Department of Physiology, University of Arizona, Tucson, AZ, USA.
Department of Chemistry and Biochemistry, University of Arizona, Tucson, AZ, USA.
Brain Stimul. 2018 Mar-Apr;11(2):426-434. doi: 10.1016/j.brs.2017.11.010. Epub 2017 Nov 15.
The medial prefrontal cortex (mPFC) coordinates goal-directed behaviors, which may be mediated through mPFC regulation of dopamine release in the nucleus accumbens (NAc). Furthermore, frequency-specific oscillatory activity between the frontal cortex and downstream structures may facilitate inter-region communication. Although high-frequency (e.g., 60 Hz) mPFC stimulation is known to increase basal dopamine levels in the NAc, little is known about how phasic dopamine release is affected by mPFC stimulation. Understanding the frequency-specific control of phasic dopamine release by mPFC stimulation could elucidate mechanisms by which the mPFC modulates other regions. It could also inform optimization of deep brain stimulation for treatment of neurological disorders.
The goal of this work was to characterize the frequency response of NAc dopamine release resultant from mPFC stimulation. We hypothesized that the magnitude of dopamine release in the NAc would increase with increasing stimulation frequency.
Electrical stimulation of the mPFC of anesthetized rats was delivered at 4-60 Hz and at varying durations while measuring NAc dopamine release with fast-scan cyclic voltammetry.
mPFC stimulation resulted in phasic dopamine release in the NAc. Furthermore, 20 Hz stimulation evoked the largest peak response for stimulation intervals >5 s when compared to higher or lower frequencies.
Activation of the mPFC drives dopamine release in the NAc in a complex frequency- and duration-dependent manner. This has implications for the use of deep brain stimulation treatment of disorders marked by dopaminergic dysregulation, and suggest that mPFC may exert more specialized control over neuromodulator release than previously understood.
内侧前额叶皮层 (mPFC) 协调有目的的行为,这可能通过 mPFC 调节伏隔核 (NAc) 中的多巴胺释放来介导。此外,前额叶皮层和下游结构之间的频域特异性振荡活动可能促进区域间的通讯。虽然已知高频(例如 60 Hz)mPFC 刺激会增加 NAc 中的基础多巴胺水平,但对于 mPFC 刺激如何影响相位多巴胺释放知之甚少。了解 mPFC 刺激对相位多巴胺释放的频域特异性控制可以阐明 mPFC 调节其他区域的机制。它还可以为优化深部脑刺激治疗神经障碍提供信息。
这项工作的目标是描述 mPFC 刺激引起的 NAc 多巴胺释放的频率响应。我们假设 NAc 中的多巴胺释放量会随着刺激频率的增加而增加。
在麻醉大鼠中,在 4-60 Hz 的频率下以不同的持续时间进行 mPFC 电刺激,同时使用快速扫描循环伏安法测量 NAc 多巴胺释放。
mPFC 刺激导致 NAc 中的相位多巴胺释放。此外,与更高或更低频率相比,20 Hz 刺激在刺激间隔>5 s 时产生最大的峰响应。
mPFC 的激活以复杂的频率和持续时间依赖方式驱动 NAc 中的多巴胺释放。这对使用深部脑刺激治疗多巴胺能失调为特征的疾病有影响,并表明 mPFC 可能对神经调质释放施加比以前理解的更专门的控制。