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[参芪扶正注射液对脂多糖诱导的大鼠急性肺损伤肺组织中趋化因子表达的影响]

[Effect of Shenqi Fuzheng injection on fractalkine expression in lung tissue of rats with lipopolysaccharide-induced acute lung injury].

作者信息

Wang Lei, Wang Gang, Li Ting-qian

机构信息

Department of Integrated Traditional Chinese and Western Medicine, Huaxi Hospital of Sichuan University, Chengdu.

出版信息

Zhongguo Zhong Xi Yi Jie He Za Zhi. 2007 Jan;27(1):55-9.

Abstract

OBJECTIVE

To observe dynamically the Fractalkine (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-alpha 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-alpha level and FKN mRNA expression in lung tissue. The peak of abnormality of serum TNF-alpha 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-alpha concentration.

CONCLUSION

SFI treatment in early stage could relieve the pathological changes and edema in lung tissue, decrease serum TNF-alpha and down-regulate FKN mRNA expression, playing a protective role in LPS-induced ALI rats.

摘要

目的

动态观察脂多糖(LPS)诱导的急性肺损伤(ALI)大鼠肺组织中趋化因子(FKN)的表达及参芪扶正注射液(SFI)对其的影响。

方法

通过静脉注射4mg/kg LPS建立ALI大鼠模型。42只Wistar大鼠随机分为7组,即正常组、模型组和SFI组,后两组再分别分为建模后1h、2h和4h三个时间点的亚组,每组6只。观察肺组织病理变化及肺湿/干重比(W/D),分别采用酶联免疫吸附测定(ELISA)和逆转录-聚合酶链反应(RT-PCR)检测血清肿瘤坏死因子-α(TNF-α)水平及肺组织FKN mRNA表达。

结果

三个时间点的模型组肺组织均出现严重病理改变,W/D比值升高,血清TNF-α水平及肺组织FKN mRNA表达增加。血清TNF-α水平及FKN mRNA表达异常峰值出现在2h时间点组。SFI组治疗后上述异常改变均减轻(P<0.05)。此外,发现FKN mRNA表达水平与血清TNF-α浓度呈正相关。

结论

早期给予SFI治疗可减轻肺组织病理改变和水肿,降低血清TNF-α水平,下调FKN mRNA表达,对LPS诱导的ALI大鼠起保护作用。

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