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Neuroleptic drugs block both the hyperactivity and the increase in caudate nucleus cyclic AMP concentration produced by the administration of tranylcypromine and L-dopa to rats.

作者信息

Heal D J, Green A R, Bloomfield M R, Grahame-Smith D G

出版信息

Psychopharmacology (Berl). 1978 Apr 28;57(2):193-7. doi: 10.1007/BF00426887.

DOI:10.1007/BF00426887
PMID:26101
Abstract

Injection of rats with tranylcypromine and L-dopa increased brain dopamine concentrations and produced a behavioural syndrome that includes hyperactivity. It also elevated caudate nucleus cyclic AMP concentrations by approximately 50% in vivo, probably by stimulating dopamine receptors. Pretreatment with chlorpromazine inhibited both the tranylcypromine/L-dopa-induced behaviour and elevated cyclic AMP concentrations in a dose-dependent manner. Haloperidol and alpha-flupenthixol also inhibited both effects, while beta-flupenthixol and pimozide were without effect. Since none of these drugs altered the tranylcypromine/L-dopa-induced rise of brain dopamine, it is likely that they produced their effect by inhibiting dopamine-sensitive adenylate cyclase. A good correlation was found to exist between the neuroleptic inhibition of both the increased behavioural activity and the increased caudate nucleus cyclic AMP concentrations produced by tranylcypromine and L-dopa.

摘要

相似文献

1
Neuroleptic drugs block both the hyperactivity and the increase in caudate nucleus cyclic AMP concentration produced by the administration of tranylcypromine and L-dopa to rats.
Psychopharmacology (Berl). 1978 Apr 28;57(2):193-7. doi: 10.1007/BF00426887.
2
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Cyclic adenosine monophosphate: selective increase in caudate nucleus after administration of L-dopa.
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Repeated chlorpromazine administration increases a behavioural response of rats to 5-hydroxytryptamine receptor stimulation.重复给予氯丙嗪会增强大鼠对5-羟色胺受体刺激的行为反应。
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Neuropharmacology. 1984 May;23(5):545-53. doi: 10.1016/0028-3908(84)90028-5.

引用本文的文献

1
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.

本文引用的文献

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A SENSITIVE METHOD FOR SPECTROPHOTOFLUOROMETRIC ASSAY OF CATECHOLAMINES.一种用于儿茶酚胺分光光度荧光测定的灵敏方法。
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Antagonism of apomorphine-induced sterotypy and emesis in dogs by thioridazine, haloperidol, and pimozide.硫利达嗪、氟哌啶醇和匹莫齐特对阿扑吗啡诱导的犬刻板行为和呕吐的拮抗作用。
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Antipsychotic drugs and dopamine-stimulated adenylate cyclase prepared from corpus striatum of rat brain.
抗精神病药物与从大鼠脑纹状体制备的多巴胺刺激的腺苷酸环化酶。
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The role of brain dopamine in the hyperactivity syndrome produced by increased 5-hydroxytryptamine synthesis in rats.脑多巴胺在大鼠5-羟色胺合成增加所产生的多动综合征中的作用。
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Dopamine-sensitive adenylate cyclase in caudate nucleus of rat brain, and its similarity to the "dopamine receptor".大鼠脑尾状核中对多巴胺敏感的腺苷酸环化酶及其与“多巴胺受体”的相似性。
Proc Natl Acad Sci U S A. 1972 Aug;69(8):2145-9. doi: 10.1073/pnas.69.8.2145.
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Adenosine 3',5'-monophosphate content in rat caudate nucleus: demonstration of dopaminergic and adrenergic receptors.大鼠尾状核中3',5'-环磷酸腺苷含量:多巴胺能和肾上腺素能受体的证明
Science. 1974 Dec 20;186(4169):1118-20. doi: 10.1126/science.186.4169.1118.
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Cyclic adenosine monophosphate: selective increase in caudate nucleus after administration of L-dopa.
Science. 1974 Feb 8;183(4124):532-3. doi: 10.1126/science.183.4124.532.
8
A protein binding assay for adenosine 3':5'-cyclic monophosphate.一种用于检测3':5'-环磷酸腺苷的蛋白质结合测定法。
Proc Natl Acad Sci U S A. 1970 Sep;67(1):305-12. doi: 10.1073/pnas.67.1.305.
9
Studies in vivo on the relationship between brain tryptophan, brain 5-HT synthesis and hyperactivity in rats treated with a monoamine oxidase inhibitor and L-tryptophan.关于用单胺氧化酶抑制剂和L-色氨酸处理的大鼠中脑色氨酸、脑5-羟色胺合成与多动之间关系的体内研究。
J Neurochem. 1971 Jun;18(6):1053-66. doi: 10.1111/j.1471-4159.1971.tb12034.x.
10
Dopamine-sensitive adenylate cyclase in mammalian brain: a possible site of action of antipsychotic drugs.哺乳动物脑中对多巴胺敏感的腺苷酸环化酶:抗精神病药物的一个可能作用位点。
Proc Natl Acad Sci U S A. 1974 Apr;71(4):1113-7. doi: 10.1073/pnas.71.4.1113.