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多巴胺对体外培养海马神经元的兴奋和抑制作用。D2和D1受体的参与。

Excitatory and inhibitory action of dopamine on hippocampal neurons in vitro. Involvement of D2 and D1 receptors.

作者信息

Smiałowski A, Bijak M

机构信息

Polish Academy of Sciences, Institute of Pharmacology, Kraków, Poland.

出版信息

Neuroscience. 1987 Oct;23(1):95-101. doi: 10.1016/0306-4522(87)90274-0.

Abstract

The study examined the effects of dopaminergic agonists on the extracellularly recorded spontaneous activity of CA1 neurons in hippocampal slices of the rat. Dopamine evoked excitation or inhibition of the neuronal firing rate, the first reaction being more sensitive to the substance. Having used selective dopaminergic agonists (pergolide and 2,3,4,5-tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepines) and selective antagonists (haloperidol, spiperone, sulpiride and (R)-(+)-8-chloro-2,3,4,5-tetrahydro-3-methyl-5-phenyl-1H-3- benzazepine-7-ol), it was concluded that the excitation evoked by dopamine was due to activation of D2 dopamine receptors, while the inhibition was the result of D1 receptor activation. The effects of the dopamine agonists on the firing of CA1 neurons were long-lasting, which suggests a modulating role of dopamine in the hippocampus.

摘要

该研究检测了多巴胺能激动剂对大鼠海马切片中细胞外记录的CA1神经元自发活动的影响。多巴胺可诱发神经元放电频率的兴奋或抑制,其中首次反应对该物质更为敏感。使用选择性多巴胺能激动剂(培高利特和2,3,4,5-四氢-7,8-二羟基-1-苯基-1H-3-苯并氮杂卓)和选择性拮抗剂(氟哌啶醇、螺哌隆、舒必利和(R)-(+)-8-氯-2,3,4,5-四氢-3-甲基-5-苯基-1H-3-苯并氮杂卓-7-醇)后得出结论,多巴胺诱发的兴奋是由于D2多巴胺受体的激活,而抑制是D1受体激活的结果。多巴胺激动剂对CA1神经元放电的影响具有持久性,这表明多巴胺在海马体中具有调节作用。

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