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匹莫齐特:其药理学特性及在精神病学中的治疗用途综述

Pimozide: a review of its pharmacological properties and therapeutic uses in psychiatry.

作者信息

Pinder R M, Brogden R N, Swayer R, Speight T M, Spencer R, Avery G S

出版信息

Drugs. 1976;12(1):1-40. doi: 10.2165/00003495-197612010-00001.

DOI:10.2165/00003495-197612010-00001
PMID:824116
Abstract

Pimozide 1-(1-[4,4-bis(4-fluorophenyl)butyl]-4-peperidinyl)-2-benzimidazolone, is the first of a new series of psychotropic drugs, the kiphenylbutylpiperidines. It is advocated for once-daily use as maintenance therapy in chronic schizophrenia and for the treatment of psychic and functional disorders induced by personality traits. Published data suggest that in chronic schizophrenia, pimozide 4 to 6mg daily is indistinguishable from maintenance doses of chlorpromazine, fluphenazine, flupenthixol, perphenazine, or thioidazine. Patient groups have usually been to small to allow statistically significant differences to be apparent, but in some trials pimozide was significantly superior to trifluoperzine and to haloperidol. On present evidence, pimozide has no place in the hyperactive, aggressive type of patient or in treating the acute phase of schizophrenia, probably because of its relative lack of sedative properties compared with many antipsychotic drugs. The incidence and severity of extrapyramidal reactions with pimozide are low, but suitably designed controlled studies are needed to determine whether its use leads to a reduction in the requirement for antiparkinsonian medication. In anxious patients, pimozide seems to offer no advantages over currently available anxiolytic agents, either in terms of efficacy or incidence of side-effects. Claims for a specific effect against anxiety associated with psychosis or disturbed personality traits remain unproven.

摘要

匹莫齐特1-(1-[4,4-双(4-氟苯基)丁基]-4-哌啶基)-2-苯并咪唑酮,是一类新型精神药物——联苯基丁基哌啶类中的首个药物。它被推荐用于慢性精神分裂症的每日一次维持治疗以及治疗由人格特质引起的精神和功能障碍。已发表的数据表明,在慢性精神分裂症中,每日4至6毫克的匹莫齐特与氯丙嗪、氟奋乃静、氟哌噻吨、奋乃静或硫利达嗪的维持剂量效果相当。患者群体通常规模较小,难以显现出具有统计学意义的差异,但在一些试验中,匹莫齐特显著优于三氟拉嗪和氟哌啶醇。根据目前的证据,匹莫齐特在治疗多动、攻击性类型的患者或精神分裂症急性期方面并无用武之地,这可能是因为与许多抗精神病药物相比,它相对缺乏镇静作用。匹莫齐特引起锥体外系反应的发生率和严重程度较低,但需要进行设计合理的对照研究,以确定其使用是否会减少抗帕金森药物的需求。在焦虑患者中,无论是在疗效还是副作用发生率方面,匹莫齐特似乎都不比现有的抗焦虑药物更具优势。关于其对与精神病或人格特质紊乱相关的焦虑有特效的说法尚未得到证实。

相似文献

1
Pimozide: a review of its pharmacological properties and therapeutic uses in psychiatry.匹莫齐特:其药理学特性及在精神病学中的治疗用途综述
Drugs. 1976;12(1):1-40. doi: 10.2165/00003495-197612010-00001.
2
Pimozide versus Haloperidol in acute schizophrenia. A double blind controlled study.匹莫齐特与氟哌啶醇治疗急性精神分裂症的双盲对照研究。
Pharmacopsychiatria. 1982 Mar;15(2):70-4. doi: 10.1055/s-2007-1019512.
3
Tardive dyskinesia treated with pimozide.用匹莫齐特治疗迟发性运动障碍。
J Neurol Sci. 1975 Apr;24(4):393-401. doi: 10.1016/0022-510x(75)90165-3.
4
Clinical uses of pimozide.匹莫齐特的临床应用。
South Med J. 1993 Mar;86(3):344-9. doi: 10.1097/00007611-199303000-00019.
5
Clinical trial of pimozide.
West Afr J Pharmacol Drug Res. 1976 Jun;3(1):17-24.
6
Pimozide versus fluphenazine in ambulatory schizophrenics: A 12-month comparison study.匹莫齐特与氟奋乃静治疗门诊精神分裂症患者的12个月对比研究。
Dis Nerv Syst. 1977 Feb;38(2):119-23.
7
Pimozide as an adjuvant to maintenance therapy in chronic schizophrenia.匹莫齐特作为慢性精神分裂症维持治疗的辅助药物。
Pharmatherapeutica. 1980;2(5):337-40.
8
A series of multicentric pilot trials with pimozide in psychiatric practice. 3. Pimozide in the treatment of stress-induced psychic and functional disorders.在精神科实践中使用匹莫齐特的一系列多中心试点试验。3. 匹莫齐特治疗应激所致精神和功能障碍
Acta Psychiatr Belg. 1972 Nov;72(6):671-6.
9
Pimozide: use in dermatology.匹莫齐特:在皮肤科的应用。
Dermatol Online J. 2003 Mar;9(2):3.
10
[Dose-effect relations. Doubleblind study on two different doses of pimozide (author's transl)].剂量效应关系。两种不同剂量匹莫齐特的双盲研究(作者译)
Arzneimittelforschung. 1978;28(9):1491-2.

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THE NURSES' OBSERVATION SCALE FOR INPATIENT EVALUATION: A NEW SCALE FOR MEASURING IMPROVEMENT IN CHRONIC SCHIZOPHRENIA.住院患者评估护士观察量表:一种用于测量慢性精神分裂症改善情况的新量表。
J Clin Psychol. 1965 Jan;21:65-71. doi: 10.1002/1097-4679(196501)21:1<65::aid-jclp2270210122>3.0.co;2-i.
2
The metabolism and excretion of the neuroleptic drug pimozide (R 6238) by the wistar rat.抗精神病药物匹莫齐特(R 6238)在Wistar大鼠体内的代谢与排泄
Life Sci. 1969 Mar 1;8(5):291-5. doi: 10.1016/0024-3205(69)90279-3.
3
Pimozide, a chemically novel, highly potent and orally long-acting neuroleptic drug. 3. Regional distribution of pimozide and of haloperidol in the dog brain.
匹莫齐特与己二酸:一种改善药物性能的新型多组分晶体实体。
Molecules. 2024 Nov 27;29(23):5610. doi: 10.3390/molecules29235610.
4
MGACL: Prediction Drug-Protein Interaction Based on Meta-Graph Association-Aware Contrastive Learning.MGACL:基于元图关联感知对比学习的药物-蛋白质相互作用预测。
Biomolecules. 2024 Oct 8;14(10):1267. doi: 10.3390/biom14101267.
5
Ferrocenium Boronic Acid Catalyzed Deoxygenative Coupling of Alcohols with Carbon- and Nitrogen-Based Borate and Silane Nucleophiles.二茂铁硼酸催化的醇与碳、氮硼酸和硅烷亲核试剂的脱氧偶联反应。
J Org Chem. 2023 Jul 7;88(13):8505-8511. doi: 10.1021/acs.joc.3c00463. Epub 2023 Jun 7.
6
Antipsychotic drug-aripiprazole against schizophrenia, its therapeutic and metabolic effects associated with gene polymorphisms.抗精神分裂症药物-阿立哌唑,其治疗和代谢作用与基因多态性相关。
Pharmacol Rep. 2023 Feb;75(1):19-31. doi: 10.1007/s43440-022-00440-6. Epub 2022 Dec 16.
7
The Respective Roles of CYP3A4 and CYP2D6 in the Metabolism of Pimozide to Established and Novel Metabolites.CYP3A4 和 CYP2D6 在匹莫齐特代谢为现有和新代谢物中的各自作用。
Drug Metab Dispos. 2020 Nov;48(11):1113-1120. doi: 10.1124/dmd.120.000188. Epub 2020 Aug 26.
8
Loperamide, pimozide, and STF-62247 trigger autophagy-dependent cell death in glioblastoma cells.洛哌丁胺、匹莫齐特和 STF-62247 可诱导神经胶质瘤细胞发生自噬依赖性细胞死亡。
Cell Death Dis. 2018 Sep 24;9(10):994. doi: 10.1038/s41419-018-1003-1.
9
Neuroleptics as therapeutic compounds stabilizing neuromuscular transmission in amyotrophic lateral sclerosis.神经安定剂作为治疗化合物,稳定肌萎缩性侧索硬化症中的神经肌肉传递。
JCI Insight. 2017 Nov 16;2(22). doi: 10.1172/jci.insight.97152.
10
A Screen of FDA-Approved Drugs for Inhibitors of Zika Virus Infection.对美国食品药品监督管理局(FDA)批准的用于寨卡病毒感染抑制剂的药物进行筛选。
Cell Host Microbe. 2016 Aug 10;20(2):259-70. doi: 10.1016/j.chom.2016.07.004. Epub 2016 Jul 28.
Arzneimittelforschung. 1968 Mar;18(3):282-7.
4
Pimozide, a chemically novel, highly potent and orally long-acting neuroleptic drug. II. Kinetic study of the distribution of pimozide and metabolites in brain, liver, and blood of the Wistar rat.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。II. 匹莫齐特及其代谢产物在Wistar大鼠脑、肝和血液中分布的动力学研究。
Arzneimittelforschung. 1968 Mar;18(3):279-82.
5
Pupillary paralysis after tranquilizer.镇静剂使用后瞳孔麻痹。
Br Med J. 1971 Sep 11;3(5775):639. doi: 10.1136/bmj.3.5775.639-b.
6
Pupillary paralysis after tranquillizer.安定剂使用后出现瞳孔麻痹。
Br Med J. 1971 Aug 26;3(5773):530-1. doi: 10.1136/bmj.3.5773.530-c.
7
Receptor activity and turnover of dopamine and noradrenaline after neuroleptics.抗精神病药物治疗后多巴胺和去甲肾上腺素的受体活性及更新率
Eur J Pharmacol. 1970;11(3):303-14. doi: 10.1016/0014-2999(70)90006-3.
8
[Therapy of schizophrenic syndromes with a delayed-action drug: pimozide].[使用长效药物匹莫齐特治疗精神分裂症综合征]
Clin Ter. 1971 Jul;57(6):527-39.
9
[A new antipsychotic drug: pimozide R 6238. Clinical evaluation].[一种新型抗精神病药物:匹莫齐特R 6238。临床评估]
Prensa Med Argent. 1971 Sep;58(28):1444-9.
10
Pimozide: EEG effects related to clinical response.匹莫齐特:与临床反应相关的脑电图效应。
Can Psychiatr Assoc J. 1971 Oct;16(5):437-9. doi: 10.1177/070674377101600509.