标准抗精神病化合物对大鼠纹状体和中脑边缘系统中3H-螺哌啶醇体外结合的影响。 - Suppr

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超能文献

The effects of standard neuroleptic compounds on the binding of 3H-spiroperidol in the striatum and mesolimbic system of the rat in vitro.

作者信息

Howard J L, Large B T, Wedley S, Pullar I A

出版信息

Life Sci. 1978 Aug 14;23(6):599-603. doi: 10.1016/0024-3205(78)90039-5.

DOI:10.1016/0024-3205(78)90039-5

PMID:29198

Abstract

摘要

相似文献

The effects of standard neuroleptic compounds on the binding of 3H-spiroperidol in the striatum and mesolimbic system of the rat in vitro.标准抗精神病化合物对大鼠纹状体和中脑边缘系统中3H-螺哌啶醇体外结合的影响。

Life Sci. 1978 Aug 14;23(6):599-603. doi: 10.1016/0024-3205(78)90039-5.

Two binding sites for 3H-spiroperidol on rat striatal membranes.大鼠纹状体膜上3H-螺哌啶醇的两个结合位点。

Eur J Pharmacol. 1978 Aug 1;50(3):283-4. doi: 10.1016/0014-2999(78)90363-1.

3H-Spiroperidol binding to two receptor sites in both the corpus striatum and frontal cortex of rat brain.3H-螺哌利多与大鼠脑纹状体和额叶皮质中的两个受体位点结合。

Eur J Pharmacol. 1978 Aug 15;50(4):451-3. doi: 10.1016/0014-2999(78)90154-1.

Spiperone: a ligand of choice for neuroleptic receptors. 1. Kinetics and characteristics of in vitro binding.螺哌隆：一种用于抗精神病药物受体的理想配体。1. 体外结合的动力学和特性

Biochem Pharmacol. 1978 Feb 1;27(3):307-16. doi: 10.1016/0006-2952(78)90233-2.

Increased 3H-spiperone binding sites in mesolimbic area related to methamphetamine-induced behavioral hypersensitivity.中脑边缘区域中与甲基苯丙胺诱导的行为过敏相关的³H-螺哌隆结合位点增加。

Biol Psychiatry. 1982 Feb;17(2):223-31.

Effect of timiperone on 3H-spiroperidol binding to rat striatal dopamine receptors.替米哌隆对3H-螺哌啶醇与大鼠纹状体多巴胺受体结合的影响。

Eur J Pharmacol. 1979 Nov 16;59(3-4):245-51. doi: 10.1016/0014-2999(79)90287-5.

A comparative study of [3H]haloperidol and [3H]spiroperidol binding to receptors on rat cerebral membranes.[3H]氟哌啶醇与[3H]螺哌啶醇结合大鼠脑膜受体的比较研究。

FEBS Lett. 1978 Mar 1;87(1):152-6. doi: 10.1016/0014-5793(78)80155-0.

Ex vivo 3H-spiroperidol binding to rat striatum and the inhibitory effects of neuroleptics.离体3H-螺哌啶醇与大鼠纹状体的结合及抗精神病药物的抑制作用。

Jpn J Pharmacol. 1981 Apr;31(2):159-64. doi: 10.1254/jjp.31.159.

Comparison of the effects of substituted benzamides and standard neuroleptics on the binding of 3H-spiroperidol in the rat pituitary and striatum with in vivo effects on rat prolactin secretion.取代苯甲酰胺类药物与标准抗精神病药物对大鼠垂体和纹状体中3H-螺哌啶结合的影响及其对大鼠催乳素分泌的体内效应比较。

Life Sci. 1979 Aug 13;25(7):573-83. doi: 10.1016/0024-3205(79)90551-4.

Anomalous properties of [3H]spiperone binding sites in various areas of the rat limbic system.大鼠边缘系统各区域中[3H]司哌罗宁结合位点的异常特性。

Mol Pharmacol. 1979 May;15(3):506-14.

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Atypical neuroleptics increase self-administration of cocaine: an evaluation of a behavioural screen for antipsychotic activity.非典型抗精神病药物会增加可卡因的自我给药：一项抗精神病活性行为筛选评估

Psychopharmacology (Berl). 1984;82(1-2):135-9. doi: 10.1007/BF00426397.

Metoclopramide: antipsychotic efficacy of a drug lacking potency in receptor models.甲氧氯普胺：一种在受体模型中缺乏效力的药物的抗精神病疗效。

Psychopharmacology (Berl). 1980;71(3):219-25. doi: 10.1007/BF00433055.

Blockade of acquisition of one-way conditioned avoidance responding by haloperidol and metoclopramide but not by thioridazine or clozapine: implications for screening new antipsychotic drugs.氟哌啶醇和胃复安可阻断单向条件性回避反应的习得，但硫利达嗪或氯氮平则不然：这对筛选新型抗精神病药物具有启示意义。

Psychopharmacology (Berl). 1989;98(4):453-9. doi: 10.1007/BF00441941.

In vitro and in vivo disposition of 3H-methiothepin in brain tissues. Relationship to the effects of acute treatment with methiothepin on central serotoninergic receptors.3H-甲硫噻吨在脑组织中的体外和体内处置。与甲硫噻吨急性治疗对中枢5-羟色胺能受体的影响的关系。

Naunyn Schmiedebergs Arch Pharmacol. 1979 Dec;310(1):25-33. doi: 10.1007/BF00499871.

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