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损伤后短期给予地塞米松治疗可抑制博来霉素诱导的大鼠肺纤维化。

Short course dexamethasone treatment following injury inhibits bleomycin induced fibrosis in rats.

作者信息

Dik W A, McAnulty R J, Versnel M A, Naber B A E, Zimmermann L J I, Laurent G J, Mutsaers S E

机构信息

Department of Immunology, Division of Neonatology, Erasmus MC, University Medical Centre Rotterdam, PO Box 1738, 3000 DR Rotterdam, The Netherlands.

出版信息

Thorax. 2003 Sep;58(9):765-71. doi: 10.1136/thorax.58.9.765.

Abstract

BACKGROUND

Corticosteroids are routinely used in patients with pulmonary fibrosis. The timing for initiation of treatment is likely to be crucial for corticosteroids to exert an antifibrotic effect. Experimental studies in animals have examined the effect of corticosteroid treatment starting before or at the time of lung injury. However, this is not representative of the human condition as treatment only begins after disease has been established. We examined the effect of a short course corticosteroid treatment starting 3 days after bleomycin induced lung injury on the development of pulmonary fibrosis.

METHODS

Bleomycin (1.5 mg/kg) was instilled intratracheally into rats to induce pulmonary fibrosis. The effect of a 3-day course of dexamethasone (0.5 mg/kg) initiated 3 days after bleomycin induced lung injury on cell proliferation and collagen deposition was examined by analysing bronchoalveolar lavage (BAL) fluid and lung tissue.

RESULTS

Treating bleomycin exposed animals after injury with dexamethasone for 3 days inhibited lung collagen deposition compared with animals exposed to bleomycin without dexamethasone treatment (15.2 (2.2) mg collagen/lung v 22.5 (2.1) mg/lung; p<0.05). Dexamethasone treatment reduced pulmonary parenchymal cell proliferation in bleomycin exposed rats but did not influence BAL fluid mitogenic activity for lung fibroblasts or alter the BAL fluid levels of the fibrogenic mediators transforming growth factor-beta(1), platelet derived growth factor-AB, and thrombin.

CONCLUSIONS

A 3 day course of dexamethasone treatment initiated 3 days after bleomycin induced lung injury reduces lung cell proliferation and collagen deposition by mechanisms other than through reduction of transforming growth factor-beta(1), platelet derived growth factor-AB, and thrombin levels in BAL fluid. We propose that an early short course treatment with dexamethasone may be useful in inhibiting pulmonary fibrosis.

摘要

背景

皮质类固醇常用于肺纤维化患者。对于皮质类固醇发挥抗纤维化作用而言,开始治疗的时机可能至关重要。动物实验研究了在肺损伤之前或之时开始皮质类固醇治疗的效果。然而,这并不代表人类的情况,因为治疗仅在疾病确立后才开始。我们研究了博来霉素诱导肺损伤3天后开始的短期皮质类固醇治疗对肺纤维化发展的影响。

方法

将博来霉素(1.5毫克/千克)经气管内注入大鼠以诱导肺纤维化。通过分析支气管肺泡灌洗(BAL)液和肺组织,研究在博来霉素诱导肺损伤3天后开始的为期3天的地塞米松(0.5毫克/千克)疗程对细胞增殖和胶原沉积的影响。

结果

与未用地塞米松治疗而暴露于博来霉素的动物相比,用地塞米松治疗博来霉素暴露后的动物3天可抑制肺胶原沉积(15.2(2.2)毫克胶原/肺对22.5(2.1)毫克/肺;p<0.05)。地塞米松治疗降低了博来霉素暴露大鼠的肺实质细胞增殖,但不影响BAL液对肺成纤维细胞的促有丝分裂活性,也未改变BAL液中促纤维化介质转化生长因子-β(1)、血小板衍生生长因子-AB和凝血酶的水平。

结论

在博来霉素诱导肺损伤3天后开始的为期3天的地塞米松治疗疗程,通过降低BAL液中转化生长因子-β(1)、血小板衍生生长因子-AB和凝血酶水平以外的机制,减少了肺细胞增殖和胶原沉积。我们提出,早期短期地塞米松治疗可能有助于抑制肺纤维化。

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