Phillips G D, Bagga P K, Djukanovic R, Holgate S T
Immunopharmacology Group, Southampton General Hospital, United Kingdom.
Am Rev Respir Dis. 1989 Aug;140(2):321-6. doi: 10.1164/ajrccm/140.2.321.
Repeated bronchoprovocation with adenosine 5'-monophosphate (AMP) in atopic, nonasthmatic subjects produces a state of refractoriness to the nucleotide that may be due either to depletion of preformed mediators from airway mast cells or down-regulation of purinoceptors on the surface of these cells. To investigate this further, we compared the effect on immediate allergen-provoked bronchoconstriction of preceding repeated challenges with histamine and AMP in eight atopic, mildly asthmatic subjects. In three successive AMP concentration-response studies, the geometric mean PC20 AMP increased from 275.3 to 1154.3 (p less than 0.01) and 1976.7 (p less than 0.01) mg/ml, respectively, whereas no significant similar increase in PC20 occurred with repeated histamine challenges. Refractoriness to AMP was not associated with any significant decrease in airways responsiveness to histamine. When compared with the response after repeated provocation with inhaled histamine, repeated exposure of the airways to AMP potentiated, rather than inhibited, immediate allergen-induced bronchoconstriction by a mean 57 +/- 22.6% (p less than 0.05) when the data were expressed as the area under the FEV1-time response curve. The ability of airways that have been rendered less responsive to inhaled AMP to exhibit an increased response to allergen suggests that tachyphylaxis to AMP is unlikely to be caused by depletion of preformed mast cell-derived mediators such as histamine.
在特应性非哮喘受试者中,用5'-单磷酸腺苷(AMP)反复进行支气管激发试验会产生对该核苷酸的不应性状态,这可能是由于气道肥大细胞中预先形成的介质耗竭,或者是这些细胞表面嘌呤受体的下调所致。为了进一步研究这一点,我们比较了在8名特应性轻度哮喘受试者中,组胺和AMP预先反复激发对即刻变应原诱发支气管收缩的影响。在三项连续的AMP浓度-反应研究中,几何平均PC20 AMP分别从275.3增加到1154.3(p<0.01)和1976.7(p<0.01)mg/ml,而反复组胺激发时PC20没有类似的显著增加。对AMP的不应性与气道对组胺反应性的任何显著降低均无关。当与吸入组胺反复激发后的反应相比时,气道反复暴露于AMP后,以FEV1-时间反应曲线下面积表示数据时,即刻变应原诱发的支气管收缩平均增强了57±22.6%(p<0.05),而不是受到抑制。气道对吸入AMP反应性降低后对变应原表现出增强反应的能力表明,对AMP的快速耐受不太可能是由组胺等预先形成的肥大细胞衍生介质耗竭引起的。