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过氧化氢在体外可使人类气道收缩:上皮细胞的作用。

Hydrogen peroxide contracts human airways in vitro: role of epithelium.

作者信息

Rabe K F, Dent G, Magnussen H

机构信息

Krankenhaus Grosshansdorf, Zentrum für Pneumologie und Thoraxchirurgie, Landesversicherungsanstalt Freie und Hansestadt Hamburg, Germany.

出版信息

Am J Physiol. 1995 Sep;269(3 Pt 1):L332-8. doi: 10.1152/ajplung.1995.269.3.L332.

DOI:10.1152/ajplung.1995.269.3.L332
PMID:7573466
Abstract

The effects of hydrogen peroxide (H2O2) on human airway smooth muscle tone were determined in vitro. Treatment with H2O2 led to transient concentration-related contractions in the organ bath, amounting to 118 +/- 14 mg (mean +/- SE; n = 12) at 1 mM H2O2, and to greater and more prolonged contractions under superfusion conditions, amounting to 451 +/- 71 mg (n = 17) at 1 mM H2O2. Epithelial removal augmented the response to H2O2 in both systems. Addition of catalase (500 U/ml) abolished the effects of H2O2. Pretreatment of superfused tissues with indomethacin (3 microM) shifted the concentration-effect curve to H2O2 rightward and almost abolished the response to 1 mM H2O2 in epithelium-intact preparations (n = 16; P < 0.05); the response in epithelium-denuded tissues was also significantly inhibited (n = 16; P < 0.05). Pretreatment of the tissues with the TP prostanoid-receptor antagonist GR-32191B (1 microM) also inhibited the contractile effect of H2O2 in epithelium-intact and -denuded tissues. In separate experiments, H2O2 resulted in concentration-related generation of prostaglandin (PG) D2 from isolated airway preparations. The amount of PGD2 released was not different in tissues with intact epithelium compared with those without (n = 9; NS). We conclude that H2O2 exerts on isolated human airways a contractile effect that is augmented by epithelium removal and is largely mediated by prostanoids. The source of PGD2 does not appear to be the epithelium, which we suggest serves mainly as a barrier against H2O2-mediated bronchoconstriction.

摘要

在体外测定了过氧化氢(H₂O₂)对人气道平滑肌张力的影响。用H₂O₂处理导致器官浴中出现短暂的浓度相关收缩,在1 mM H₂O₂时收缩量为118±14 mg(平均值±标准误;n = 12),在灌流条件下收缩更大且更持久,在1 mM H₂O₂时收缩量为451±71 mg(n = 17)。去除上皮细胞增强了两个系统中对H₂O₂的反应。添加过氧化氢酶(500 U/ml)可消除H₂O₂的作用。用吲哚美辛(3 μM)预处理灌流组织可使H₂O₂的浓度 - 效应曲线右移,并几乎消除了上皮完整制剂(n = 16;P < 0.05)对1 mM H₂O₂的反应;上皮剥脱组织中的反应也受到显著抑制(n = 16;P < 0.05)。用TP前列腺素受体拮抗剂GR - 32191B(1 μM)预处理组织也抑制了上皮完整和剥脱组织中H₂O₂的收缩作用。在单独的实验中,H₂O₂导致分离的气道制剂中前列腺素(PG)D₂的浓度相关生成。与无上皮组织相比,有完整上皮组织中释放的PGD₂量没有差异(n = 9;无显著性差异)。我们得出结论,H₂O₂对分离的人气道施加收缩作用,去除上皮细胞可增强该作用,且该作用主要由前列腺素介导。PGD₂的来源似乎不是上皮细胞,我们认为上皮细胞主要作为对抗H₂O₂介导的支气管收缩的屏障。

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