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章鱼胺和儿茶酚胺对大鼠大脑皮层单个神经元作用的比较。

Comparison of the actions of octopamine and catecholamines on single neurones of the rat cerebral cortex.

作者信息

Hicks T P, McLennan H

出版信息

Br J Pharmacol. 1978 Dec;64(4):485-91. doi: 10.1111/j.1476-5381.1978.tb17309.x.

Abstract
  1. The technique of microelectrophoresis was used to compare the actions of octopamine, noradrenaline and dopamine on single cortical neurones of the rat. 2. Octopamine both excited and depressed neurones of the cortex. Frequently cells depressed by noradrenaline were excited by octopamine; occasionally the converse was true. The time courses of action of the two amines also differed. Dopamine-elicited excitations were observed, but also were not correlated with octopamine-elicited effects. 3. When octopamine and noradrenaline both caused depressant effects, octopamine frequently was of less apparent potency than noradrenaline. When these amines were excitatory, octopamine appeared at least as and sometimes more potent than noradrenaline. 4. Octopamine was only weakly effective on cortical neurones identified by antidromic stimulation of the pyramidal tract, or synaptically excited by stimulation of the ventrobasal thalamus. 5. alpha-Flupenthixol and propranolol were without effect on octopamine-elicited changes in firing rate at doses which were effective in blocking the actions of dopamine and noradrenaline respectively. Metoclopramide did not block the actions of any of the three agonists, but had strong effects of its own. 6. The results suggest that receptors sensitive to octopamine, and which appear to be pharmacologically distinct from those previously categorized as noradrenaline and dopamine receptors, may exist on central neurones of the rat.
摘要
  1. 运用微电泳技术比较了章鱼胺、去甲肾上腺素和多巴胺对大鼠单个皮层神经元的作用。2. 章鱼胺既能兴奋也能抑制皮层神经元。通常被去甲肾上腺素抑制的细胞会被章鱼胺兴奋;偶尔情况相反。这两种胺的作用时间进程也不同。观察到多巴胺引起的兴奋,但也与章鱼胺引起的效应无关。3. 当章鱼胺和去甲肾上腺素都产生抑制作用时,章鱼胺的效力通常比去甲肾上腺素弱。当这些胺具有兴奋作用时,章鱼胺至少与去甲肾上腺素一样有效,有时甚至更有效。4. 章鱼胺对通过锥体束逆行刺激鉴定的皮层神经元或通过腹侧基底丘脑刺激突触兴奋的皮层神经元只有微弱的作用。5. 在分别有效阻断多巴胺和去甲肾上腺素作用的剂量下,α-氟哌噻吨和普萘洛尔对章鱼胺引起的放电频率变化没有影响。甲氧氯普胺不阻断这三种激动剂中的任何一种的作用,但自身有很强的作用。6. 结果表明,大鼠中枢神经元上可能存在对章鱼胺敏感的受体,且这些受体在药理学上似乎与先前归类为去甲肾上腺素和多巴胺受体的受体不同。

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