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抗焦虑药物的行为学研究。V. 对增加受罚反应的药物在鸽子身上进行的行为学和体内神经化学分析。

Behavioral studies with anxiolytic drugs. V. Behavioral and in vivo neurochemical analyses in pigeons of drugs that increase punished responding.

作者信息

Mansbach R S, Harrod C, Hoffmann S M, Nader M A, Lei Z, Witkin J M, Barrett J E

机构信息

Department of Psychiatry, Uniformed Services University of the Health Sciences, Bethesda, Maryland.

出版信息

J Pharmacol Exp Ther. 1988 Jul;246(1):114-20.

PMID:2455786
Abstract

Behavioral and neurochemical effects of several drugs that increase punished responding were studied in pigeons. Key pecking was established under a schedule of reinforcement in which periods of food-maintained responding alternated with periods in which behavior also was suppressed by the presentation of electric shock. Buspirone (0.1-10.0 mg/kg), gepirone (0.1-1.0 mg/kg), 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT; 0.1-3.0 mg/kg), chlordiazepoxide (3.0-30.0 mg/kg) and to a lesser extent clozapine (0.1-1.0 mg/kg) all produced increases in punished responding at doses having little effect on or decreasing the rate of unpunished responding. Neurochemical analyses on samples of cerebrospinal fluid after administration of several doses of each compound were performed for the dopamine metabolites homovanillic acid (HVA) and dihydroxyphenylacetic acid (DOPAC), the noradrenergic metabolite 3-methoxy-4-hydroxyphenylethylene glycol (MHPG) and the serotonin metabolite 5-hydroxyindoleacetic acid (5-HIAA). Gepirone, 8-OH-DPAT and the novel anxiolytic buspirone produced decreases in 5-HIAA at doses that increased punished responding in the behavioral studies. Buspirone increased levels of HVA and DOPAC, whereas its structural analog gepirone and the 5-hydroxytryptamine1A agonist 8-OH-DPAT had little effect on or decreased levels of these metabolites. Chlordiazepoxide, a prototypic benzodiazepine anxiolytic, produced only modest decreases in each of the metabolites studied. Clozapine, an atypical antipsychotic drug, produced increases in each of the metabolites studied, although only the 5-HIAA effect occurred at doses that were not behaviorally disruptive. Haloperidol (0.03-1.0 mg/kg) produced only decreases in punished and unpunished responding, whereas eliciting increases in the appearance of MHPG, DOPAC and HVA; levels of 5-HIAA were relatively unaffected.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

研究了几种能增加受罚反应的药物对鸽子行为和神经化学的影响。在一种强化程序下建立按键啄击行为,即食物维持反应期与电击抑制行为期交替出现。丁螺环酮(0.1 - 10.0毫克/千克)、吉哌隆(0.1 - 1.0毫克/千克)、8 - 羟基 - 2 -(二正丙基氨基)四氢萘(8 - OH - DPAT;0.1 - 3.0毫克/千克)、氯氮卓(3.0 - 30.0毫克/千克)以及程度较轻的氯氮平(0.1 - 1.0毫克/千克),在对未受罚反应速率影响很小或降低未受罚反应速率的剂量下,均能增加受罚反应。对每种化合物给予几个剂量后采集的脑脊液样本进行神经化学分析,检测多巴胺代谢产物高香草酸(HVA)和二羟基苯乙酸(DOPAC)、去甲肾上腺素能代谢产物3 - 甲氧基 - 4 - 羟基苯乙二醇(MHPG)以及5 - 羟色胺代谢产物5 - 羟吲哚乙酸(5 - HIAA)。在行为学研究中,能增加受罚反应的剂量下,吉哌隆、8 - OH - DPAT和新型抗焦虑药丁螺环酮使5 - HIAA水平降低。丁螺环酮使HVA和DOPAC水平升高,而其结构类似物吉哌隆和5 - 羟色胺1A激动剂8 - OH - DPAT对这些代谢产物水平影响很小或使其降低。原型苯二氮卓类抗焦虑药氯氮卓,对所研究的每种代谢产物仅产生适度降低。非典型抗精神病药物氯氮平,使所研究的每种代谢产物水平升高,不过只有5 - HIAA效应出现在对行为无干扰的剂量下。氟哌啶醇(0.03 - 1.0毫克/千克)仅使受罚和未受罚反应降低,同时使MHPG、DOPAC和HVA水平升高;5 - HIAA水平相对未受影响。(摘要截断于250字)

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