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血小板活化因子可使雪貂气管平滑肌舒张,并降低体外跨上皮电位差。

Platelet-activating factor relaxes ferret tracheal smooth muscle and reduces transepithelial potential difference in vitro.

作者信息

Webber S E, Morikawa T, Widdicombe J G

机构信息

Department of Physiology, St George's Hospital Medical School, London.

出版信息

Br J Pharmacol. 1992 Jan;105(1):223-9. doi: 10.1111/j.1476-5381.1992.tb14238.x.

Abstract
  1. The effects of platelet activating factor (PAF) were examined on the smooth muscle tone, mucus volume, lysozyme and albumin outputs and potential difference (PD) across the ferret tracheal wall. 2. PAF (0.1-10 microM) had no direct effect on mucus volume, lysozyme or albumin output from the ferret trachea. PAF produced concentration-dependent relaxations of the tracheal smooth muscle and reductions in PD across the tracheal wall. There was no change in the histological appearance of the trachea after exposure to PAF. 3. The PAF-induced smooth muscle relaxation was not affected by FPL55712, a combination of mepyramine and cimetidine, or by a combination of the oxygen free-radical scavengers catalase and superoxide dismutase (SOD); but was abolished by indomethacin or the PAF-receptor antagonist WEB2086. 4. The PAF-induced reduction in PD was not affected by indomethacin, FPL55712 or mepyramine and cimetidine, but was prevented by catalase and SOD, and by WEB2086. 5. We conclude that PAF relaxes ferret tracheal smooth muscle in vitro by receptor-mediated release of a bronchodilator prostaglandin, possibly PGE2. PAF also reduces PD across the trachea suggesting changes in epithelial function; however, there is no histological epithelial damage after PAF. The reduction in PD with PAF is probably produced by receptor-mediated release of oxygen free-radicals. The cellular source of these free-radicals and of the dilator prostaglandin is unclear.
摘要
  1. 研究了血小板活化因子(PAF)对雪貂气管壁平滑肌张力、黏液量、溶菌酶和白蛋白分泌以及跨气管壁电位差(PD)的影响。2. PAF(0.1 - 10微摩尔)对雪貂气管的黏液量、溶菌酶或白蛋白分泌无直接影响。PAF可使气管平滑肌产生浓度依赖性舒张,并降低跨气管壁的PD。暴露于PAF后,气管的组织学外观无变化。3. PAF诱导的平滑肌舒张不受FPL55712(美吡拉敏和西咪替丁的组合)或氧自由基清除剂过氧化氢酶和超氧化物歧化酶(SOD)组合的影响;但吲哚美辛或PAF受体拮抗剂WEB2086可消除该作用。4. PAF诱导的PD降低不受吲哚美辛、FPL55712或美吡拉敏和西咪替丁的影响,但过氧化氢酶、SOD以及WEB2086可阻止该作用。5. 我们得出结论,PAF在体外通过受体介导释放支气管扩张性前列腺素(可能是PGE2)使雪貂气管平滑肌舒张。PAF还可降低跨气管的PD,提示上皮功能发生改变;然而,PAF作用后无组织学上皮损伤。PAF导致的PD降低可能是由受体介导释放氧自由基所致。这些自由基和扩张性前列腺素的细胞来源尚不清楚。

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