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首页> 外文期刊>European Journal of Pharmacology: An International Journal >Psychostimulants affect dopamine transmission through both dopamine transporter-dependent and independent mechanisms
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Psychostimulants affect dopamine transmission through both dopamine transporter-dependent and independent mechanisms

机译:心理刺激剂通过多巴胺转运蛋白依赖性机制和独立机制影响多巴胺传递

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摘要

The precise mechanisms by which cocaine and amphetamine-like psychostimulants exert their reinforcing effects are not yet fully defined. It is widely believed, however, that these drugs produce their effects by enhancing dopamine neurotransmission in the brain, especially in limbic areas such as the nucleus accumbens, by inducing dopamine transporter-mediated reverse transport and/or blocking dopamine reuptake though the dopamine transporter. Here, we present the evidence that aside from dopamine transporter, non-dopamine transporter-mediated mechanisms also participate in psychostimulant-induced dopamine release and contribute to the behavioral effects of these drugs, such as locomotor activation and reward. Accordingly, psychostimulants could increase norepinephrine release in the prefrontal cortex, the latter then alters the firing pattern of dopamine neurons resulting in changes in action potential-dependent dopamine release. These alterations would further affect the temporal pattern of dopamine release in the nucleus accumbens, thereby modifying information processing in that area. Hence, a synaptic input to a nucleus accumbens neuron may be enhanced or inhibited by dopamine depending on its temporal relationship to dopamine release. Specific temporal patterns of dopamine release may also be required for certain forms of synaptic plasticity in the nucleus accumbens. Together, these effects induced by psychostimulants, mediated through a non-dopamine transporter-mediated mechanism involving norepinephrine and the prefrontal cortex, may also contribute importantly to the reinforcing properties of these drugs. (C) 2015 Elsevier B.V. All rights reserved.
机译:可卡因和类苯丙胺类精神兴奋剂发挥增强作用的确切机制尚未完全确定。然而,广泛认为,这些药物通过增强脑中多巴胺神经传递,特别是在伏隔核等边缘区域,通过诱导多巴胺转运蛋白介导的反向转运和/或阻止多巴胺转运蛋白对多巴胺的再摄取而产生作用。在这里,我们提供的证据表明,除了多巴胺转运蛋白外,非多巴胺转运蛋白介导的机制也参与了精神兴奋剂诱导的多巴胺释放,并有助于这些药物的行为效应,例如运动活化和奖励。因此,精神兴奋剂可以增加前额叶皮层中去甲肾上腺素的释放,然后后者改变多巴胺神经元的放电模式,从而导致动作电位依赖性多巴胺释放的变化。这些改变将进一步影响伏隔核中多巴胺释放的时间模式,从而改变该区域的信息处理。因此,多巴胺可以增强伏伏核神经元的突触输入,这取决于其与多巴胺释放的时间关系。对于伏隔核中某些形式的突触可塑性,也可能需要特定的多巴胺释放时间模式。精神刺激药通过非去甲肾上腺素和额叶前皮层的非多巴胺转运蛋白介导的机制介导的这些作用合在一起也可能对这些药物的增强特性起重要作用。 (C)2015 Elsevier B.V.保留所有权利。

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