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放射性标记的β-肾上腺素能受体阻断剂在大鼠离体输精管中的摄取与溢出

The uptake and overflow of radiolabelled beta-adrenoceptor blocking agents by the isolated vas deferens of the rat.

作者信息

Lewis M J

出版信息

Br J Pharmacol. 1977 Aug;60(4):595-600. doi: 10.1111/j.1476-5381.1977.tb07540.x.

Abstract
  1. A comparison of uptake into and overflow from the isolated vas deferens of the rat has been made between [3H]-noradrenaline ([3H]-NA), [14C]-D-sorbitol and three radio-labelled beta-adrenoceptor blocking agents, [14C]-practolol, [14C]-(+/-)-propranolol and [3H]-penbutolol. 2. The accumulation of [3H]-NA after 30 min incubation was reduced by desmethylimipramine (DMI) 1 X 10(-8)M and was also reduced in vasa from rats pretreated with 6-hydroxydopamine (6-OHDA). This was not so with [14C]-D-sorbitol. 3. 6-OHDA pretreatment of the rats reduced the uptake of [3H]-penbutolol after 30 min incubation but not that of [4C]-propranolol or [14C]-practolol. DMI 1 X 10(-8)M did not alter the tissue uptake of [14C]-propranolol, [14C]-practolol or [3H]-penbutolol. 4. Electrical stimulation of vasa preloaded with [3H]-NA caused a significantly greater increase in [3H]-NA overflow than during the resting, unstimulated periods. No such increase in overflow was observed with [14C]-sorbitol or any of the three beta-adrenoceptor blocking agents use. 5. The beta-adrenoceptor blocking agent penbutolol was shown to possess adrenergic neurone blocking activity in the isolated vas deferens of the rat. 6. It is concluded that any effect that practolol or (+/-)-propranolol have on noradrenergic neurones is brought about without the need for these drugs to gain access to the interior of the neurone.
摘要
  1. 对大鼠离体输精管中[3H]-去甲肾上腺素([3H]-NA)、[14C]-D-山梨醇以及三种放射性标记的β-肾上腺素能受体阻滞剂[14C]-普拉洛尔、[14C]-(±)-普萘洛尔和[3H]-喷布洛尔的摄取和溢出情况进行了比较。2. 孵育30分钟后,1×10(-8)M去甲丙咪嗪(DMI)可降低[3H]-NA的蓄积,用6-羟基多巴胺(6-OHDA)预处理大鼠后的输精管中[3H]-NA蓄积也减少。[14C]-D-山梨醇的情况并非如此。3. 用6-OHDA预处理大鼠后,孵育30分钟可降低[3H]-喷布洛尔的摄取,但不影响[4C]-普萘洛尔或[14C]-普拉洛尔的摄取。1×10(-8)M的DMI不会改变[14C]-普萘洛尔、[14C]-普拉洛尔或[3H]-喷布洛尔的组织摄取。4. 对预先加载[3H]-NA的输精管进行电刺激,导致[3H]-NA溢出的增加显著大于静息、未刺激期。用[14C]-山梨醇或所使用的三种β-肾上腺素能受体阻滞剂中的任何一种均未观察到这种溢出增加。5. 已证明β-肾上腺素能受体阻滞剂喷布洛尔在大鼠离体输精管中具有肾上腺素能神经元阻滞活性。6. 得出的结论是,普拉洛尔或(±)-普萘洛尔对去甲肾上腺素能神经元的任何作用都是在这些药物无需进入神经元内部的情况下产生的。

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