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Presynaptic dopamine receptors. Development of supersensitivity following treatment with fluphenazine decanoate.

作者信息

Nowycky M C, Roth R H

出版信息

Naunyn Schmiedebergs Arch Pharmacol. 1977 Nov;300(3):247-54.

PMID:600312
Abstract
摘要

相似文献

1
Presynaptic dopamine receptors. Development of supersensitivity following treatment with fluphenazine decanoate.突触前多巴胺受体。癸酸氟奋乃静治疗后超敏反应的发展。
Naunyn Schmiedebergs Arch Pharmacol. 1977 Nov;300(3):247-54.
2
Tolerance to fluphenazine and supersensitivity to apomorphine in central dopaminergic systems after chronic fluphenazine decanoate treatment.癸酸氟奋乃静长期治疗后中枢多巴胺能系统对氟奋乃静的耐受性及对阿扑吗啡的超敏反应。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Jun;312(2):151-9. doi: 10.1007/BF00569724.
3
Alterations in peripheral and central dopamine receptor sensitivity after subchronic treatment with fluphenazine and sulpiride.氟奋乃静和舒必利亚慢性治疗后外周和中枢多巴胺受体敏感性的改变。
Pharmacol Toxicol. 1987 Jul;61(1):48-52. doi: 10.1111/j.1600-0773.1987.tb01771.x.
4
Development of supersensitivity of apomorphine-induced increases in acetylcholine levels and stereotype after chronic fluphenazine treatment.慢性氟奋乃静治疗后阿扑吗啡诱导的乙酰胆碱水平升高和刻板行为超敏反应的发展。
Neuropharmacology. 1978 Jan;17(1):59-64. doi: 10.1016/0028-3908(78)90174-0.
5
Lack of a strong influence of neuroleptic decanoates on dopaminergic and GABAergic functions.长效抗精神病癸酸盐对多巴胺能和γ-氨基丁酸能功能缺乏强烈影响。
Pol J Pharmacol. 1995 Mar-Apr;47(2):99-107.
6
Antagonism of presynaptic dopamine receptors by phenothiazine drug metabolites.
Life Sci. 1990;46(6):443-51. doi: 10.1016/0024-3205(90)90088-9.
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Dopaminergic supersensitivity in striatum and olfactory tubercle following chronic administration of haloperidol or clozapine.
Life Sci. 1977 May 1;20(9):1585-91. doi: 10.1016/0024-3205(77)90452-0.
8
Yawning elicited by systemic and intrastriatal injection of piribedil and apomorphine in the rat.全身性及纹状体内注射匹立哌唑和阿扑吗啡诱发大鼠打哈欠。
Psychopharmacology (Berl). 1985;86(1-2):175-81. doi: 10.1007/BF00431705.
9
Inhibition of dopamine synthesis in rat striatal minces: evidence of dopamine autoreceptor supersensitivity to S(+)- but not R(-)-N-n-propylnorapomorphine after pretreatment with fluphenazine.氟奋乃静预处理后大鼠纹状体匀浆中多巴胺合成的抑制：多巴胺自身受体对S(+)-而非R(-)-N-正丙基去甲阿扑吗啡超敏反应的证据。
Biochem Pharmacol. 1991 Jun 15;41(12):2040-3. doi: 10.1016/0006-2952(91)90148-x.
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The effect of bradykinin on central dopamine receptors.缓激肽对中枢多巴胺受体的作用。
Pol J Pharmacol Pharm. 1976 Nov-Dec;28(6):673-8.

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Effects of antipsychotic treatment on psychopathology and motor symptoms. A placebo-controlled study in healthy volunteers.抗精神病药物治疗对精神病理学和运动症状的影响。一项在健康志愿者中进行的安慰剂对照研究。
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Supersensitivity of dopamine-autoreceptors. The effect of gammabutyrolactone in long-term haloperidol treated rats.

本文引用的文献

1
Enhancement of methylphenidate-induced stereotypies by repeated administration of neuroleptis.反复给予抗精神病药物增强哌醋甲酯引起的刻板行为
Psychopharmacologia. 1974 Jan 11;34(2):105-9. doi: 10.1007/BF00421934.
2
Dopaminergic neurons: effect of antipsychotic drugs and amphetamine on single cell activity.多巴胺能神经元：抗精神病药物和苯丙胺对单细胞活性的影响。
J Pharmacol Exp Ther. 1973 Jun;185(3):560-71.
3
Regulation of monoamine metabolism in the central nervous system.中枢神经系统中单胺代谢的调节。
多巴胺自身受体的超敏反应。γ-丁内酯对长期服用氟哌啶醇大鼠的影响。
J Neural Transm. 1980;47(2):145-51. doi: 10.1007/BF01670165.
4
Tolerance to fluphenazine and supersensitivity to apomorphine in central dopaminergic systems after chronic fluphenazine decanoate treatment.癸酸氟奋乃静长期治疗后中枢多巴胺能系统对氟奋乃静的耐受性及对阿扑吗啡的超敏反应。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Jun;312(2):151-9. doi: 10.1007/BF00569724.
5
The Yawning elicited by alpha-melanocyte-stimulating hormone involves serotonergic-dopaminergic-cholinergic neuron link in rats.α-黑素细胞刺激素引发的打哈欠涉及大鼠体内的5-羟色胺能-多巴胺能-胆碱能神经元联系。
Naunyn Schmiedebergs Arch Pharmacol. 1981 Apr;316(2):155-60. doi: 10.1007/BF00505310.
6
Enhancement of haloperidol-induced increase in rat striatal or mesolimbic 3,4-dihydroxyphenylacetic acid and homovanillic acid by pretreatment with chronic methamphetamine.慢性甲基苯丙胺预处理增强氟哌啶醇诱导的大鼠纹状体或中脑边缘系统3,4-二羟基苯乙酸和高香草酸的增加。
Psychopharmacology (Berl). 1981;74(4):316-20. doi: 10.1007/BF00432738.
7
Presynaptic dopamine receptors: insensitivity to kainic acid and the development of supersensitivity following chronic haloperidol.突触前多巴胺受体：对 kainic 酸不敏感及慢性氟哌啶醇后超敏反应的发展。
Naunyn Schmiedebergs Arch Pharmacol. 1980 Jun;312(2):161-5. doi: 10.1007/BF00569725.
8
Direct evidence for involvement of dopaminergic inhibition and cholinergic activation in yawning.多巴胺能抑制和胆碱能激活参与打哈欠的直接证据。
Psychopharmacology (Berl). 1980 Jan;67(1):39-43. doi: 10.1007/BF00427593.
9
A comparison of the potencies of various dopamine receptor agonists in models for pre- and postsynaptic receptor activity.
Naunyn Schmiedebergs Arch Pharmacol. 1983 Sep;324(2):108-15. doi: 10.1007/BF00497015.
10
Response changes after repeated low apomorphine: dopamine autoreceptor desensitization or learning?重复给予低剂量阿扑吗啡后的反应变化：多巴胺自身受体脱敏还是学习效应？
Psychopharmacology (Berl). 1984;83(2):188-93. doi: 10.1007/BF00429733.
Pharmacol Rev. 1972 Jun;24(2):371-84.
4
A model for the quantitative study of central dopaminergic and serotoninergic activity.一种用于中枢多巴胺能和5-羟色胺能活性定量研究的模型。
Eur J Pharmacol. 1972 Apr;18(1):128-36. doi: 10.1016/0014-2999(72)90140-9.
5
Pharmacologically induced behavioural supersensitivity to apomorphine.药物诱导的对阿扑吗啡的行为超敏反应。
Nat New Biol. 1973 Oct 31;245(148):262-3. doi: 10.1038/newbio245262a0.
6
Comparison of effects of L-dopa, amphetamine and apomorphine on firing rate of rat dopaminergic neurones.左旋多巴、苯丙胺和阿扑吗啡对大鼠多巴胺能神经元放电频率影响的比较。
Nat New Biol. 1973 Sep 26;245(143):123-5. doi: 10.1038/newbio245123a0.
7
Evidence for a new type of dopamine receptor stimulating agent.新型多巴胺受体激动剂的证据。
J Pharm Pharmacol. 1971 Dec;23(12):989-91. doi: 10.1111/j.2042-7158.1971.tb09916.x.
8
Striatal dopamine release after amphetamine or nerve degeneration revealed by rotational behaviour.通过旋转行为揭示的苯丙胺或神经变性后的纹状体多巴胺释放。
Acta Physiol Scand Suppl. 1971;367:49-68. doi: 10.1111/j.1365-201x.1971.tb10999.x.
9
The pharmacology of tardive dyskinesias.迟发性运动障碍的药理学
Am J Psychiatry. 1973 Jan;130(1):82-6. doi: 10.1176/ajp.130.1.82.
10
A method for the determination of 3,4-dihydroxyphenylalanine (DOPA) in brain.一种测定脑中3,4-二羟基苯丙氨酸（多巴）的方法。
Naunyn Schmiedebergs Arch Pharmacol. 1972;274(3):273-80. doi: 10.1007/BF00501936.