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心得舒的局部麻醉和抗心律失常作用与其对离体心肌细胞内电位及其他特性的影响

Local anaesthetic and anti-arrhythmic actions of alprenolol relative to its effect on intracellular potentials and other properties of isolated cardiac muscle.

作者信息

Singh B N, Williams E M

出版信息

Br J Pharmacol. 1970 Apr;38(4):749-57. doi: 10.1111/j.1476-5381.1970.tb09884.x.

Abstract
  1. Alprenolol, a beta-adrenoceptor blocking drug reported to have the same potency as propranolol in vitro and in vivo, was found to be four times more active than procaine as a local anaesthetic on frog sciatic nerve.2. At doses of 0.125 mg/kg and above alprenolol protected anaesthetized guinea-pigs against ouabain-induced ventricular fibrillation.3. In isolated rabbit atria, resting potentials were unchanged, and the duration of the action potential was not prolonged, by concentrations of alprenolol up to 10.5 x 10(-6)M. The maximum rate of depolarization (MRD), however, was reduced by 30% at a concentration of 0.525 x 10(-6)M. This was 214 times less than the concentration which reduced the frog action potential height by 25%.4. The concentration of alprenolol required to produce more than 15% decrease in contraction or maximum driven frequency was 3.5 x 10(-6)M.5. As a test of the direct action of alprenolol on isolated cardiac muscle, MRD was also a more sensitive test than the measurement of electrical threshold or conduction velocity.
摘要
  1. 阿普洛尔是一种β-肾上腺素能受体阻断药,据报道其在体外和体内的效力与普萘洛尔相同,在青蛙坐骨神经上作为局部麻醉剂时,发现其活性比普鲁卡因高四倍。

  2. 剂量在0.125毫克/千克及以上时,阿普洛尔可保护麻醉的豚鼠免受哇巴因诱导的心室颤动。

  3. 在离体兔心房中,浓度高达10.5×10⁻⁶M的阿普洛尔不会改变静息电位,也不会延长动作电位的持续时间。然而,在浓度为0.525×10⁻⁶M时,最大去极化速率(MRD)降低了30%。这比使青蛙动作电位高度降低25%的浓度低214倍。

  4. 使收缩或最大驱动频率降低超过15%所需的阿普洛尔浓度为3.5×10⁻⁶M。

  5. 作为阿普洛尔对离体心肌直接作用的测试,最大去极化速率也是比电阈值或传导速度测量更敏感的测试。

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Antiarrhythmic drug research.抗心律失常药物研究。
Br J Pharmacol. 2006 Jan;147 Suppl 1(Suppl 1):S222-31. doi: 10.1038/sj.bjp.0706500.

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