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喹哌嗪对猫的行为影响。

Behavioral effects of quipazine in the cat.

作者信息

Trulson M E, Brandstetter J W, Crisp T, Jacobs B L

出版信息

Eur J Pharmacol. 1982 Mar 12;78(3):295-305. doi: 10.1016/0014-2999(82)90031-0.

Abstract

Administration of quipazine to cats elicits a number of behaviors, such as limb flicking abortive grooming, investigatory behavior and hallucinatory-like behavior, which we have previously proposed as an animal behavioral model for studying the actions of LSD and related hallucinogens. While recent studies have indicated that these model behaviors may not be totally specific for hallucinogenic drugs, the model can still be useful for studying drug action. Quipazine (0.5-5.0 mg/kg i.p.) produced significant increases in limb flicking, abortive grooming, investigatory behavior, hallucinatory-like behavior grooming, head and body shakes, staring and yawning. These behavioral changes persisted for 1-6 h, depending on the dose of quipazine employed. Administration of quipazine (5.0 mg/kg per day) for 5 consecutive days produced no significant tolerance effect on any of these model behaviors. These quipazine induced behavioral changes were potentiated by pretreatment with apomorphine, and partially blocked by pretreatment with haloperidol. Quipazine-induced behavioral changes were potentiated by prior serotonin depletion with p-chlorophenylalanine, and completely blocked by pretreatment with a monoamine oxidase inhibitor or the serotonin precursor, L-5-hydroxytryptophan. These quipazine-induced behavioral changes were also blocked by pretreatment with the serotonin receptor blockers, cinnanserin, methysergide or cyproheptadine. The mechanism of action of quipazine, as well as the neuropharmacology of the limb flick model, is discussed in the content of these studies with serotonergic and dopaminergic drugs.

摘要

给猫注射喹哌嗪会引发多种行为,如肢体轻弹、无效梳理、探究行为和类似幻觉的行为,我们之前已将其作为一种动物行为模型,用于研究麦角酸二乙酰胺(LSD)及相关致幻剂的作用。虽然最近的研究表明,这些模型行为可能并非完全特异于致幻药物,但该模型仍可用于研究药物作用。喹哌嗪(腹腔注射0.5 - 5.0毫克/千克)可显著增加肢体轻弹、无效梳理、探究行为、类似幻觉的行为梳理、头部和身体抖动、凝视和打哈欠。这些行为变化持续1 - 6小时,具体取决于所使用的喹哌嗪剂量。连续5天每天注射喹哌嗪(5.0毫克/千克)对任何这些模型行为均未产生显著的耐受性影响。阿扑吗啡预处理可增强喹哌嗪诱导产生的这些行为变化,而氟哌啶醇预处理则可部分阻断这些变化。用对氯苯丙氨酸使血清素耗竭后,喹哌嗪诱导的行为变化会增强,而用单胺氧化酶抑制剂或血清素前体L - 5 - 羟色氨酸预处理则可完全阻断这些变化。血清素受体阻滞剂肉桂硫胺、甲基麦角新碱或赛庚啶预处理也可阻断喹哌嗪诱导的这些行为变化。在这些使用血清素能和多巴胺能药物的研究中,讨论了喹哌嗪的作用机制以及肢体轻弹模型的神经药理学。

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