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沙丁胺醇对豚鼠离体快收缩和慢收缩肌肉收缩及环磷酸腺苷含量的影响之间的相关性。

Correlation between the effects of salbutamol on contractions and cyclic AMP content of isolated fast-and slow-contracting muscles of the guinea pig.

作者信息

Al-Jeboory A A, Marshall R J

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1978 Dec;305(3):201-6. doi: 10.1007/BF00498811.

Abstract

The effects of isoprenaline and salbutamol on incomplete tetanic contractions of the isolated soleus (slow contracting) and extensor digitorum longus (EDL-fast-contracting) muscles of the guinea pig were studied and an attempt made to correlate these effects on contractility with changes in cyclic AMP concentrations. Salbutamol was 10-12 times less potent than (+/-)isoprenaline in decreasing the force of subtetanic contractions in the soleus and between 5-6 times less potent in increasing the force of subtetanic contractions in the EDL. This observation plus the lack of activity of both the selective beta1-adrenoceptor antagonist (atenolol) and the selective beta1 agonist (H 133/22) in the EDL implies involvement of beta2-adrenoceptors in these responses of the muscles to isoprenaline and salbutamol. The soleus muscle was about 6-12 times more sensitive to effects of beta-adrenoceptor agonists than the EDL. In concentrations which produced effects on muscle contractility, salbutamol significantly elevated cyclic AMP concentrations in both types of muscle. These effects were antagonised by propranolol. It seems clear that the contrasting effects of sympathomimetic amines on slow-and fast contracting muscle are mediated through a common mechanism-elevation of cyclic AMP. Possible explanations of this apparent paradox are discussed.

摘要

研究了异丙肾上腺素和沙丁胺醇对豚鼠离体比目鱼肌(慢收缩肌)和趾长伸肌(快收缩肌,EDL)不完全强直收缩的影响,并尝试将这些对收缩性的影响与环磷酸腺苷(cAMP)浓度的变化联系起来。在降低比目鱼肌次强直收缩力方面,沙丁胺醇的效力比(±)异丙肾上腺素低10 - 12倍;在增加趾长伸肌次强直收缩力方面,沙丁胺醇的效力比异丙肾上腺素低5 - 6倍。这一观察结果,加上选择性β1肾上腺素能拮抗剂(阿替洛尔)和选择性β1激动剂(H 133/22)在趾长伸肌中均无活性,提示β2肾上腺素能受体参与了肌肉对异丙肾上腺素和沙丁胺醇的这些反应。比目鱼肌对β肾上腺素能激动剂作用的敏感性比对趾长伸肌高约6 - 12倍。在产生影响肌肉收缩性作用的浓度下,沙丁胺醇能显著提高两种类型肌肉中的环磷酸腺苷浓度。这些作用被普萘洛尔拮抗。显然,拟交感胺对慢收缩肌和快收缩肌的不同作用是通过一种共同机制——环磷酸腺苷升高介导的。讨论了这一明显矛盾现象的可能解释。

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