Active sensitization discriminates between groups of calcium antagonists in lung parenchyma strips.

M Perpiñá, J Cortijo, C Sanz, J Esplugues, E J Morcillo
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Abstract

When considering the therapeutic potential of calcium antagonists in asthma, attention should be paid to the existence of marked differences among these compounds. In the present study, we have compared the effect of verapamil, diltiazem, nifedipine and trifluoperazine on contractions generated by different mechanisms (CaCl2 acting on K+ depolarized preparation, depolarization by KCl, receptor activation by acetylcholine) in lung parenchyma strips isolated from control and actively sensitized guinea-pigs. It was found that verapamil and diltiazem need higher concentrations in the sensitized specimens to elicit the same degree of inhibition obtained in controls. The reverse was found for trifluoperazine while nifedipine had an intermediate position. In conclusion, acute sensitization reveals differences between the various groups of calcium antagonists in their ability to influence agonist-induced lung parenchyma strip contraction, a finding that suggests that these drugs may also behave diversely in the clinical setting.

肺实质条中钙拮抗剂的活性致敏区分。
在考虑钙拮抗剂对哮喘的治疗潜力时,应注意这些化合物之间存在显着差异。在本研究中,我们比较了维拉帕米、地尔硫卓、硝苯地平和三氟哌嗪对对照和主动致敏豚鼠肺实质条不同机制(CaCl2作用于K+去极化制剂、KCl去极化、乙酰胆碱激活受体)产生的收缩的影响。发现维拉帕米和地尔硫卓在致敏标本中需要更高的浓度才能引起与对照组相同程度的抑制。三氟拉嗪的作用正好相反,硝苯地平则处于中间位置。总之,急性致敏揭示了不同钙拮抗剂组对激动剂诱导的肺实质条形收缩的影响能力的差异,这一发现表明这些药物在临床环境中也可能表现不同。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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