Bolton P B, Lefevre P, McDonald D M
Department of Anatomy, University of California, San Francisco 94143-0130, USA.
Am J Respir Crit Care Med. 1997 Apr;155(4):1428-35. doi: 10.1164/ajrccm.155.4.9105089.
We examined the effect of salmeterol, a long-acting beta2-adrenergic receptor agonist, on ovalbumin-induced plasma leakage and leukocyte adhesion in tracheal blood vessels of unanesthetized brown Norway rats. Ovalbumin challenge of sensitized rats resulted in both early and late phases of plasma leakage as measured with Evans blue. The early phase occurred during the challenge. The late phase began 2 h after the challenge, peaked at 4 h, and ended by 24 h. Ovalbumin challenge also increased the number of adherent leukocytes in mucosal blood vessels at 4 h. Nebulized salmeterol (5 mg/ml for 10 min) administered before the challenge inhibited the early-phase leak by 26%, 58%, or 85%, depending upon whether the interval between pretreatment and challenge was 0.5, 1, or 4.5 h, respectively. Similarly, salmeterol pretreatment (0.05 to 5 mg/ml for 10 min) reduced the late-phase leak at 4 h. Late-phase leakage was completely blocked at concentrations of 0.5 mg/ml or greater. This inhibitory effect was prevented by prior injection of the beta2-adrenergic receptor antagonist ICI-118,551. Salmeterol pretreatment also reduced the adherence of neutrophils, eosinophils, monocytes, and lymphocytes in mucosal blood vessels at 4 h. We conclude that salmeterol pretreatment can reduce the plasma leakage and leukocyte adhesion in early- and late-phase responses after antigen challenge through its action on beta2 receptors.
我们研究了长效β2肾上腺素能受体激动剂沙美特罗对未麻醉的棕色挪威大鼠气管血管中卵清蛋白诱导的血浆渗漏和白细胞黏附的影响。用伊文思蓝测定,致敏大鼠接受卵清蛋白激发后出现了血浆渗漏的早期和晚期阶段。早期阶段发生在激发过程中。晚期阶段在激发后2小时开始,4小时达到峰值,并在24小时结束。卵清蛋白激发还使4小时时黏膜血管中黏附的白细胞数量增加。在激发前雾化吸入沙美特罗(5毫克/毫升,持续10分钟),根据预处理与激发之间的间隔分别为0.5、1或4.5小时,可分别抑制早期渗漏26%、58%或85%。同样,沙美特罗预处理(0.05至5毫克/毫升,持续10分钟)可减少4小时时的晚期渗漏。在浓度为0.5毫克/毫升或更高时,晚期渗漏被完全阻断。预先注射β2肾上腺素能受体拮抗剂ICI-118,551可阻止这种抑制作用。沙美特罗预处理还减少了4小时时黏膜血管中中性粒细胞、嗜酸性粒细胞、单核细胞和淋巴细胞的黏附。我们得出结论,沙美特罗预处理可通过其对β2受体的作用减少抗原激发后早期和晚期反应中的血浆渗漏和白细胞黏附。