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大鼠纹状体切片放射性标记多巴胺与内源性多巴胺释放的比较:电场刺激的影响及D2自受体的调节作用

Comparison between radiolabelled and endogenous dopamine release from rat striatal slices: effects of electrical field stimulation and regulation by D2-autoreceptors.

作者信息

Herdon H, Nahorski S R

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1987 Mar;335(3):238-42. doi: 10.1007/BF00172790.

DOI:10.1007/BF00172790
PMID:3587370
Abstract

Direct comparisons have been made between the release of radiolabelled and endogenous dopamine from superfused rat striatal slices prelabelled with 3H-dopamine. Both spontaneous release and release evoked by electrical field stimulation (3 Hz, 2 min) were measured using a high-sensitivity HPLC system with electrochemical (coulometric) detection, plus scintillation counting of chromatographically separated superfusate fractions. Two periods of electrical stimulation released similar amounts of endogenous dopamine, but the second stimulation released much less 3H-dopamine than did the first, although the levels of spontaneous release immediately before the two stimuli were similar. Substantial increases in endogenous 3,4-dihydroxy phenyl acetic acid (DOPAC) release but only minor increases in 3H-DOPAC release occurred following the two stimuli. The dopamine agonist pergolide (1 microM) reduced the electrically-stimulated release of both 3H-dopamine and endogenous dopamine to a similar extent, whilst the D2-selective antagonist sulpiride (1 microM) produced large increases in both 3H-dopamine and endogenous dopamine electrically-stimulated release. In addition, spontaneous release of both 3H-dopamine and endogenous dopamine were decreased by pergolide and increased by sulpiride. Co-addition of sulpiride and pergolide produced lesser increases than those seen with sulpiride alone. These studies indicate that, despite major differences between 3H-dopamine and endogenous dopamine release in response to various stimuli, their regulation by D2-autoreceptors appears similar; a novel finding being the modulation of spontaneous 3H-dopamine release by autoreceptors.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

已对用3H-多巴胺预标记的大鼠纹状体切片灌流液中放射性标记多巴胺和内源性多巴胺的释放进行了直接比较。使用具有电化学(电量分析)检测功能的高灵敏度高效液相色谱系统,外加对色谱分离的灌流液组分进行闪烁计数,来测量自发释放以及电场刺激(3赫兹,2分钟)诱发的释放。两段电刺激释放的内源性多巴胺量相似,但第二次刺激释放的3H-多巴胺比第一次少得多,尽管两次刺激前的自发释放水平相似。两次刺激后,内源性3,4-二羟基苯乙酸(DOPAC)释放大幅增加,但3H-DOPAC释放仅略有增加。多巴胺激动剂培高利特(1微摩尔)在相似程度上降低了3H-多巴胺和内源性多巴胺的电刺激释放,而D2选择性拮抗剂舒必利(1微摩尔)则使3H-多巴胺和内源性多巴胺的电刺激释放大幅增加。此外,培高利特降低了3H-多巴胺和内源性多巴胺的自发释放,舒必利则增加了它们的自发释放。舒必利和培高利特共同添加时产生的增加幅度小于单独使用舒必利时。这些研究表明,尽管3H-多巴胺和内源性多巴胺在对各种刺激的释放方面存在重大差异,但它们受D2自身受体的调节似乎相似;一个新发现是自身受体对3H-多巴胺自发释放的调节。(摘要截短于250字)

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Investigations of the roles of dihydropyridine and omega-conotoxin-sensitive calcium channels in mediating depolarisation-evoked endogenous dopamine release from striatal slices.二氢吡啶和ω-芋螺毒素敏感性钙通道在介导纹状体切片去极化诱发内源性多巴胺释放中的作用研究。
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In vitro effect of the racemic mixture and the (-)enantiomer of N-n-propyl-3-(3-hydroxyphenyl)-piperidine (3-PPP) on postsynaptic dopamine receptors and on a presynaptic dopamine autoreceptor.消旋混合物及N-正丙基-3-(3-羟基苯基)-哌啶(3-PPP)的(-)对映体对突触后多巴胺受体及突触前多巴胺自身受体的体外作用
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Presynaptic regulation of the release of catecholamines.儿茶酚胺释放的突触前调节。
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Presynaptic receptors.突触前受体
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Behavioral properties of GBR 12909, GBR 13069 and GBR 13098: specific inhibitors of dopamine uptake.GBR 12909、GBR 13069和GBR 13098的行为特性:多巴胺摄取的特异性抑制剂。
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