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微量电泳施加的(3,4 - 二羟基 - 苯氨基)-2 - 咪唑啉(DPI)对单个皮层神经元的作用。

The action of microelectrophoretically applied (3,4-dihydroxy-phenylamino)-2-imidazoline (DPI) on single cortical neurones.

作者信息

Bevan P, Bradshaw C M, Pun R Y, Slater N T, Szabadi E

出版信息

Br J Pharmacol. 1979 Apr;65(4):701-6. doi: 10.1111/j.1476-5381.1979.tb07884.x.

Abstract
  1. The technique of microelectrophoresis was used in order to compare the actions of the imidazoline derivative, (3,4-dihydroxy-phenylamino)-2-imidazoline (DPI), with those of dopamine and phenylephrine on single neurones in the cerebral cortex of the rat anaesthetized with halothane. 2. DPI and phenylephrine were almost exclusively excitatory, whereas dopamine could evoke both excitatory and depressant responses. 3. In the case of excitatory responses, DPI appeared to be more potent than dopamine, and was approximately equipotent with phenylephrine. 4. The dopamine antagonist, haloperidol, could discriminate between excitatory responses to DPI and dopamine: responses to dopamine were abolished, whereas responses to DPI, and to a control agonist, acetylcholine, were unaffected. 5. The alpha-adrenoceptor antagonist, phenoxybenzamine, antagonized equally excitatory responses to DPI and phenylephrine. Responses to acetylcholine were not affected. 6. It is concluded that DPI does not stimulate dopamine receptors on cortical neurones; the excitatory responses of these cells to DPI may be mediated by alpha-adrenoceptors.
摘要
  1. 采用微电泳技术,以便比较咪唑啉衍生物(3,4-二羟基苯氨基)-2-咪唑啉(DPI)与多巴胺及去氧肾上腺素对用氟烷麻醉的大鼠大脑皮质单个神经元的作用。2. DPI和去氧肾上腺素几乎完全是兴奋性的,而多巴胺既能引起兴奋反应,也能引起抑制反应。3. 就兴奋反应而言,DPI似乎比多巴胺更有效,且与去氧肾上腺素大致等效。4. 多巴胺拮抗剂氟哌啶醇能够区分对DPI和多巴胺的兴奋反应:对多巴胺的反应被消除,而对DPI以及对照激动剂乙酰胆碱的反应未受影响。5. α-肾上腺素能受体拮抗剂酚苄明同等程度地拮抗对DPI和去氧肾上腺素的兴奋反应。对乙酰胆碱的反应未受影响。6. 得出结论:DPI不刺激皮质神经元上的多巴胺受体;这些细胞对DPI的兴奋反应可能由α-肾上腺素能受体介导。

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