Rasmussen J B, Eriksson L O, Tagari P, Margolskee D J, Girard Y, Andersson K E
Department of Pulmonary Medicine, University of Lund, Malmö General Hospital, Sweden.
Allergy. 1992 Dec;47(6):599-603. doi: 10.1111/j.1398-9995.1992.tb02381.x.
Leukotriene (LT) E4 represents the major LT metabolite in man, and its urinary excretion can be used as an indirect marker of systemic LTC4 and/or LTD4 synthesis and release. In the present study LTE4 excretion was monitored for 24 h in 12 atopic patients with mild asthma undergoing antigen bronchoprovocation as part of a double-blind, placebo-controlled, two-period cross-over study of the aerosol-delivered LTD4 antagonist, L-648,051. Urinary LTE4 excretion was also studied separately in six of the patients after inhaling only diluent. Urine was sampled before, and serially after antigen challenge, at intervals corresponding to the immediate (0-3 h postchallenge) and late (3-6, 6-12, 12-24 h postchallenge) asthmatic reactions. LTE4 was determined by reversed-phase HPLC and radioimmunoassay. Forced expiratory volume in 1 s (FEV1) was recorded serially through 8 h after inhalation of antigen and diluent. Compared to base-line measurements, antigen bronchoprovocation induced significant increases in mean LTE4 excretion rates 0-3 h postchallenge (i.e. during the immediate asthmatic response) after treatment with both placebo (P < 0.01) and L-648,051 (P < 0.05). These mean LTE4 excretion rates in the immediate phase were also significantly higher than the mean rates in the late phase (3-6 h and beyond); the excretion rates of LTE4 at these later time intervals were similar to base-line values. After inhalation of diluent, the LTE4 excretion rates in the intervals 0-3, 3-6, 6-12 and 12-24 h were unchanged from base-line values.(ABSTRACT TRUNCATED AT 250 WORDS)
白三烯(LT)E4是人体中主要的LT代谢产物,其尿排泄可作为全身LTC4和/或LTD4合成与释放的间接标志物。在本研究中,作为一项关于雾化递送的LTD4拮抗剂L-648,051的双盲、安慰剂对照、两阶段交叉研究的一部分,对12名患有轻度哮喘的特应性患者进行抗原支气管激发试验,并监测其24小时的LTE4排泄情况。还对其中6名患者仅吸入稀释剂后进行了单独的尿LTE4排泄研究。在抗原激发前及激发后按顺序采样尿液,采样间隔对应于速发(激发后0 - 3小时)和迟发(激发后3 - 6、6 - 12、12 - 24小时)哮喘反应。通过反相高效液相色谱法和放射免疫测定法测定LTE4。在吸入抗原和稀释剂后连续8小时记录1秒用力呼气量(FEV1)。与基线测量相比,在用安慰剂(P < 0.01)和L-648,051(P < 0.05)治疗后,抗原支气管激发在激发后0 - 3小时(即速发哮喘反应期间)引起平均LTE4排泄率显著增加。速发期的这些平均LTE4排泄率也显著高于迟发期(3 - 6小时及以后)的平均排泄率;在这些较晚时间间隔的LTE4排泄率与基线值相似。吸入稀释剂后,0 - 3、3 - 6、6 - 12和12 - 24小时的LTE4排泄率与基线值无变化。(摘要截选至250字)