Salari H, Schellenberg R R
Department of Medicine, University of British Columbia, Vancouver, Canada.
Pulm Pharmacol. 1991;4(1):1-7. doi: 10.1016/0952-0600(91)90033-y.
Human airway epithelial cells grown to confluence were incubated with varying concentrations (10-100 microM) of arachidonic acid or platelet activating factor (PAF) for periods of 30 min to 24 h. Both stimuli caused the production of 15-hydroxyeicosatetraenoic acid (15-HETE) by epithelial cells as determined by HPLC. Neither stimulus caused the production of leukotrienes, thromboxane or prostaglandins aside from minimal amounts of PGE2. Maximal production of 15-HETE after arachidonic acid (10 microM; N = 9) occurred at 1 h (235 +/- 59 ng/mg protein), whereas maximum generation after PAF treatment (10 microM; N = 9) occurred at 6 h (153 +/- 48 ng/mg protein). Neither arachidonic acid nor PAF at concentrations up to 100 microM caused cell toxicity as determined by 51Cr release. 15-HETE at concentrations of greater than or equal to 0.1 microM contracted isolated human bronchus. An initial small amplitude, short-lasting (less than 15 min) contraction was followed by a much larger contraction beginning 30-60 min following 15-HETE challenge, reaching a maximum at approximately 2 hr. These results demonstrate that PAF may induce delayed airway smooth muscle contraction by the generation of 15-HETE from epithelial cells. The kinetics of 15-HETE generation and its contractile activity are compatible with it being a mediator of the late asthmatic reaction.
将生长至汇合状态的人气道上皮细胞与不同浓度(10 - 100微摩尔)的花生四烯酸或血小板活化因子(PAF)孵育30分钟至24小时。通过高效液相色谱法测定,两种刺激均导致上皮细胞产生15 - 羟基二十碳四烯酸(15 - HETE)。除了极少量的前列腺素E2外,两种刺激均未导致白三烯、血栓素或前列腺素的产生。花生四烯酸(10微摩尔;N = 9)刺激后15 - HETE的最大产量在1小时出现(235±59纳克/毫克蛋白质),而PAF处理(10微摩尔;N = 9)后最大产量在6小时出现(153±48纳克/毫克蛋白质)。通过51Cr释放测定,浓度高达100微摩尔的花生四烯酸和PAF均未引起细胞毒性。浓度大于或等于0.1微摩尔的15 - HETE使离体人支气管收缩。最初是小幅度、持续时间短(小于15分钟)的收缩,随后在15 - HETE刺激后30 - 60分钟开始出现幅度大得多的收缩,在约2小时达到最大值。这些结果表明,PAF可能通过上皮细胞产生15 - HETE诱导气道平滑肌延迟收缩。15 - HETE产生的动力学及其收缩活性与它作为迟发性哮喘反应的介质相符。