咖啡因通过抑制腺苷抑制可卡因诱导的多巴胺释放。

Lauren B Malave, Patricia A Broderick
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引用次数: 16

摘要

背景:众所周知,可卡因成瘾的强化特性是由大脑奖赏区多巴胺(DA)的急剧增加引起的。然而,据推测,其他机制有助于增加。腺苷是一个与睡眠-觉醒周期相关的系统,在调节神经元活动方面最重要。因此,越来越多的证据指向其参与调节DA的释放。目前的研究旨在检测腺苷在可卡因诱导的DA释放中的作用。方法:使用增加剂量的可卡因、咖啡因及其组合,以及8-环戊基茶碱(CPT),一种腺苷A1拮抗剂(单独使用和与可卡因联合使用)来表示反应曲线。一种新型生物传感器BRODERICK PROBE®植入伏隔核,在自由运动的动物体内实时成像药物诱导的DA释放激增。结果:低剂量组(2.5 mg/kg可卡因和12.5 mg/kg咖啡因)和高剂量组(10 mg/kg可卡因和50 mg/kg咖啡因)对DA的释放有抑制作用,提示有神经保护作用。同样,CPT和可卡因联合使用时,DA激增减少。因此,低剂量和高剂量的非选择性腺苷拮抗剂咖啡因和中等剂量的选择性腺苷拮抗剂CPT可以防止可卡因诱导的DA释放。结论:这些结果表明腺苷和DA释放之间存在显著的相互作用,并为可卡因成瘾和与DA功能障碍相关的疾病提供了治疗选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Caffeine's Attenuation of Cocaine-Induced Dopamine Release by Inhibition of Adenosine.

Caffeine's Attenuation of Cocaine-Induced Dopamine Release by Inhibition of Adenosine.

Caffeine's Attenuation of Cocaine-Induced Dopamine Release by Inhibition of Adenosine.

Caffeine's Attenuation of Cocaine-Induced Dopamine Release by Inhibition of Adenosine.

Background: It is well known that the reinforcing properties of cocaine addiction are caused by the sharp increase of dopamine (DA) in the reward areas of the brain. However, other mechanisms have been speculated to contribute to the increase. Adenosine is one system that is associated with the sleep-wake cycle and is most important in regulating neuronal activity. Thus, more and more evidence is pointing to its involvement in regulating DA release. The current study set out to examine the role of adenosine in cocaine-induced DA release. Methods: Increasing doses of cocaine, caffeine, and their combination, as well as, 8-cyclopentyltheophylline (CPT), an adenosine A1 antagonist (alone and in combination with cocaine) were used to denote a response curve. A novel biosensor, the BRODERICK PROBE® was implanted in the nucleus accumbens to image the drug-induced surge of DA release in vivo, in the freely moving animal in real time. Results: Combinations of cocaine and caffeine were observed to block the increased release of DA moderately after administration of the low dose (2.5 mg/kg cocaine and 12.5 mg/kg caffeine) and dramatically after administration of the high dose (10 mg/kg cocaine and 50 mg/kg caffeine), suggesting neuroprotection. Similarly, CPT and cocaine showed a decreased DA surge when administered in combination. Thus, the low and high dose of a nonselective adenosine antagonist, caffeine, and a moderate dose of a selective adenosine antagonist, CPT, protected against the cocaine-induced DA release. Conclusions: These results show a significant interaction between adenosine and DA release and suggest therapeutic options for cocaine addiction and disorders associated with DA dysfunction.

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