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大鼠伏隔核神经元的药理学研究。

Studies on the pharmacology of neurones in the nucleus accumbens of the rat.

作者信息

Woodruff G N, McCarthy P S, Walker R J

出版信息

Brain Res. 1976 Oct 15;115(2):233-42. doi: 10.1016/0006-8993(76)90509-6.

Abstract

A study was made of the effects of iontophoretically applied drugs on single neurones in the nucleus accumgens and caudate nucleus of rats anaesthetized with urethane. Neurones in the caudate nucleus were inhibited by dopamine, dibutyryl cyclic AMP, ADTN and ergometrine. Acetylcholine and homocysteic acid caused excitation of striatal neurones. In the nucleus accumbens neurones were inhibited by dopamine, ADTN, ergometrine, dibutyryl cyclic AMP, glycine and gamma-aminobutyric acid. The responses of glycine and gamma-aminobutyric acid were antagonised by strychnine and picrotoxin, respectively. Acetylcholine and homocysteic acid caused excitation of neurones in the nucleus acumbens; the effects of acetylcholine were blocked by atropine. The results are consistent with the suggestion that dopamine is an inhibitory transmitter in the nucleus accumbens and in the caudate nucleus and support the hypothesis that the effects of dopamine are mediated by cyclic AMP. The locomotor stimulants ADTN and ergometrine mimicked the inhibitory actions of dopamine in both the striatum and in the nucleus accumbens. These results support the suggestion that dopamine receptors in the nucleus accumbens are involved in the actions of locomotor stimulant drugs.

摘要

研究了离子电渗法施加药物对氨基甲酸乙酯麻醉的大鼠伏隔核和尾状核中单神经元的影响。尾状核中的神经元受到多巴胺、二丁酰环磷酸腺苷、ADTN和麦角新碱的抑制。乙酰胆碱和高胱氨酸引起纹状体神经元兴奋。在伏隔核中,神经元受到多巴胺、ADTN、麦角新碱、二丁酰环磷酸腺苷、甘氨酸和γ-氨基丁酸的抑制。甘氨酸和γ-氨基丁酸的反应分别被士的宁和印防己毒素拮抗。乙酰胆碱和高胱氨酸引起伏隔核中神经元兴奋;乙酰胆碱的作用被阿托品阻断。结果与多巴胺是伏隔核和尾状核中的抑制性递质这一观点一致,并支持多巴胺的作用由环磷酸腺苷介导的假说。运动兴奋剂ADTN和麦角新碱在纹状体和伏隔核中模拟了多巴胺的抑制作用。这些结果支持伏隔核中的多巴胺受体参与运动兴奋剂药物作用的观点。

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