Zhang Yan-ping, Fan Mao-rong, Wang Shu-chen
Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing.
Zhongguo Zhong Xi Yi Jie He Za Zhi. 2007 Nov;27(11):1013-5.
To study the effect of Feixianping (FXP) on collagen type I and II in rats with pulmonary fibrosis (PF).
Sixty healthy male SD rats were randomly divided into 5 groups, the normal group (A), the model group (B), the positive control group (C) and the two FXP groups (D and E) treated respectively with high and low dose of FXP. Except those in Group A (they were not modeled and administered with normal saline), all rats were established into PF model by intra-tracheal instillation of bleomycin and administered with respective medicines starting from the 1st day after modeling. Rats were sacrificed in batches at 3 time points, the 7th, 14th, and 28th day for observing the pathological changes of lung under light microscope with HE staining and to identify collagen type I and III in lung tissue by immunohistochemical stain and image quantitative analysis.
Light-dyeing proliferative collagen fiber was presented in the slightly thickened alveolar wall in lung of modeled rats from the 14th day on, and the pathological changes became more distinct on the 28th day. The highest amount of collagen appeared in the group B, correspondingly, that in all the other groups was much lower (P < 0.05). Reduction of collagen type I and III revealed in both FXP treated groups, but better effect was shown in the high dose FXP group. The effect of FXP was superior to that of positive control on the 14 th day (P <0.05).
FXP can effectively reduce the abnormal proliferation of collagen in experimental rats with PF.
研究肺纤宁(FXP)对肺纤维化(PF)大鼠Ⅰ型和Ⅱ型胶原的影响。
将60只健康雄性SD大鼠随机分为5组,即正常组(A组)、模型组(B组)、阳性对照组(C组)以及分别给予高、低剂量FXP的两个FXP组(D组和E组)。除A组大鼠不造模且给予生理盐水外,其余大鼠均通过气管内滴注博来霉素建立PF模型,并于造模后第1天开始给予相应药物。在第7天、第14天和第28天这3个时间点分批处死大鼠,用HE染色观察肺组织病理变化,通过免疫组织化学染色和图像定量分析鉴定肺组织中的Ⅰ型和Ⅲ型胶原。
造模大鼠肺组织从第14天起肺泡壁轻度增厚,可见淡染的增殖性胶原纤维,第28天病理变化更明显。B组胶原含量最高,相应地,其他各组胶原含量均低得多(P<0.05)。两个FXP治疗组的Ⅰ型和Ⅲ型胶原均减少,但高剂量FXP组效果更好。在第14天,FXP的效果优于阳性对照组(P<0.05)。
FXP可有效减少实验性PF大鼠胶原的异常增殖。