首页> 美国卫生研究院文献>British Journal of Pharmacology and Chemotherapy >Effects of beta 2-adrenoceptor agonists on anti-IgE-induced contraction and smooth muscle reactivity in human airways.
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Effects of beta 2-adrenoceptor agonists on anti-IgE-induced contraction and smooth muscle reactivity in human airways.

机译:β2肾上腺素受体激动剂对人呼吸道中抗IgE诱导的收缩和平滑肌反应性的影响。

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摘要

1. The beta 2-adrenoceptor agonists, salbutamol, salmeterol and RP 58802 relaxed basal tone of human isolated bronchial smooth muscle. Salmeterol- and RP 58802-induced relaxations persisted for more than 4 h when the medium was constantly renewed after treatment. 2. Salbutamol, salmeterol and RP 58802 reversed histamine-induced contractions in human airways (pD2 values: 6.15 +/- 0.21, 6.00 +/- 0.19 and 6.56 +/- 0.12, respectively). 3. Anti-IgE-induced contractions were significantly inhibited immediately after pretreatment of preparations with beta 2-adrenoceptor agonists (10 microM). However, when tissues were treated with beta 2-agonists and then washed for a period of 4 h, salmeterol was the only agonist which significantly inhibited the anti-IgE response. 4. Histamine response curves were shifted to the right immediately after pretreatment of tissues with the beta 2-adrenoceptor agonists (10 microM; 20 min), but maximal contractions were not affected. After a 4 h washing period, the histamine curves were not significantly different from controls. Concentration-effect curves to acetylcholine (ACh) or leukotriene C4 (LTC4) were not significantly modified after beta 2-agonist pretreatment. 5. These results suggest that beta 2-adrenoceptor agonists may prevent anti-IgE-induced contraction by inhibition of mediator release rather than alterations of those mechanisms involved in airway smooth muscle contraction.
机译:1.β2肾上腺素受体激动剂沙丁胺醇,沙美特罗和RP 58802可以减轻人分离的支气管平滑肌的基础张力。当处理后不断更新培养基时,沙美特罗和RP 58802诱导的松弛持续超过4小时。 2.沙丁胺醇,沙美特罗和RP 58802逆转了组胺诱导的人类气道收缩(pD2值:分别为6.15 +/- 0.21、6.00 +/- 0.19和6.56 +/- 0.12)。 3.用β2肾上腺素受体激动剂(10 microM)对制剂进行预处理后,抗IgE诱导的收缩立即受到明显抑制。但是,当用β2-激动剂处理组织然后清洗4小时时,沙美特罗是唯一能显着抑制抗IgE反应的激动剂。 4.用β2肾上腺素受体激动剂(10 microM; 20分钟)对组织进行预处理后,组胺反应曲线立即向右移动,但最大收缩不受影响。洗涤4小时后,组胺曲线与对照无显着差异。 β2-激动剂预处理后,对乙酰胆碱(ACh)或白三烯C4(LTC4)的浓度-效应曲线没有明显改变。 5.这些结果表明,β2肾上腺素受体激动剂可能通过抑制介质释放而不是改变与气道平滑肌收缩有关的机制而阻止抗IgE诱导的收缩。

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