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某些拟交感神经支气管扩张剂和β-肾上腺素能受体阻断药物对猫比目鱼肌收缩的作用。

Actions of some sympathomimetic bronchodilator and beta-adrenoceptor blocking drugs on contractions of the cat soleus muscle.

作者信息

Bowman W C, Nott M W

出版信息

Br J Pharmacol. 1970 Jan;38(1):37-49. doi: 10.1111/j.1476-5381.1970.tb10334.x.

Abstract
  1. (-)-Isoprenaline, salbutamol, orciprenaline and quinterenol injected intravenously decreased the tension and degree of fusion of incomplete tetanic contractions of the soleus muscle of the anaesthetized cat.2. Under the most sensitive conditions, the smallest effective dose of (-)-isoprenaline was of the order of 0.01 mug/kg intravenously. Salbutamol was usually 6-10 times, orciprenaline 20-30 times and quinterenol about 35 times less potent than isoprenaline. The effects of salbutamol were about 1.6 times, of orciprenaline about 1.8 times and of quinterenol more than 20 times as long lasting as those of (-)-isoprenaline.3. The effects of the sympathomimetic amines were blocked by propranolol, H56/28, H35/25 and butoxamine but not by ICI 50172. The combined results with agonists and antagonists indicate that the receptors involved can be classified as of the beta(2) type.4. The effect of the amines on the cat soleus muscle appears to be analogous to that causing enhancement of physiological tremor in man, which suggests that skeletal muscle tremor may be an occasional unwanted side effect of the use of these bronchodilators.
摘要
  1. 静脉注射(-)-异丙肾上腺素、沙丁胺醇、奥西那林和喹丁醇可降低麻醉猫比目鱼肌不完全强直收缩的张力和融合程度。

  2. 在最敏感的条件下,(-)-异丙肾上腺素的最小有效静脉注射剂量约为0.01微克/千克。沙丁胺醇的效力通常比异丙肾上腺素低6 - 10倍,奥西那林低20 - 30倍,喹丁醇低约35倍。沙丁胺醇的作用持续时间约为(-)-异丙肾上腺素的1.6倍,奥西那林约为1.8倍,喹丁醇超过20倍。

  3. 拟交感胺的作用被普萘洛尔、H56/28、H35/25和丁氧胺阻断,但不被ICI 50172阻断。激动剂和拮抗剂的联合结果表明,所涉及的受体可归类为β₂型。

  4. 胺类对猫比目鱼肌的作用似乎类似于导致人类生理性震颤增强的作用,这表明骨骼肌震颤可能是使用这些支气管扩张剂时偶尔出现的不良副作用。

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Adrenaline and slow-contracting skeletal muscles.
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