Brunelleschi S, Haye-Legrand I, Labat C, Norel X, Benveniste J, Brink C
Institut National de la Santé Recherche Médicale, University of Paris-Sud, Clamart, France.
J Pharmacol Exp Ther. 1987 Oct;243(1):356-63.
A fixed concentration of paf-acether (platelet-activating factor; 4 microM) relaxed isolated guinea pig tracheal preparations which had been contracted with histamine (50 microM), serotonin (1 microM) or leukotriene D4 (0.1 microM). The relaxations were approximately 43, 100 and 57%, respectively. We did not observe any relaxant effect of paf-acether (4 microM) in tissues contracted with acetylcholine (50 microM). Both lyso paf-acether (10 microM) and bovine serum albumin (25 micrograms/ml) were without effect on histamine-contracted preparations. In the presence of indomethacin (1.7 microM; 30 min) or aspirin (0.1 mM; 30 min) the relaxant effect of paf-acether (4 microM) in tissues contracted with histamine was significantly reduced to approximately 10 and 12%, respectively. When paf-acether (4 microM) was added to histamine-contracted tracheal preparations in the presence of noradrenaline (0.1 microM) or prostaglandin E2 (PGE2, 10 nM) the relaxations were 62 and 82%, respectively. Noradrenaline and PGE2 alone had only a slight relaxant effect in these tissues (7 and 14%, respectively). In the presence of indomethacin (1.7 microM) the synergistic effect of paf-acether and PGE2 was still observed. The basal production of PGE2 in isolated guinea pig tracheal preparations was 4.6 +/- 1.4 pg/mg of tissue. In the presence of paf-acether (4 microM) increased levels of this prostanoid were detected (11.2 +/- 2.4 pg/mg of tissue). Isolated guinea pig tracheal preparations when contracted with histamine released PGE2 (17.6 +/- 4.1 pg/mg of tissue). In the presence of histamine and paf-acether there was a significant increase in detectable levels of PGE2 (48.6 +/- 13.2 pg/mg of tissue).(ABSTRACT TRUNCATED AT 250 WORDS)
固定浓度的血小板活化因子(PAF - 乙酰醚;4微摩尔)可使已被组胺(50微摩尔)、5 - 羟色胺(1微摩尔)或白三烯D4(0.1微摩尔)收缩的豚鼠离体气管标本舒张。舒张率分别约为43%、100%和57%。我们未观察到PAF - 乙酰醚(4微摩尔)对已被乙酰胆碱(50微摩尔)收缩的组织有任何舒张作用。溶血PAF - 乙酰醚(10微摩尔)和牛血清白蛋白(25微克/毫升)对组胺收缩的标本均无作用。在吲哚美辛(1.7微摩尔;30分钟)或阿司匹林(0.1毫摩尔;30分钟)存在的情况下,PAF - 乙酰醚(4微摩尔)对组胺收缩组织的舒张作用分别显著降低至约10%和12%。当在去甲肾上腺素(0.1微摩尔)或前列腺素E2(PGE2,10纳摩尔)存在的情况下,将PAF - 乙酰醚(4微摩尔)添加到组胺收缩的气管标本中时,舒张率分别为6,2%和82%。单独的去甲肾上腺素和PGE2在这些组织中仅有轻微的舒张作用(分别为7%和14%)。在吲哚美辛(1.7微摩尔)存在的情况下,仍可观察到PAF - 乙酰醚和PGE2的协同作用。豚鼠离体气管标本中PGE2的基础生成量为4.6±1.4皮克/毫克组织。在PAF - 乙酰醚(4微摩尔)存在的情况下,检测到该类前列腺素水平升高(11.2±2.4皮克/毫克组织)。豚鼠离体气管标本在被组胺收缩时会释放PGE2(17.6±4.1皮克/毫克组织)。在组胺和PAF - 乙酰醚存在的情况下,可检测到的PGE2水平显著升高(48.6±13.2皮克/毫克组织)。(摘要截短于250字)