Gao Ming, Liu Chang-Liang, Yang Shen, Jin Guo-Zhang, Bunney Benjamin S, Shi Wei-Xing
Department of Pharmacology, Shanghai Institute of Materia Medica, Shanghai Institutes of Biological Sciences, Chinese Academy of Sciences, Shanghai 201203, China.
J Neurosci. 2007 May 16;27(20):5414-21. doi: 10.1523/JNEUROSCI.5347-06.2007.
Stimulation of the prefrontal cortex (PFC) has been shown to have an excitatory influence on dopamine (DA) neurons. We report here that, under nonstimulated conditions, the activity of DA neurons in the ventral tegmental area (VTA) also covaries, on a subsecond timescale, with the activity of PFC cells. Thus, in 67% of VTA DA neurons recorded in chloral hydrate-anesthetized rats, the firing of the cell displayed a slow oscillation (SO) that was highly coherent with the activity of PFC neurons. The SO was suppressed by transections immediately caudal to the PFC or by intra-PFC infusion of tetrodotoxin, suggesting that it depends on inputs derived from the PFC. Unexpectedly, the SO in most VTA DA neurons was reversed in phase relative to PFC cell activity, suggesting that at least part of PFC information is transferred to DA neurons indirectly through inhibitory relay neurons. These results, together with those reported previously, suggest that the PFC can act through multiple pathways to exert both excitatory and inhibitory influences on DA neurons. The observed functional coupling between DA and PFC neurons further suggests that these pathways not only allow a bidirectional control of DA neurons by the PFC, but also enable action potential-dependent DA release to be coordinated, on a subsecond timescale, with glutamate release from PFC terminals. Further understanding of this coordinated activity may provide important new insights into brain functions and disorders thought to involve both VTA DA and PFC neurons.
前额叶皮层(PFC)的刺激已被证明对多巴胺(DA)神经元有兴奋性影响。我们在此报告,在非刺激条件下,腹侧被盖区(VTA)中DA神经元的活动在亚秒级时间尺度上也与PFC细胞的活动协同变化。因此,在水合氯醛麻醉的大鼠中记录的67%的VTA DA神经元中,细胞的放电表现出一种慢振荡(SO),它与PFC神经元的活动高度相干。SO被PFC尾侧紧邻处的横断或PFC内注入河豚毒素所抑制,这表明它依赖于来自PFC的输入。出乎意料的是,大多数VTA DA神经元中的SO相对于PFC细胞活动在相位上是相反的,这表明至少部分PFC信息是通过抑制性中继神经元间接传递给DA神经元的。这些结果与先前报道的结果一起表明,PFC可以通过多种途径对DA神经元施加兴奋性和抑制性影响。观察到的DA与PFC神经元之间的功能耦合进一步表明,这些途径不仅允许PFC对DA神经元进行双向控制,而且还能使动作电位依赖性DA释放与PFC终末的谷氨酸释放在亚秒级时间尺度上进行协调。对这种协调活动的进一步理解可能为涉及VTA DA和PFC神经元的脑功能和疾病提供重要的新见解。