外周肾上腺素能受体介导的大鼠运动活性降低。

J M O'Donnell
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引用次数: 0

摘要

非选择性肾上腺素能激动剂异丙肾上腺素、β -2选择性激动剂克仑特罗以及β -1选择性激动剂多巴酚丁胺和丙戊醇在较小程度上以剂量依赖性方式降低大鼠的运动活性。这些作用可被肾上腺素能拮抗剂心得安拮抗,提示是由肾上腺素能受体介导的。亲水性β -肾上腺素能拮抗剂CGP-12177通过血脑屏障的能力较差,也能阻断盐酸克仑特罗对运动活性的影响,其作用类似于心得安,提示刺激外周β -肾上腺素能受体足以降低运动活性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Reduced locomotor activity of rats mediated by peripheral beta adrenergic receptors.

The nonselective beta adrenergic agonist isoproterenol, the beta-2 selective agonist clenbuterol and, to a lesser extent, the beta-1 selective agonists dobutamine and prenalterol reduced locomotor activity of rats in a dose-dependent manner. These effects were antagonized by the beta adrenergic antagonist propranolol, suggesting mediation by beta adrenergic receptors. The hydrophilic beta adrenergic antagonist CGP-12177, which crosses the blood-brain barrier poorly, also blocked the effect of clenbuterol on locomotor activity with a potency similar to propranolol, suggesting that stimulation of peripheral beta adrenergic receptors is sufficient for reducing locomotor activity.

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