Rossi DL,Hardiman G,Copeland NG,et al.Cloning and characterization of a new type of mouse chemokine.Genomics 1998 ;47(2):163-170.
  • 3Fong AM,Erickson HP,Zachariah JP,et al.Ultrastructure and function of the fractalkine mucin domain in CX (3) C chemokine domain presentation.J Biol Chem 2000; 275 (6):3781-3786.
  • 4Yonedo O,Imai T,Goda S,et al.Fractalkine-mediated endothelial cell injury by NK cells.J Immunol 2000; 164 (8):4055-4062.
  • 5Goda S,Imai T,Yoshie O,et al.CX3C-chemokine,fractalkine-enhanced adhesion of THP-1 cells to endothelial cells through integrin-dependent and -independent mechanisms.J Immunol 2000; 164(8):4313-4320.
  • 6Wei YL,Jin EY,Lin X,et al.Effect of Korea red ginseng on acute lung injury of mice induced by LPS.Ginseng Rev 1999; 27:79.
  • 7李臣鸿,刘晓晴,张珍祥,李风雷,黄翠萍.急性肺损伤时黄芪对核因子κB及白细胞介素6mRNA表达的影响[J].中华结核和呼吸杂志,2002,25(3):189-189. 被引量:16
  • 8余维巍,刘晓晴.黄芪对内毒素性急性肺损伤大鼠肝细胞生长因子表达的影响[J].中国中西医结合急救杂志,2005,12(5):309-311. 被引量:7
  • 9中华医学会呼吸病学分会.急性肺损伤/急性呼吸窘迫综合征的诊断标准(草案)[J].中华结核和呼吸杂志,2000,23(4):203-203.
  • 10李新甫,汪建新.急性肺损伤动物模型研究进展[J].国外医学(呼吸系统分册),2005,25(7):506-508. 被引量:28

二级参考文献36

共引文献622

同被引文献141

引证文献10

二级引证文献126

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