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首页> 外文期刊>Neuroscience: An International Journal under the Editorial Direction of IBRO >Effects of dopamine depletion in the medial prefrontal cortex on the stress-induced increase in extracellular dopamine in the nucleus accumbens core and shell.
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Effects of dopamine depletion in the medial prefrontal cortex on the stress-induced increase in extracellular dopamine in the nucleus accumbens core and shell.

机译:内侧前额叶皮层中多巴胺的消耗对伏隔核核心和壳中应激诱导的细胞外多巴胺增加的影响。

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In the present study we examined whether depletion of dopamine in the medial prefrontal cortex alters the neurochemical activity of mesoaccumbens dopamine neurons and/or their behavioral correlate, motor behavior. Infusion of 6-hydroxydopamine (1 microgram) into the medial prefrontal cortex of rats pretreated with a norepinephrine uptake blocker produced a 70% loss of tissue dopamine, with relative sparing of the norepinephrine content (-23%) in that region. Using in vivo microdialysis, we monitored basal and evoked extracellular dopamine in the nucleus accumbens core and shell of control and lesioned rats. The concentration of basal extracellular dopamine in the nucleus accumbens core was similar in control and lesioned rats; however, basal dopamine efflux in the nucleus accumbens shell was approximately 30% higher in lesioned rats than in controls. Lesions did not alter the ability of systemic D-amphetamine (1.5 mg/kg, i.p.) to increase extracellular dopamine in the nucleus accumbens shell, in contrast, the dopamine depletion in the medial prefrontal cortex attenuated the amphetamine-induced increase in extracellular dopamine in the nucleus accumbens core, as well as the amphetamine-induced increase in locomotor activity. Lesions did not significantly alter the effects of tail pressure (30 min) on extracellular dopamine in the nucleus accumbens core. However, the depletion of dopamine in the medial prefrontal cortex potentiated the stress-induced increase in extracellular dopamine in the nucleus accumbens shell. These data demonstrate that mesocortical dopamine neurons influence (i) amphetamine-induced dopamine efflux in the nucleus accumbens core and (ii) stress-evoked dopamine efflux in the nucleus accumbens shell. It has been proposed that a disruption in the interaction between cortical and subcortical dopamine neurons is involved in the pathophysiology of schizophrenia. The present data raise the possibility that a disruption in the interaction between mesocortical dopamine neurons and dopamine neurons projecting to the nucleus accumbens shell is involved in those symptoms of schizophrenia that are influenced by stress.
机译:在本研究中,我们检查了内侧前额叶皮层中多巴胺的消耗是否改变了中隔累积多巴胺神经元的神经化学活性和/或它们的行为相关性,运动行为。在用去甲肾上腺素摄取阻滞剂预处理的大鼠的内侧前额叶皮质中注入6-羟基多巴胺(1微克)会导致组织多巴胺损失70%,而该区域中去甲肾上腺素的含量相对较少(-23%)。使用体内微透析,我们监测伏隔核和对照组和病变大鼠的核的核和壳中的基础和诱发的细胞外多巴胺。对照组和病变大鼠的伏伏核核心中的基础细胞外多巴胺浓度相似。然而,病变大鼠的伏隔核壳中的基础多巴胺流出量比对照组高约30%。病变并未改变全身D-苯丙胺(1.5 mg / kg,ip)增加伏伏核壳中细胞外多巴胺的能力,相比之下,内侧前额叶皮层中的多巴胺消耗减弱了苯丙胺诱导的伏安中诱导的细胞外多巴胺增加。伏隔核核心以及苯丙胺诱导的运动活动增加。病变并未明显改变尾压(30分钟)对伏伏核核心中细胞外多巴胺的影响。然而,内侧前额叶皮层中多巴胺的消耗增强了伏隔核壳中应激诱导的细胞外多巴胺的增加。这些数据表明中皮层多巴胺神经元影响(i)苯丙胺诱导伏隔核核心中的多巴胺流出和(ii)应力诱发多巴胺伏核中的多巴胺流出。已经提出,精神分裂症的病理生理学涉及皮层和皮层下多巴胺神经元之间相互作用的破坏。目前的数据提出了中皮层多巴胺神经元和投射到伏隔核壳的多巴胺神经元之间相互作用的破坏参与受压力影响的精神分裂症症状的可能性。

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