Pfarr Simone, Meinhardt Marcus W, Klee Manuela L, Hansson Anita C, Vengeliene Valentina, Schönig Kai, Bartsch Dusan, Hope Bruce T, Spanagel Rainer, Sommer Wolfgang H
Institute of Psychopharmacology.
Institute of Psychopharmacology,
J Neurosci. 2015 Jul 29;35(30):10750-61. doi: 10.1523/JNEUROSCI.0684-15.2015.
Loss of control over drinking is a key deficit in alcoholism causally associated with malfunction of the medial prefrontal cortex (mPFC), but underlying molecular and cellular mechanisms remain unclear. Cue-induced reinstatement of alcohol seeking activates a subset of mPFC neurons in rats, identified by their common expression of the activity marker cFos and comprised of both principal and interneurons. Here, we used cFos-lacZ and pCAG-lacZ transgenic rats for activity-dependent or nonselective inactivation of neurons, respectively, which by their lacZ encoded β-galactosidase activity convert the inactive prodrug Daun02 into the neurotoxin daunorubicin. We report that activity-dependent ablation of a neuronal ensemble in the infralimbic but not the prelimbic subregion induced excessive alcohol seeking. The targeted neuronal ensemble was specific for the cue-induced response because stress-induced reinstatement was not affected in these animals. Importantly, nonselective inactivation of infralimbic neurons, using pCAG-lacZ rats, was without functional consequence on the cue-induced reinstatement task. Thus, inhibitory control over alcohol seeking is exerted by distinct functional ensembles within the infralimbic cortex rather than by a general inhibitory tone of this region on the behavioral output. This indicates a high level of functional compartmentation within the rat mPFC whereat many functional ensembles could coexist and interact within the same subregion.
Hebb's (1949) idea of memories as being represented in local neuronal networks is supported by identification of transiently stable activity patterns within subgroups of neurons. However, it is difficult to link individual networks to specific memory tasks, for example a learned behavior. By a novel approach of activity-dependent ablation, here we identify a specific neuronal ensemble located in the infralimbic subregion of the medial prefrontal cortex that controls a seeking response for alcohol in rats. Our data demonstrate that functional output depends on specific neuronal ensembles within a given brain region rather than on the global activity of that region, which raises important questions about the interpretation of numerous earlier experiments using site-directed silencing or stimulation for elucidating brain function.
饮酒失控是酒精中毒的一个关键缺陷,与内侧前额叶皮质(mPFC)功能障碍有因果关系,但其潜在的分子和细胞机制仍不清楚。线索诱导的觅酒行为恢复会激活大鼠mPFC中的一部分神经元,这些神经元共同表达活性标记物cFos,包括主神经元和中间神经元。在这里,我们分别使用cFos-lacZ和pCAG-lacZ转基因大鼠对神经元进行活性依赖性或非选择性失活,它们通过lacZ编码的β-半乳糖苷酶活性将无活性的前体药物道诺霉素转化为神经毒素柔红霉素。我们报告说,对边缘下而非边缘前亚区域的神经元集合进行活性依赖性消融会导致过度觅酒行为。靶向的神经元集合对线索诱导的反应具有特异性,因为在这些动物中,应激诱导的行为恢复不受影响。重要的是,使用pCAG-lacZ大鼠对边缘下神经元进行非选择性失活,对线索诱导的行为恢复任务没有功能影响。因此,对觅酒行为的抑制控制是由边缘下皮质内不同的功能集合施加的,而不是由该区域对行为输出的一般抑制性调节来实现的。这表明大鼠mPFC内存在高水平的功能分隔,其中许多功能集合可以在同一亚区域内共存并相互作用。
赫布(1949年)关于记忆在局部神经元网络中得以体现的观点,得到了神经元亚群中瞬时稳定活动模式的识别的支持。然而,很难将单个网络与特定的记忆任务联系起来,例如一种习得行为。通过一种新的活性依赖性消融方法,我们在此识别出位于内侧前额叶皮质边缘下亚区域的一个特定神经元集合,该集合控制大鼠的觅酒反应。我们的数据表明,功能输出取决于给定脑区内特定的神经元集合,而不是该区域的整体活动,这对许多早期使用定点沉默或刺激来阐明脑功能的实验的解释提出了重要问题。