Seo Dong-Oh, Funderburk Samuel C, Bhatti Dionnet L, Motard Laura E, Newbold Dillan, Girven Kasey S, McCall Jordan G, Krashes Michael, Sparta Dennis R, Bruchas Michael R
Department of Anesthesiology, Division of Basic Research.
Diabetes, Endocrinology and Obesity Branch, National Institutes of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland 20892, and.
J Neurosci. 2016 Oct 19;36(42):10831-10842. doi: 10.1523/JNEUROSCI.1164-16.2016.
The neural circuitry underlying mammalian reward behaviors involves several distinct nuclei throughout the brain. It is widely accepted that the midbrain dopamine (DA) neurons are critical for the reward-related behaviors. Recent studies have shown that the centromedial nucleus of the amygdala (CeMA) has a distinct role in regulating reward-related behaviors. However, the CeMA and ventromedial PFC (vmPFC) interaction in reward regulation remains poorly understood. Here, we identify and dissect a GABAergic projection that originates in the CeMA and terminates in the vmPFC (VGat-Cre) using viral-vector-mediated, cell-type-specific optogenetic techniques in mice. Pathway-specific optogenetic activation of the VGat-Cre circuit in awake, behaving animals produced a positive, reward-like phenotype in real-time place preference and increased locomotor activity in open-field testing. In sucrose operant conditioning, the photoactivation of these terminals increased nose-poking effort with no effect on licking behavior and robustly facilitated the extinction of operant behavior. However, photoactivation of these terminals did not induce self-stimulation in the absence of an external reward. The results described here suggest that the VGat-Cre projection acts to modulate existing reward-related behaviors.
Many studies have shown that the interactions between the centromedial nucleus of the amygdala (CeMA) and ventromedial PFC (vmPFC) have critical roles for emotional regulation. However, most studies have associated this circuit with fear and anxiety behaviors and emphasized top-down processing from vmPFC to CeMA. Here, we provide new evidence for bottom-up CeMA to vmPFC influence on reward-related behaviors. Although previous work implicated the CeMA in incentive salience, our results isolate the investigation to a specific CeMA GABAergic projection to the vmPFC. This long-range GABAergic interaction between amygdala and frontal cortex adds a new dimension to the complex regulation of reward-related behaviors.
哺乳动物奖赏行为背后的神经回路涉及大脑中几个不同的核团。中脑多巴胺(DA)神经元对奖赏相关行为至关重要,这一点已被广泛接受。最近的研究表明,杏仁核中央内侧核(CeMA)在调节奖赏相关行为中具有独特作用。然而,CeMA与腹内侧前额叶皮质(vmPFC)在奖赏调节中的相互作用仍知之甚少。在此,我们利用病毒载体介导的细胞类型特异性光遗传学技术,在小鼠中识别并剖析了一条起源于CeMA并终止于vmPFC的GABA能投射通路(VGat-Cre)。在清醒、活动的动物中,对VGat-Cre回路进行通路特异性光遗传学激活,在实时位置偏好实验中产生了积极的、类似奖赏的表型,并在旷场测试中增加了运动活性。在蔗糖操作性条件反射实验中,这些终末的光激活增加了戳鼻努力,对舔舐行为没有影响,并有力地促进了操作性行为的消退。然而,在没有外部奖赏的情况下,这些终末的光激活并未诱导自我刺激。此处描述的结果表明,VGat-Cre投射起到调节现有奖赏相关行为的作用。
许多研究表明,杏仁核中央内侧核(CeMA)与腹内侧前额叶皮质(vmPFC)之间的相互作用对情绪调节至关重要。然而,大多数研究将该回路与恐惧和焦虑行为相关联,并强调从vmPFC到CeMA的自上而下的加工过程。在此,我们提供了新的证据,证明从CeMA到vmPFC的自下而上的影响对奖赏相关行为的作用。尽管先前的研究表明CeMA参与动机显著性,但我们的结果将研究聚焦于CeMA到vmPFC的特定GABA能投射。杏仁核与额叶皮质之间这种长距离的GABA能相互作用为奖赏相关行为的复杂调节增添了新的维度。