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西酞普兰增强可卡因对大鼠的主观效应。

Citalopram enhances cocaine's subjective effects in rats.

作者信息

Soto Paul L, Hiranita Takato, Katz Jonathan L

机构信息

Behavioral Biology Research Center, Johns Hopkins University, Baltimore, Maryland 21224-6823, USA.

出版信息

Behav Pharmacol. 2009 Dec;20(8):759-62. doi: 10.1097/FBP.0b013e328333a267.

Abstract

Serotonin-selective reuptake inhibitors (SSRIs) have been shown to enhance the locomotor stimulatory, discriminative-stimulus, and convulsive effects of cocaine in rodents. A pharmacokinetic mechanism for the interaction is supported by increases in the brain levels of cocaine by fluoxetine treatment. Furthermore, the locomotor-stimulant effects of cocaine in rodents are enhanced by fluoxetine and fluvoxamine, SSRIs known to inhibit cocaine-metabolizing cytochrome P450 enzymes, whereas citalopram, an SSRI that does not inhibit P450 enzymes, does not enhance cocaine's locomotor-stimulant effects. Citalopram, however, attenuated the discriminative-stimulus effects of cocaine in squirrel monkeys trained to discriminate cocaine from saline, though it enhanced the discriminative-stimulus effects of a low dose of cocaine in rats trained to discriminate high and low doses of the drug. This study investigated the effects of citalopram on cocaine's discriminative-stimulus effects in rats trained more simply to discriminate cocaine from saline. Citalopram alone produced predominantly saline-appropriate responding, but when administered before cocaine, citalopram dose-dependently shifted the cocaine dose-response curve leftward. The present findings suggest that enhancement of cocaine's discriminative-stimulus effects may occur through a mechanism different from that underlying enhancement of cocaine's locomotor effects or that another action of citalopram selectively blocks locomotor enhancement.

摘要

血清素选择性再摄取抑制剂(SSRIs)已被证明可增强可卡因对啮齿动物的运动刺激、辨别刺激和惊厥作用。氟西汀治疗可提高大脑中可卡因的水平,这支持了两者相互作用的药代动力学机制。此外,已知抑制可卡因代谢细胞色素P450酶的SSRIs氟西汀和氟伏沙明可增强可卡因对啮齿动物的运动刺激作用,而不抑制P450酶的SSRI西酞普兰则不会增强可卡因的运动刺激作用。然而,西酞普兰减弱了经训练可区分可卡因和生理盐水的松鼠猴对可卡因的辨别刺激作用,尽管它增强了经训练可区分高剂量和低剂量可卡因的大鼠对低剂量可卡因的辨别刺激作用。本研究调查了西酞普兰对经更简单训练以区分可卡因和生理盐水的大鼠中可卡因辨别刺激作用的影响。单独使用西酞普兰主要产生与生理盐水相符的反应,但在给予可卡因之前给药时,西酞普兰会使可卡因剂量反应曲线剂量依赖性地向左移动。目前的研究结果表明,可卡因辨别刺激作用的增强可能通过与可卡因运动作用增强不同的机制发生,或者西酞普兰的另一种作用选择性地阻断了运动增强。

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