Wang Lei, Wang Gang, Li Ting-qian
Department of Integrated Traditional Chinese and Western Medicine, Huaxi Hospital of Sichuan University, Chengdu.
Zhongguo Zhong Xi Yi Jie He Za Zhi. 2007 Jan;27(1):55-9.
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.
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.
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.
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.
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。
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。
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。
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。