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血小板活化因子对豚鼠气管气道液体形成及成分的影响。

Effect of platelet activating factor on formation and composition of airway fluid in the guinea-pig trachea.

作者信息

Rogers D F, Alton E W, Aursudkij B, Boschetto P, Dewar A, Barnes P J

机构信息

Department of Thoracic Medicine, National Heart & Lung Institute, London.

出版信息

J Physiol. 1990 Dec;431:643-58. doi: 10.1113/jphysiol.1990.sp018352.

Abstract
  1. We studied the effect of platelet activating factor (PAF) on leakage of albumin, and secretion of fucose (a marker for mucus glycoprotein) and protein into the tracheal lumen of the guinea-pig isolated in situ, and on bioelectric properties and fluxes of mannitol in vitro. We also studied the effect of PAF on mucus secretion in human bronchi in vitro. 2. In guinea-pig, intravenous PAF markedly increased the luminal concentration of protein but did not significantly increase fucose concentrations. Increased albumin leakage (274% above controls at a dose of 50 ng/kg PAF) was associated with the increased luminal content of protein (248% above controls at the same dose of PAF). 3. Leakage of albumin was maximal 10 min after PAF, was significantly reduced by 20 min and had returned to baseline by 30 min. This pattern of leakage could be repeated with successive administrations of PAF. 4. PAF induced small but significant biphasic changes in bioelectric properties in vitro. The initial response was rapid in onset and characterized by maximal increases in short-circuit current (Isc) of 6.5% above controls at 7.5 min and in conductance (G) of 7% at 20 min. Both responses were blocked by the PAF receptor antagonist WEB 2086. Amiloride blocked the increase in Isc. Permeability of the tissue to mannitol (Pmann) was unaltered. The delayed response was characterized by maximal increases in Isc and G of 10% above controls at 60-90 min which were not significantly affected by WEB 2086 or amiloride. Pmann was increased by 38% at 90 min. 5. PAF increased fucose secretion in human bronchi in vitro. 6. Lyso-PAF in vitro caused changes similar to those induced by PAF on bioelectric properties and mucus secretion, but had no significant effects in vivo. 7. Light microscopy showed no evidence of epithelial disruption in animals given intravenous PAF at a dose causing significant albumin transudation. 8. We conclude that PAF increases the protein content of guinea-pig tracheal fluid principally by inducing plasma leakage rather than mucus secretion and that the small changes in ion transport and epithelial conductance may reduce the tendency to epithelial disruption during plasma leakage.
摘要
  1. 我们研究了血小板活化因子(PAF)对白蛋白渗漏、岩藻糖(黏液糖蛋白的标志物)分泌以及蛋白质分泌到原位分离的豚鼠气管腔中的影响,还研究了其对体外生物电特性和甘露醇通量的影响。我们也研究了PAF对体外人支气管黏液分泌的影响。2. 在豚鼠中,静脉注射PAF显著增加了管腔内蛋白质浓度,但未显著增加岩藻糖浓度。白蛋白渗漏增加(在50 ng/kg PAF剂量下比对照组高274%)与相同剂量PAF下管腔内蛋白质含量增加(比对照组高248%)相关。3. PAF注射后10分钟白蛋白渗漏达到最大值,20分钟时显著降低,30分钟时恢复到基线水平。这种渗漏模式在连续注射PAF时可重复出现。4. PAF在体外诱导生物电特性出现小但显著的双相变化。初始反应起效迅速,特征为在7.5分钟时短路电流(Isc)比对照组最大增加6.5%,在20分钟时电导(G)增加7%。这两种反应均被PAF受体拮抗剂WEB 2086阻断。氨氯吡咪阻断了Isc的增加。组织对甘露醇的通透性(Pmann)未改变。延迟反应的特征是在60 - 90分钟时Isc和G比对照组最大增加10%,这不受WEB 2086或氨氯吡咪的显著影响。在90分钟时Pmann增加了38%。5. PAF增加了体外人支气管中岩藻糖的分泌。6. 体外溶血磷脂酸(Lyso - PAF)引起的变化与PAF诱导的生物电特性和黏液分泌变化相似,但在体内无显著影响。7. 光学显微镜检查显示,给予静脉注射PAF导致显著白蛋白渗出的剂量时,动物上皮无破坏迹象。8. 我们得出结论,PAF主要通过诱导血浆渗漏而非黏液分泌来增加豚鼠气管液中的蛋白质含量,并且离子转运和上皮电导的微小变化可能会降低血浆渗漏期间上皮破坏的倾向。 }

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