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首页> 外文期刊>Experimental and therapeutic medicine >Inhibition of fibrosis and inflammation by triple therapy with pirfenidone, edaravone and erythropoietin in rabbits with drug-induced lung injury: Comparison of CT imaging and pathological findings
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Inhibition of fibrosis and inflammation by triple therapy with pirfenidone, edaravone and erythropoietin in rabbits with drug-induced lung injury: Comparison of CT imaging and pathological findings

机译:吡非尼酮,依达拉奉和促红细胞生成素三联疗法对家兔药物性肺损伤的纤维化和炎症的抑制作用:CT成像与病理结果的比较

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In a rabbit model of bleomycin-induced lung injury, computed tomography (CT) and pathological studies were conducted to investigate whether the progression of this injury is inhibited by pirfenidone and by triple therapy with pirfenidone, edaravone and erythropoietin. We divided nine rabbits with bleomycin-induced lung injury into three equally sized groups. Group 1 served as the control, group 2 received pirfenidone alone and group 3 was treated with pirfenidone, edaravone and erythropoietin. Multidetector CT (MDCT) scans were acquired immediately after the administration of bleomycin, and further scans were performed on days 14 and 28. The area of abnormal opacity was calculated. The rabbit lungs were removed and the size of abnormal areas in macroscopic specimens was calculated and the degree of fibrosis and inflammation in microscopic specimens was scored. In order, the average size of the area of abnormal opacity on CT scans was largest in group 1, followed by groups 2 and 3. On day 28, the area of opacity was significantly smaller in group 3 than in group 1 (P=0.071). The average size of the area of abnormal opacity on macroscopic findings was largest in group 1, followed in order by groups 2 and 3; the difference between group 1 and 3 was significant (P<0.05). The average fibrosis score was highest in group 3 followed by groups 2 and 1. By contrast, the average inflammation score was highest in grou 2 followed by groups 1 and 3. Although the administration of pirfenidone alone slowed the progression of bleomycin-induced lung injury, the triple-drug combination was more effective.
机译:在博来霉素诱导的肺损伤的兔模型中,进行了计算机断层扫描(CT)和病理研究,以调查该损伤的进展是否被吡非尼酮和吡非尼酮,依达拉奉和促红细胞生成素的三联疗法抑制。我们将9例博来霉素诱导的肺损伤兔子分为三组。第1组为对照组,第2组仅接受吡非尼酮,第3组用吡非尼酮,依达拉奉和促红细胞生成素治疗。给予博来霉素后立即进行多探测器CT(MDCT)扫描,并在第14和28天进行进一步扫描。计算了不透明区域。去除兔子的肺并计算宏观标本中异常区域的大小,并对微观标本中的纤维化和炎症程度进行评分。因此,在CT扫描中,不透明区域的平均大小在第1组中最大,其次是第2和第3组。在第28天,第3组中的不透明区域显着小于第1组(P = 0.071) )。宏观发现的不透明区域的平均大小在第1组中最大,其次是第2组和第3组。第1组和第3组之间的差异是显着的(P <0.05)。平均纤维化评分在第3组中最高,其次是第2和第1组。相反,平均炎症评分在第2组中,其次是第1和第3组。尽管单独服用吡非尼酮可以减缓博来霉素诱发的肺损伤,三药组合更有效。

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