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在博来霉素诱导的大鼠肺泡炎中,支气管肺泡灌洗液中透明质酸的蓄积与铁、补体及粒细胞的耗竭无关。

Accumulation of hyaluronan in bronchoalveolar lavage fluid is independent of iron-, complement- and granulocyte-depletion in bleomycin-induced alveolitis in the rat.

作者信息

Nettelbladt O, Lundberg K, Tengblad A, Hällgren R

机构信息

Dept of Pulmonary Medicine, University Hospital, Uppsala, Sweden.

出版信息

Eur Respir J. 1990 Jul;3(7):765-71.

PMID:1702064
Abstract

Previous studies on bleomycin-induced alveolitis in rats have demonstrated a transient histological accumulation of hyaluronan (hyaluronate or hyaluronic acid) in the alveolar interstitium, corresponding to increases in hyaluronan (HA) levels in bronchoalveolar lavage (BAL) fluid and lung tissue extracts. The accumulation of HA was related to the influx of inflammatory cells, especially polymorphonucleated cells (PMNs) in BAL fluid and the increase in lung water. In this study we have investigated the influence of iron, complement and PMN dependent mechanisms on the early connective response of the lung in the bleomycin rat model. Iron depletion had no effect on HA or the cellular composition of lavage fluid recovered on day 4 post bleomycin. Treatment of bleomycin-injured rats with cobra venom factor (CVF), totally neutralized complement haemolytic activity but had no effect on lavage HA or the cell invasion in BAL. Treatment with anti-neutrophil serum (ANS), reduced blood and lavage PMN by 70-80%, but had no influence on HA levels in BAL. These results suggest that regulatory mechanisms other than those dependent on iron, complement activation or PMN recruitment are responsible for HA accumulation in this fibrosing alveolitis animal model.

摘要

以往关于博来霉素诱导大鼠肺泡炎的研究表明,肺泡间质中透明质酸(透明质酸盐或透明质酸)出现短暂的组织学积聚,这与支气管肺泡灌洗(BAL)液和肺组织提取物中透明质酸(HA)水平的升高相对应。HA的积聚与炎性细胞的流入有关,尤其是BAL液中的多形核细胞(PMN)以及肺含水量的增加。在本研究中,我们调查了铁、补体和PMN依赖性机制对博来霉素大鼠模型中肺早期结缔组织反应的影响。铁耗竭对博来霉素注射后第4天回收的灌洗液中的HA或细胞组成没有影响。用眼镜蛇毒因子(CVF)治疗博来霉素损伤的大鼠,完全中和了补体溶血活性,但对灌洗HA或BAL中的细胞浸润没有影响。用抗中性粒细胞血清(ANS)治疗,使血液和灌洗PMN减少70 - 80%,但对BAL中的HA水平没有影响。这些结果表明,在这种纤维化肺泡炎动物模型中,除了依赖铁、补体激活或PMN募集的调节机制外,还有其他调节机制负责HA的积聚。

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