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阿扑吗啡对脑5-羟色胺更新率的影响。

Influence of apomorphine on brain serotonin turnover rate.

作者信息

Grabowska M

出版信息

Pharmacol Biochem Behav. 1975 Jul-Aug;3(4):589-91. doi: 10.1016/0091-3057(75)90178-1.

DOI:10.1016/0091-3057(75)90178-1
PMID:1187722
Abstract

Apomorphine (5.0 mg/kg) accelerated the disappearance of 5-HIAA from the brain of pargylinepretreated rats as well as depletion of brain 5-HT caused by inhibition of its synthesis. The latter effect has been abolished by spiroperidol. The results obtained suggest that apomorphine increases the 5-HT turnover rate, secondary to the stimulation of central dopamine receptors.

摘要

阿扑吗啡(5.0毫克/千克)加速了帕吉林预处理大鼠脑中5-羟吲哚乙酸(5-HIAA)的消失以及因5-羟色胺(5-HT)合成受抑制而导致的脑内5-HT耗竭。后一种效应已被螺哌啶醇消除。所得结果表明,阿扑吗啡通过刺激中枢多巴胺受体,继发增加了5-HT的周转速率。

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Influence of apomorphine on brain serotonin turnover rate.阿扑吗啡对脑5-羟色胺更新率的影响。
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引用本文的文献

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Pharmacological Insights into the Use of Apomorphine in Parkinson's Disease: Clinical Relevance.阿扑吗啡在帕金森病中的应用的药理学研究进展:临床相关性。
Clin Drug Investig. 2018 Apr;38(4):287-312. doi: 10.1007/s40261-018-0619-3.
2
5,7-Dihydroxytryptamine lesions of the amygdala reduce amphetamine- and apomorphine-induced stereotyped behaviour in the rat.杏仁核的5,7-二羟基色胺损伤可减少大鼠中苯丙胺和阿扑吗啡诱导的刻板行为。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Jul;312(3):235-8. doi: 10.1007/BF00499152.
3
Apomorphine in the rat nucleus accumbens: effects on the synthesis of 5-hydroxytryptamine and noradrenaline, the motor activity and the body temperature.
阿扑吗啡对大鼠伏隔核的作用:对5-羟色胺和去甲肾上腺素合成、运动活性及体温的影响。
J Neural Transm. 1976;38(1):1-8. doi: 10.1007/BF01254135.
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Effect of nomifensine on central 5-hydroxytryptamine neurons.去甲丙咪嗪对中枢5-羟色胺能神经元的作用。
J Neural Transm. 1977;40(3):195-204. doi: 10.1007/BF01300134.
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Dopamine agonists and interaction with other neurotransmitter systems.多巴胺激动剂及其与其他神经递质系统的相互作用。
Naunyn Schmiedebergs Arch Pharmacol. 1977;297 Suppl 1:S53-4. doi: 10.1007/BF00587777.
6
Possible importance of 5-hydroxytryptamine in neuroleptic-induced catalepsy in rats [proceedings].5-羟色胺在大鼠抗精神病药物诱发的僵住症中的潜在重要性[会议论文集]
Br J Pharmacol. 1977 Jun;60(2):267P-268P.
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