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d-麦角酸二乙酰胺(LSD)、2,5-二甲氧基-4-甲基苯丙胺(DOM)和d-苯丙胺对正常及6-羟基多巴胺处理大鼠操作性反应的影响。

The effects of d-lysergic acid diethylamide (LSD), 2,5-dimethoxy-4-methylamphetamine (DOM) and d-amphetamine on operant responding in control and 6-hydroxydopamine-treated rats.

作者信息

Commissaris R, Lyness W H, Cordon J J, Moore K E, Rech R H

出版信息

Pharmacol Biochem Behav. 1980 Nov;13(5):621-6. doi: 10.1016/0091-3057(80)90002-7.

DOI:10.1016/0091-3057(80)90002-7
PMID:7443731
Abstract

The purpose of the present study was to determine the role of central catecholaminergic neuronal systems in the effects of LSD, DOM and d-amphetamine on fixed ratio (FR) operant responding in rats. Food-deprived male rats were trained to press a bar for food reinforcement on a FR-40 schedule. Control responding on this schedule is characterized by a rapid, constant rate of responding (approximately 100 responses/min) throughout a 40 min test session. LSD and DOM, as with other hallucinogens, produced dose-dependent periods of nonresponding or "pausing," followed by reinstatement of responding at or near the control rate. Administration of the non-hallucinogen, d-amphetamine, did not produce "pausing," but caused the response rate to slow and become erratic. In animals pretreated intraventricularly with 6-hydroxydopamine (6-OHDA; 200 micrograms/10 microliter X 2), the response to LSD and DOM was unchanged, while the response to d-amphetamine was significantly diminished. The neurotoxin significantly decreased brain catecholamines to less than 25 percent of control in al regions examined, without altering 5-HT concentrations in these same regions. These data demonstrate that the effects of LSD and DOM on FR-40 responding are quite different from those of d-amphetamine, and that this difference may be due to the extent of catecholamine involvement in the effects of these agents.

摘要

本研究的目的是确定中枢儿茶酚胺能神经元系统在麦角酸二乙胺(LSD)、2,5-二甲氧基-4-甲基苯丙胺(DOM)和右旋苯丙胺对大鼠固定比率(FR)操作性反应的影响中所起的作用。将禁食的雄性大鼠训练在FR-40程序下按压杠杆以获取食物强化。在此程序下的对照反应的特征是在整个40分钟的测试过程中反应速度快速且恒定(约100次反应/分钟)。与其他致幻剂一样,LSD和DOM产生剂量依赖性的无反应期或“暂停”期,随后以接近对照速度恢复反应。给予非致幻剂右旋苯丙胺不会产生“暂停”,但会导致反应速度减慢并变得不稳定。在脑室内预先用6-羟基多巴胺(6-OHDA;200微克/10微升×2)处理的动物中,对LSD和DOM的反应未改变,而对右旋苯丙胺的反应显著减弱。这种神经毒素使所检查的所有区域的脑儿茶酚胺显著降低至对照的25%以下,而这些相同区域的5-羟色胺浓度未改变。这些数据表明,LSD和DOM对FR-40反应的影响与右旋苯丙胺的影响有很大不同,这种差异可能是由于儿茶酚胺参与这些药物作用的程度不同所致。

相似文献

1
The effects of d-lysergic acid diethylamide (LSD), 2,5-dimethoxy-4-methylamphetamine (DOM) and d-amphetamine on operant responding in control and 6-hydroxydopamine-treated rats.d-麦角酸二乙酰胺(LSD)、2,5-二甲氧基-4-甲基苯丙胺(DOM)和d-苯丙胺对正常及6-羟基多巴胺处理大鼠操作性反应的影响。
Pharmacol Biochem Behav. 1980 Nov;13(5):621-6. doi: 10.1016/0091-3057(80)90002-7.
2
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Enhancement of the behavioral effects of 2,5-dimethoxy-4-methyl-amphetamine (DOM) by pretreatment with p-chlorophenylalanine.对氯苯丙氨酸预处理增强2,5-二甲氧基-4-甲基苯丙胺(DOM)的行为效应
Pharmacol Biochem Behav. 1980 Oct;13(4):605-8. doi: 10.1016/0091-3057(80)90290-7.
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Stereoselective effects of 1-(2,5-dimethoxy-4-methylphenyl)-2-aminopropane (DOM) on schedule-controlled behavior.1-(2,5-二甲氧基-4-甲基苯基)-2-氨基丙烷(DOM)对程序控制行为的立体选择性作用。
Pharmacol Biochem Behav. 1977 Oct;7(4):307-10. doi: 10.1016/0091-3057(77)90225-8.
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Naloxone alters the effects of LSD, DOM and quipazine on operant behavior of rats.纳洛酮会改变麦角酸二乙酰胺、2,5-二甲氧基-4-甲基苯丙胺和喹哌嗪对大鼠操作性行为的影响。
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Neurotransmitter basis of the behavioral effects of hallucinogens.致幻剂行为效应的神经递质基础。
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Central 5-hydroxytryptamine and the effects of hallucinogens and phenobarbital on operant responding in rats.中枢5-羟色胺以及致幻剂和苯巴比妥对大鼠操作性反应的影响。
Pharmacol Biochem Behav. 1981 May;14(5):595-601. doi: 10.1016/0091-3057(81)90118-0.
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Behavioral and neuropharmacological analysis of amphetamine and 2,5-dimethoxy-4-methylamphetamine in rats.大鼠中苯丙胺和2,5-二甲氧基-4-甲基苯丙胺的行为和神经药理学分析。
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MDA and DOM: substituted amphetamines that do not produce amphetamine-like discriminative stimuli in the rat.MDA和DOM:在大鼠中不会产生类似苯丙胺辨别刺激效应的取代苯丙胺类物质。
Psychopharmacology (Berl). 1980;67(3):311-2. doi: 10.1007/BF00431274.
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LSD and d-amphetamine effects on fixed interval responding in the rat.麦角酸二乙酰胺(LSD)和右旋苯丙胺对大鼠固定间隔反应的影响。
Pharmacol Biochem Behav. 1977 Mar;6(3):269-72. doi: 10.1016/0091-3057(77)90025-9.

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