Anaclet Christelle, Pedersen Nigel P, Ferrari Loris L, Venner Anne, Bass Caroline E, Arrigoni Elda, Fuller Patrick M
Division of Sleep Medicine, Department of Neurology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts 02215, USA.
Comprehensive Epilepsy Clinic, Department of Neurology, Beth Israel Deaconess Medical Center and Harvard Medical School, Boston, Massachusetts 02215, USA.
Nat Commun. 2015 Nov 3;6:8744. doi: 10.1038/ncomms9744.
Wakefulness, along with fast cortical rhythms and associated cognition, depend on the basal forebrain (BF). BF cholinergic cell loss in dementia and the sedative effect of anti-cholinergic drugs have long implicated these neurons as important for cognition and wakefulness. The BF also contains intermingled inhibitory GABAergic and excitatory glutamatergic cell groups whose exact neurobiological roles are unclear. Here we show that genetically targeted chemogenetic activation of BF cholinergic or glutamatergic neurons in behaving mice produced significant effects on state consolidation and/or the electroencephalogram but had no effect on total wake. Similar activation of BF GABAergic neurons produced sustained wakefulness and high-frequency cortical rhythms, whereas chemogenetic inhibition increased sleep. Our findings reveal a major contribution of BF GABAergic neurons to wakefulness and the fast cortical rhythms associated with cognition. These findings may be clinically applicable to manipulations aimed at increasing forebrain activation in dementia and the minimally conscious state.
觉醒,连同快速的皮质节律及相关认知,依赖于基底前脑(BF)。痴呆症中基底前脑胆碱能细胞的丧失以及抗胆碱能药物的镇静作用长期以来表明这些神经元对认知和觉醒很重要。基底前脑还包含相互交织的抑制性γ-氨基丁酸能(GABAergic)和兴奋性谷氨酸能细胞群,其确切的神经生物学作用尚不清楚。在这里,我们表明,在行为小鼠中对基底前脑胆碱能或谷氨酸能神经元进行基因靶向化学遗传激活,对状态巩固和/或脑电图产生了显著影响,但对总觉醒时间没有影响。基底前脑γ-氨基丁酸能神经元的类似激活产生了持续觉醒和高频皮质节律,而化学遗传抑制则增加了睡眠。我们的研究结果揭示了基底前脑γ-氨基丁酸能神经元对觉醒以及与认知相关的快速皮质节律的主要贡献。这些发现可能在临床上适用于旨在增加痴呆症和最低意识状态下前脑激活的操作。