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沙美特罗和沙丁胺醇在牛气管平滑肌中对环磷酸腺苷积累与舒张作用的相关性

Correlation of cyclic AMP accumulation and relaxant actions of salmeterol and salbutamol in bovine tracheal smooth muscle.

作者信息

Ellis K E, Mistry R, Boyle J P, Challiss R A

机构信息

Department of Cell Physiology & Pharmacology, University of Leicester.

出版信息

Br J Pharmacol. 1995 Nov;116(5):2510-6. doi: 10.1111/j.1476-5381.1995.tb15103.x.

Abstract
  1. The ability of salmeterol to stimulate cyclic AMP accumulation and relaxation has been compared with that of salbutamol in bovine tracheal smooth muscle. In addition, the anti-spasmogenic effects of these agents and their abilities to modulate histamine-stimulated [3H]-inositol phosphate accumulation have also been investigated. 2. In tissue strips, a close temporal correlation was found to exist between salmeterol (0.1 microM)-induced relaxation of methacholine (500 nM)-induced tone and cyclic AMP accumulation, both maximal reversal of induced tone (26.2 +/- 6.0%) and maximal levels of cyclic AMP accumulation being achieved after 30-40 min. In contrast to salmeterol, salbutamol exerted greater and more rapid effects on both parameters. Maximal reversal of methacholine-induced tone (79.3 +/- 14.0%) and maximal levels of cyclic AMP accumulation were produced within 5 min. 3. Salmeterol-induced cyclic AMP accumulation (EC50 = 5.3 [1.8 - 15.2] nM) and inhibition of histamine (0.1 mM)-stimulated [3H]-inositol phosphate accumulation (IC50 = 1.4 [0.3-6.3] nM) were both more potent than those induced by salbutamol (EC50 = 169 [99 - 290] nM; IC50 = 13.8 [7.0 - 27.4] nM). However, maximal effects exerted by each of these agents were similar in magnitude. 4. Anti-spasmogenic effects were examined by beta-adrenoceptor agonist application to tissue strips prior to construction of spasmogen concentration-effect curves. Both salmeterol and salbutamol exerted more marked inhibition of the contractile response induced by histamine than that induced by methacholine, salmeterol being the more potent agent, while salbutamol produced a greater maximal inhibitory effect. 5. The results demonstrate that salmeterol is a more potent agent than salbutamol and have highlighted a close temporal correlation between promotion of cyclic AMP accumulation and tissue relaxation stimulated by each agent when both parameters are measured under identical conditions.
摘要
  1. 已将沙美特罗刺激环磷酸腺苷(cAMP)积聚及舒张的能力与沙丁胺醇在牛气管平滑肌中的能力进行了比较。此外,还研究了这些药物的抗痉挛作用及其调节组胺刺激的[3H] - 肌醇磷酸积聚的能力。2. 在组织条中,发现沙美特罗(0.1微摩尔/升)诱导的对乙酰甲胆碱(500纳摩尔/升)诱导的张力的舒张与cAMP积聚之间存在密切的时间相关性,诱导张力的最大逆转(26.2±6.0%)和cAMP积聚的最大水平在30 - 40分钟后达到。与沙美特罗相反,沙丁胺醇对这两个参数的作用更大且更迅速。乙酰甲胆碱诱导的张力的最大逆转(79.3±14.0%)和cAMP积聚的最大水平在5分钟内产生。3. 沙美特罗诱导的cAMP积聚(半数有效浓度[EC50]=5.3[1.8 - 15.2]纳摩尔/升)和对组胺(0.1毫摩尔/升)刺激的[3H] - 肌醇磷酸积聚的抑制作用(半数抑制浓度[IC50]=1.4[0.3 - 6.3]纳摩尔/升)均比沙丁胺醇诱导的作用更强(EC50 = 169[99 - 290]纳摩尔/升;IC50 = 13.8[7.0 - 27.4]纳摩尔/升)。然而,这些药物各自产生的最大效应在程度上相似。4. 通过在构建致痉剂浓度 - 效应曲线之前将β - 肾上腺素能受体激动剂应用于组织条来检查抗痉挛作用。沙美特罗和沙丁胺醇对组胺诱导的收缩反应的抑制作用均比对乙酰甲胆碱诱导的收缩反应更明显,沙美特罗是更有效的药物,而沙丁胺醇产生更大的最大抑制作用。5. 结果表明,沙美特罗是比沙丁胺醇更有效的药物,并突出了在相同条件下测量这两个参数时,每种药物促进cAMP积聚与组织舒张之间存在密切的时间相关性。

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