氟哌啶醇的药理学与生物化学 - Suppr

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超能文献

Pharmacology and biochemistry of haloperidol.

作者信息

Niemegeers C J, Laduron P M

出版信息

Proc R Soc Med. 1976;69 suppl 1(Suppl 1):3-8. doi: 10.1177/00359157760690S102.

DOI:10.1177/00359157760690S102

PMID:14331

原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1863606/

Abstract

摘要

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a79a/1863606/848561df4158/procrsmed00036-0008-a.jpg

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Pharmacology and biochemistry of haloperidol.氟哌啶醇的药理学与生物化学

Proc R Soc Med. 1976;69 suppl 1(Suppl 1):3-8. doi: 10.1177/00359157760690S102.

Pharmacology and biochemistry of bromperidol.溴哌利多的药理学与生物化学

Acta Psychiatr Belg. 1978 Jan-Feb;78(1):37-50.

Pimozide, a chemically novel, highly potent and orally long-acting neuroleptic drug. I. The comparative pharmacology of pimozide, haloperidol, and chlorpromazine.匹莫齐特，一种化学结构新颖、高效且口服长效的抗精神病药物。I. 匹莫齐特、氟哌啶醇和氯丙嗪的比较药理学。

Arzneimittelforschung. 1968 Mar;18(3):261-79.

No evidence for increased dopamine receptor binding in superresponsive mice after a single dose of neuroleptics.单次给予抗精神病药物后，超反应小鼠中多巴胺受体结合增加无证据支持。

Adv Biochem Psychopharmacol. 1980;24:167-73.

[Problem of neuronal reception and the dopamine hypothesis of schizophrenia].[神经元接收问题与精神分裂症的多巴胺假说]

Zh Nevropatol Psikhiatr Im S S Korsakova. 1980;80(5):762-9.

Pharmacological properties of a new potential neuroleptic drug oxyprothepin. IV. Antiadrenergic action and influence on brain monoamines.一种新型潜在抗精神病药物奥昔普明的药理特性。IV. 抗肾上腺素能作用及对脑单胺的影响。

Act Nerv Super (Praha). 1971;13(3):188-9.

[Effect of neuroleptic agents in the chronic pharmacological experiment].[抗精神病药物在慢性药理学实验中的作用]

Arzneimittelforschung. 1974 Sep;24(9):1292-4.

[Metabolism of dopamine and norepinephrine in rat brain after acute and chronic administration of haloperidol, loxapine and clozapine].[急性和慢性给予氟哌啶醇、洛沙平及氯氮平后大鼠脑内多巴胺和去甲肾上腺素的代谢]

Arzneimittelforschung. 1974 Jul;24(7):983-4.

Bromoperidol, a new potent neuroleptic of the butyrophenone series. Comparative pharmacology of bromoperidol and haloperidol.溴哌利多，一种新型强效丁酰苯类神经安定药。溴哌利多与氟哌啶醇的比较药理学。

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Dopamine-stimulated adenylate cyclase in rat substantia nigra: localization and effects of neuroleptics.大鼠黑质中多巴胺刺激的腺苷酸环化酶：定位及抗精神病药物的作用

Adv Biochem Psychopharmacol. 1977;16:613-6.

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Randomized Phase II Trial to Compare the Efficacy of Haloperidol and Olanzapine in the Control of Chemotherapy-Induced Nausea and Vomiting in Nepal.尼泊尔比较氟哌啶醇与奥氮平控制化疗引起的恶心和呕吐疗效的随机II期试验。

J Glob Oncol. 2019 Apr;5:1-6. doi: 10.1200/JGO.18.00245.

T-derived dopamine accelerates productive synapses in germinal centres.T衍生的多巴胺可加速生发中心的有效突触形成。

Nature. 2017 Jul 20;547(7663):318-323. doi: 10.1038/nature23013. Epub 2017 Jul 12.

Open-label study comparing the efficacy and tolerability of aripiprazole and haloperidol in the treatment of pediatric tic disorders.一项开放性研究比较阿立哌唑和氟哌啶醇治疗儿科抽动障碍的疗效和耐受性。

Eur Child Adolesc Psychiatry. 2011 Mar;20(3):127-35. doi: 10.1007/s00787-010-0154-0. Epub 2010 Dec 28.

Fentanyl, but not haloperidol, entrains persisting circadian activity episodes when administered at 24- and 31-h intervals.芬太尼，而不是氟哌啶醇，在 24 小时和 31 小时的间隔时间给药时会引发持续的昼夜节律活动发作。

Behav Brain Res. 2009 Dec 14;205(1):102-14. doi: 10.1016/j.bbr.2009.07.002. Epub 2009 Jul 10.

Specific effect of haloperidol on dopamine turnover in the frontal cortex.氟哌啶醇对额叶皮质中多巴胺周转的特定作用。

Naunyn Schmiedebergs Arch Pharmacol. 1977 Jan;296(2):183-5. doi: 10.1007/BF00508472.

Chromopharmacological study of neuroleptics. III. Circadian rhythm of brain susceptibility to haloperidol.抗精神病药物的色药理学研究。III. 大脑对氟哌啶醇敏感性的昼夜节律。

Psychopharmacology (Berl). 1979 May 25;63(2):131-5. doi: 10.1007/BF00429690.

本文引用的文献

Chemistry and pharmacology of compounds related to 4-(4-hydroxy-4-phenyl-piperidino)-butvrophenone.与4-(4-羟基-4-苯基哌啶基)丁酰苯相关的化合物的化学与药理学

Arzneimittelforschung. 1959 Dec;9:765-7.

Chemistry and pharmacology of CNS depressants related to 4-(4-hydroxy-phenylpiperidino)butyrophenone. I. Synthesis and screening data in mice.与4-(4-羟基苯基哌啶基)丁酰苯相关的中枢神经系统抑制剂的化学与药理学。I. 小鼠体内的合成与筛选数据

J Med Pharm Chem. 1959 Jun;1:281-97. doi: 10.1021/jm50004a007.

EFFECT OF CHLORPROMAZINE OR HALOPERIDOL ON FORMATION OF 3METHOXYTYRAMINE AND NORMETANEPHRINE IN MOUSE BRAIN.氯丙嗪或氟哌啶醇对小鼠脑内3-甲氧基酪胺和去甲变肾上腺素形成的影响。

Acta Pharmacol Toxicol (Copenh). 1963;20:140-4. doi: 10.1111/j.1600-0773.1963.tb01730.x.

A comparative study of the effect of subcutaneous and oral doses of haloperidol on avoidance-escape habits of rats and dogs in a "jumping box" situation.皮下注射与口服氟哌啶醇对大鼠和犬在“跳箱”情境中回避-逃避习性影响的比较研究。

Arzneimittelforschung. 1963 May;13:401-3.

Chemistry and pharmacology of compounds related to 4-(4-hydroxy-4-phenyl-piperidino)-butyrophenone. III. Duration of antiemetic action and oral effectiveness of Haloperidol (R 1625) and of chlorpromazine in dogs.与4-(4-羟基-4-苯基-哌啶基)-丁酰苯相关化合物的化学与药理学。III. 氟哌啶醇（R 1625）和氯丙嗪在犬体内的止吐作用持续时间及口服效果

Arzneimittelforschung. 1960 Nov;10:955.

Apomorphine-antagonism in rats.大鼠中的阿扑吗啡拮抗作用。

Arzneimittelforschung. 1960 Dec;10:1003-5.

Influence of haloperidol (R 1625) and of haloperidide (R 3201) on avoidance and escape behavior of trained dogs in a "jumping box".氟哌啶醇（R 1625）和氟哌啶（R 3201）对经训练的犬在“跳箱”实验中回避和逃避行为的影响。

J Pharm Pharmacol. 1960 Dec;12:744-53. doi: 10.1111/j.2042-7158.1960.tb12741.x.

The significance of dopamine-receptor blockade for the mechanism of action of neuroleptic drugs.多巴胺受体阻断对抗精神病药物作用机制的意义。

Arch Int Pharmacodyn Ther. 1966 Apr;160(2):492-4.

Is it possible to predict the clinical effects of neuroleptic drugs (major tranquillizers) from animal data? IV. An improved experimental design for measuring the inhibitory effects of neuroleptic drugs on amphetamine-or apomorphine-induced "Cheroing" and "agitation" in rats.能否从动物实验数据预测抗精神病药物（强效镇静剂）的临床效果？IV. 一种改进的实验设计，用于测量抗精神病药物对大鼠中苯丙胺或阿扑吗啡诱导的“刻板行为”和“激动”的抑制作用。

Arzneimittelforschung. 1967 Jul;17(7):841-54.

Mode of action of apomorphine and dexamphetamine on gnawing compulsion in rats.阿扑吗啡和右旋苯丙胺对大鼠啃咬强迫行为的作用机制

Psychopharmacologia. 1967;10(4):316-23. doi: 10.1007/BF00403900.

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