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Quipazine: its effects on rat brain 5-hydroxytryptamine metabolism, monoamine oxidase activity and behaviour.

作者信息

Green A R, Youdim M B, Grahame-Smith D G

出版信息

Neuropharmacology. 1976 Mar;15(3):173-9. doi: 10.1016/0028-3908(76)90026-5.

DOI:10.1016/0028-3908(76)90026-5
PMID:132619
Abstract
摘要

相似文献

1
Quipazine: its effects on rat brain 5-hydroxytryptamine metabolism, monoamine oxidase activity and behaviour.喹哌嗪:其对大鼠脑5-羟色胺代谢、单胺氧化酶活性及行为的影响。
Neuropharmacology. 1976 Mar;15(3):173-9. doi: 10.1016/0028-3908(76)90026-5.
2
Evidence for dopamine deamination by both type A and type B monoamine oxidase in rat brain in vivo and for the degree of inhibition of enzyme necessary for increased functional activity of dopamine and 5-hydroxytryptamine.大鼠脑内A型和B型单胺氧化酶对多巴胺脱氨基作用的体内证据,以及多巴胺和5-羟色胺功能活性增强所需的酶抑制程度。
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3
The heterogeneity of monoamine oxidase in distinct populations of rat brain mitochondria.
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4
Effect of selective monoamine oxidase inhibitors on rat brain mitochondrial monoamine oxidase during hyperbaric oxygenation.高压氧治疗期间选择性单胺氧化酶抑制剂对大鼠脑线粒体单胺氧化酶的影响。
Commun Psychopharmacol. 1977;1(1):39-47.
5
Developmental changes in the activity and substrate specificities of mouse brain monoamine oxidase.小鼠脑单胺氧化酶活性及底物特异性的发育变化
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6
5-hydroxytryptamine catabolism in the rat brain during ontogenesis.大鼠脑在个体发育过程中的5-羟色胺分解代谢
J Neurochem. 1977 Feb;28(2):415-22. doi: 10.1111/j.1471-4159.1977.tb07763.x.
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Inhibition of central monoamine oxidase by imidazoline2 site-selective ligands.
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The effects of quipazine on serotonin metabolism in rat brain.喹哌嗪对大鼠脑内5-羟色胺代谢的影响。
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Inhibition by clorgyline and deprenyl of the different forms of monoamine oxidase in rat liver mitochondria.氯吉兰和司来吉兰对大鼠肝线粒体中不同形式单胺氧化酶的抑制作用。
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Potentiation of 3,4-methylenedioxymethamphetamine-induced 5-HT release in the rat substantia nigra by clorgyline, a monoamine oxidase A inhibitor.单胺氧化酶A抑制剂氯吉兰增强3,4-亚甲基二氧甲基苯丙胺诱导的大鼠黑质5-羟色胺释放
Clin Exp Pharmacol Physiol. 2007 Oct;34(10):1051-7. doi: 10.1111/j.1440-1681.2007.04734.x.

引用本文的文献

1
Antagonism of 5-hydroxytryptamine receptors by quipazine.喹哌嗪对5-羟色胺受体的拮抗作用。
Br J Pharmacol. 1980 Mar;68(3):525-32. doi: 10.1111/j.1476-5381.1980.tb14568.x.
2
Methysergide blocks the sleep suppressant action of quipazine in rats.甲基麦角新碱可阻断喹哌嗪对大鼠的睡眠抑制作用。
Psychopharmacology (Berl). 1982;76(3):255-9. doi: 10.1007/BF00432556.
3
Repeated administration of subconvulsant doses of GABA antagonist drugs. II. Effect on monoamine-mediated behaviour.重复给予亚惊厥剂量的γ-氨基丁酸(GABA)拮抗剂药物。II. 对单胺介导行为的影响。
Psychopharmacology (Berl). 1982;76(1):88-91. doi: 10.1007/BF00430763.
4
The comparative roles of dopaminergic and serotonergic mechanisms in mediating quipazine induced increases in locomotor activity.多巴胺能和5-羟色胺能机制在介导喹哌嗪引起的运动活性增加中的比较作用。
J Neural Transm. 1983;57(1-2):27-37. doi: 10.1007/BF01250045.
5
Role of 5HT in the morbidity of cerebral infarction-a study in the gerbil stroke model.5-羟色胺在脑梗死发病中的作用——沙鼠脑卒中模型研究
J Neurol Neurosurg Psychiatry. 1981 Feb;44(2):140-3. doi: 10.1136/jnnp.44.2.140.
6
Role of serotonin in memory: facilitation by alaproclate and zimeldine.血清素在记忆中的作用:阿普氯胺和齐美利定的促进作用。
Psychopharmacology (Berl). 1984;84(4):496-502. doi: 10.1007/BF00431456.
7
A behavioural and biochemical study in rats of 5-hydroxytryptamine receptor agonists and antagonists, with observations on structure-activity requirements for the agonists.一项关于5-羟色胺受体激动剂和拮抗剂在大鼠身上的行为与生化研究,并对激动剂的构效关系要求进行了观察。
Br J Pharmacol. 1981 Jul;73(3):703-19. doi: 10.1111/j.1476-5381.1981.tb16806.x.
8
beta-Adrenoceptor agonists enhance 5-hydroxytryptamine-mediated behavioural responses.β-肾上腺素能受体激动剂增强5-羟色胺介导的行为反应。
Br J Pharmacol. 1982 Jun;76(2):265-70. doi: 10.1111/j.1476-5381.1982.tb09216.x.
9
Efflux of 3H-5-hydroxytryptamine from rat hypothalamic slices by continuous electrical stimulation: frequency-dependent responses to serotonergic antagonists and 5-hydroxytryptamine.通过连续电刺激使3H-5-羟色胺从大鼠下丘脑切片中流出:对血清素能拮抗剂和5-羟色胺的频率依赖性反应。
Naunyn Schmiedebergs Arch Pharmacol. 1985 Jun;329(4):359-66. doi: 10.1007/BF00496368.
10
Evidence for selective serotonergic receptor involvement in p-chloroamphetamine-induced antinociception.选择性5-羟色胺能受体参与对氯苯丙胺诱导的抗伤害感受的证据。
Naunyn Schmiedebergs Arch Pharmacol. 1985 Apr;329(2):135-40. doi: 10.1007/BF00501202.