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匹莫齐特在不同剂量及实验期间对大鼠辨别性杠杆释放行为的影响。

Effects of pimozide, across doses and within sessions, on discriminated lever release performance in rats.

作者信息

Skjoldager P, Fowler S C

机构信息

Department of Psychology, University of Mississippi, University 38677.

出版信息

Psychopharmacology (Berl). 1988;96(1):21-8. doi: 10.1007/BF02431528.

DOI:10.1007/BF02431528
PMID:3147474
Abstract

By using either water or food reinforcement, rats were trained to perform a discriminated lever release task (DLR), which required the rat to hold an operant lever in the closed position through one of five randomly presented foreperiods (2-6 s) and to release the lever within 0.5 s of the onset of a light discriminative stimulus. The procedure is analogous to the method used in human reaction time studies, except that here the procedure was free-operant, not fixed-trial. The effects of pimozide (0.12, 0.25, and 0.50 mg/kg) on this behavior were evaluated in terms of numbers of total responses, reinforced responses (successful releases), anticipatory responses, and extended responses (holding too long). Significant dose-dependent decreases in total responses and in reinforced responses were seen as supporting the hypothesis of a deficit in response initiation, which is often invoked to account for neuroleptic-induced reductions in discriminated active avoidance. Pimozide also increased the proportion of extended responses, suggesting that the drug affected the nature of responding as well as the tendency to respond. In the DLR task, pimozide produced substantial within-session decrements in both total responses and number of reinforced responses; however, extended responses exhibited within-session increases at the lowest dose. The results were discussed from both behavioral and pharmacological perspectives. The former emphasized motor effects and response initiation deficits, while the latter jointly considered neuronal responses to neuroleptic challenge and the dopamine release that results from behavioral activity itself.

摘要

通过使用水或食物强化,训练大鼠执行辨别性杠杆释放任务(DLR),该任务要求大鼠在五个随机呈现的前刺激期(2 - 6秒)中的一个期间内将操作杆保持在关闭位置,并在光辨别刺激开始后的0.5秒内释放杠杆。该程序类似于人类反应时间研究中使用的方法,不同之处在于这里的程序是自由操作的,而不是固定试验的。根据总反应次数、强化反应(成功释放)次数、预期反应次数和延长反应(保持时间过长)来评估匹莫齐特(0.12、0.25和0.50毫克/千克)对这种行为的影响。总反应次数和强化反应次数出现显著的剂量依赖性减少,这支持了反应启动缺陷的假设,该假设常被用来解释抗精神病药物引起的辨别性主动回避减少。匹莫齐特还增加了延长反应的比例,表明该药物不仅影响反应倾向,还影响反应的性质。在DLR任务中,匹莫齐特在整个实验过程中使总反应次数和强化反应次数都大幅减少;然而,在最低剂量下,延长反应在整个实验过程中有所增加。从行为学和药理学角度对结果进行了讨论。前者强调运动效应和反应启动缺陷,而后者则共同考虑神经元对抗精神病药物刺激的反应以及行为活动本身引起的多巴胺释放。

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1
Effects of pimozide, across doses and within sessions, on discriminated lever release performance in rats.匹莫齐特在不同剂量及实验期间对大鼠辨别性杠杆释放行为的影响。
Psychopharmacology (Berl). 1988;96(1):21-8. doi: 10.1007/BF02431528.
2
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本文引用的文献

1
EFFECTS OF DRUGS ON AVOIDANCE AND ESCAPE BEHAVIOR.药物对回避和逃避行为的影响。
Fed Proc. 1964 Jul-Aug;23:818-35.
2
An analysis of chlorpromazine-induced suppression of the avoidance response.氯丙嗪诱导的回避反应抑制分析。
Psychopharmacologia. 1962 Oct 31;3:361-73. doi: 10.1007/BF00408321.
3
Use of operant response duration to distinguish the effects of haloperidol from nonreward.
Pharmacol Biochem Behav. 1981 Aug;15(2):327-9. doi: 10.1016/0091-3057(81)90196-9.
Psychopharmacology (Berl). 2009 Jan;201(4):601-9. doi: 10.1007/s00213-008-1328-z. Epub 2008 Sep 17.
4
Distinguishing between haloperidol's and decamethonium's disruptive effects on operant behavior in rats: use of measurements that complement response rate.区分氟哌啶醇和十烃季铵对大鼠操作性行为的干扰作用:使用补充反应率的测量方法。
J Exp Anal Behav. 1991 Sep;56(2):239-60. doi: 10.1901/jeab.1991.56-239.
5
Different patterns of behavior produced by haloperidol, pentobarbital, and dantrolene in tests of unconditioned locomotion and operant responding.氟哌啶醇、戊巴比妥和丹曲林在非条件运动和操作性反应测试中产生的不同行为模式。
Psychopharmacology (Berl). 1991;104(2):150-6. doi: 10.1007/BF02244170.
6
Scopolamine attenuates the motor disruptions but not the attentional disturbances induced by haloperidol in a sustained attention task in the rat.在大鼠的持续注意力任务中,东莨菪碱可减轻氟哌啶醇引起的运动障碍,但不能减轻其引起的注意力障碍。
Psychopharmacology (Berl). 1991;105(1):93-100. doi: 10.1007/BF02316869.
4
Effects of aerobic training on reactive capacity: an animal model.有氧运动训练对反应能力的影响:动物模型
J Gerontol. 1981 Nov;36(6):654-62. doi: 10.1093/geronj/36.6.654.
5
Time course of chronic haloperidol and clozapine upon operant rate and duration.
Eur J Pharmacol. 1981 Mar 5;70(1):65-70. doi: 10.1016/0014-2999(81)90433-7.
6
Morphine versus haloperidol catalepsy in the rat: a behavioral analysis of postural support mechanisms.大鼠中吗啡与氟哌啶醇致僵住症的比较:姿势支持机制的行为分析
Brain Res. 1980 Nov 10;201(1):143-72. doi: 10.1016/0006-8993(80)90781-7.
7
Avoidance performance, cue and response-choice discrimination after neuroleptic treatment.
Pharmacol Biochem Behav. 1982 Dec;17(6):1245-9. doi: 10.1016/0091-3057(82)90128-9.
8
Failure to obtain functional equivalence between dopamine receptor blockade and extinction: evidence supporting a sensory-motor conditioning hypothesis.未能在多巴胺受体阻断与消退之间获得功能等效性:支持感觉运动条件作用假说的证据。
Pharmacol Biochem Behav. 1982 Jan;16(1):67-72. doi: 10.1016/0091-3057(82)90015-6.
9
Voltammetry in unanesthetized rat: increases of striatal dopamine turnover after unilateral haloperidol injection into the substantia nigra.未麻醉大鼠的伏安法:向黑质单侧注射氟哌啶醇后纹状体多巴胺周转率增加。
Neurosci Lett. 1984 Sep 7;50(1-3):263-7. doi: 10.1016/0304-3940(84)90496-8.
10
Speed of movement initiation performance predicts differences in [3H]spiroperidol receptor binding in normal rats.运动起始表现的速度可预测正常大鼠中[³H]螺哌啶醇受体结合的差异。
Psychopharmacology (Berl). 1984;83(2):205-9. doi: 10.1007/BF00429736.