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福莫特罗和沙美特罗对离体人支气管的舒张作用及作用持续时间。

Relaxant effects and durations of action of formoterol and salmeterol on the isolated human bronchus.

作者信息

Naline E, Zhang Y, Qian Y, Mairon N, Anderson G P, Grandordy B, Advenier C

机构信息

Département de Pharmacologie, Faculté de Médecine, Paris, France.

出版信息

Eur Respir J. 1994 May;7(5):914-20.

PMID:7914176
Abstract

The objective of this study was to evaluate the potency and efficacy (intrinsic activity) of formoterol and salmeterol and their duration of action in comparison with other beta-adrenoceptor agonists in isolated human bronchi. Human bronchi were obtained at thoracotomy from patients with lung cancer. Potency (-log of the concentration of drug inducing 50% of maximal relaxation (-log EC50)) and efficacy (maximal effect (Emax), % of response to theophylline 3 x 10(-3) mol.l-1) were determined by analysis of cumulative isometric concentration-response curves to beta 2-adrenoceptor agonists in bronchial rings at resting tone or contracted maximally with acetylcholine 10(-3) mol.l-1 to induce functional antagonism. The onset and duration of action of beta-adrenoceptor agonists were measured by assessing the relaxant activity of drugs on the basal tone of isolated bronchi. In terms of potency, the rank order of the substances studied was formoterol > fenoterol > or = salmeterol > or = isoprenaline > or = salbutamol > or = adrenaline > or = terbutaline. Formoterol was 150-200 times more potent than isoprenaline. On preparations contracted with acetylcholine 10(-3) mol.l-1 the intrinsic activity (IA) of salbutamol, terbutaline and salmeterol compared with that of isoprenaline ranged 0.62-0.66. Intrinsic activity was higher with formoterol (0.84) and fenoterol (0.75). The onset of action of formoterol (2.14 +/- 0.55 min, n = 11) was not significantly different from that of salbutamol (1.90 +/- 0.24 min, n = 8) but shorter than that of salmeterol (6.40 +/- 1.40 min, n = 10).(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

本研究的目的是评估福莫特罗和沙美特罗的效价与效能(内在活性)及其作用持续时间,并与其他β-肾上腺素能受体激动剂在离体人支气管中的情况进行比较。肺癌患者在开胸手术时获取人支气管。通过分析支气管环对β2-肾上腺素能受体激动剂的累积等长浓度-反应曲线来确定效价(诱导最大舒张50%的药物浓度的负对数(-log EC50))和效能(最大效应(Emax),对3×10⁻³mol·L⁻¹氨茶碱反应的百分比),支气管环处于静息张力状态或用10⁻³mol·L⁻¹乙酰胆碱最大收缩以诱导功能性拮抗。通过评估药物对离体支气管基础张力的舒张活性来测量β-肾上腺素能受体激动剂的起效时间和作用持续时间。就效价而言,所研究物质的顺序为福莫特罗>非诺特罗≥沙美特罗≥异丙肾上腺素≥沙丁胺醇≥肾上腺素≥特布他林。福莫特罗的效价比异丙肾上腺素高150 - 200倍。在用10⁻³mol·L⁻¹乙酰胆碱收缩的制剂上,沙丁胺醇、特布他林和沙美特罗与异丙肾上腺素相比的内在活性(IA)为0.62 - 0.66。福莫特罗(0.84)和非诺特罗(0.75)的内在活性更高。福莫特罗的起效时间(2.14±0.55分钟,n = 11)与沙丁胺醇(1.90±0.24分钟,n = 8)无显著差异,但短于沙美特罗(6.40±1.40分钟,n = 10)。(摘要截短于250字)

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