Fish J E, Jameson L S, Albright A, Norman P S
Am Rev Respir Dis. 1984 Oct;130(4):571-4. doi: 10.1164/arrd.1984.130.4.571.
Prostaglandin F2 alpha (PGF2 alpha) is generated by human lung tissue in response to a number of stimuli and is widely viewed as a bronchoconstrictor mediator. We have shown that aerosolized PGF2 alpha in concentrations between 1 and 100 micrograms/ml caused dose-related bronchoconstriction, but that continued stimulation at higher concentrations resulted in a partial return of pulmonary function toward control, suggesting that airways were refractory to further stimulation. To explore the mechanism and specificity of airway refractoriness induced by PGF2 alpha, we examined bronchomotor responses evoked by repeated PGF2 alpha stimulation, repeated histamine stimulation, and PGF2 alpha stimulation followed by histamine. Studies were carried out on 3 separate days in 7 subjects with allergic asthma. For each subject the aerosol concentration of each agonist remained constant throughout the study. Responses were measured as the percent change in FEV1 versus time, and comparisons were made between the first and second agonist challenge of each study day. We found that prior stimulation with PGF2 alpha resulted in diminished airway responsiveness, not only to PGF2 alpha but to histamine as well. In contrast, similar refractoriness could not be induced by repeated histamine stimulation, indicating that the PGF2 alpha-induced decrease in responsiveness was not a nonspecific effect of bronchoconstriction per se. Further, the finding that PGF2 alpha caused a decrease in the response to histamine suggests that diminished airway responsiveness was not due to down-regulation of specific PGF2 alpha receptors. Our findings suggest that in addition to its bronchoconstrictor properties, PGF2 alpha may play a role in the modulation of acute airway responses.
前列腺素F2α(PGF2α)由人肺组织在多种刺激下产生,被广泛视为一种支气管收缩介质。我们已经表明,浓度在1至100微克/毫升之间的雾化PGF2α会引起剂量相关的支气管收缩,但在更高浓度下持续刺激会导致肺功能部分恢复至对照水平,这表明气道对进一步刺激产生了不应性。为了探究PGF2α诱导气道不应性的机制和特异性,我们检测了重复PGF2α刺激、重复组胺刺激以及PGF2α刺激后再给予组胺所诱发的支气管运动反应。对7名过敏性哮喘患者在3个不同日期进行了研究。对于每个受试者,在整个研究过程中每种激动剂的气雾剂浓度保持恒定。反应以FEV1随时间的变化百分比来衡量,并在每个研究日的第一次和第二次激动剂激发之间进行比较。我们发现,预先用PGF2α刺激会导致气道反应性降低,不仅对PGF2α,对组胺也是如此。相比之下,重复组胺刺激不能诱导出类似的不应性,这表明PGF2α诱导的反应性降低不是支气管收缩本身的非特异性效应。此外,PGF2α导致对组胺反应降低的发现表明,气道反应性降低并非由于特定PGF2α受体的下调。我们的研究结果表明,PGF2α除了具有支气管收缩特性外,可能在急性气道反应的调节中发挥作用。