Lambert Peter M, Salvatore Sofia V, Lu Xinguo, Shu Hong-Jin, Benz Ann, Rensing Nicholas, Yuede Carla M, Wong Michael, Zorumski Charles F, Mennerick Steven
Department of Psychiatry, Washington University in St. Louis School of Medicine, St. Louis, Missouri 63110.
Medical Scientist Training Program, Washington University in St. Louis School of Medicine, St. Louis, Missouri 63110.
J Neurosci. 2025 May 14;45(20):e0601242025. doi: 10.1523/JNEUROSCI.0601-24.2025.
GABA receptors containing δ subunits have been shown to mediate tonic/slow inhibition in the CNS. These receptors are typically found extrasynaptically and are activated by relatively low levels of ambient GABA in the extracellular space. In the mouse neocortex, δ subunits are expressed by some pyramidal cells as well as on parvalbumin-positive (PV+) interneurons. An important function of PV+ interneurons is the organization of coordinated network activity that can be measured by EEG. However, it remains unclear what role tonic/slow inhibitory control of PV+ neurons may play in shaping oscillatory activity. After validating expected functional loss of δ-associated current in cortex of PV δcKO mice of both sexes, we performed EEG recordings to survey network activity across wake and sleep states. PV δcKO mice showed altered spectral content of EEG during NREM and REM sleep that was a result of increased oscillatory activity in NREM and the emergence of transient high-amplitude bursts of theta-frequency activity during REM. Viral reintroduction of to PV+ interneurons in PV δcKO mice rescued REM EEG phenotypes, supporting an important role for δ subunit-mediated inhibition of PV+ interneurons for maintaining normal REM cortical oscillations.
含有δ亚基的GABA受体已被证明可介导中枢神经系统中的紧张性/缓慢抑制。这些受体通常在突触外被发现,并被细胞外空间中相对较低水平的周围GABA激活。在小鼠新皮层中,一些锥体细胞以及小白蛋白阳性(PV+)中间神经元表达δ亚基。PV+中间神经元的一个重要功能是组织可通过脑电图测量的协调网络活动。然而,尚不清楚PV+神经元的紧张性/缓慢抑制控制在塑造振荡活动中可能起什么作用。在验证了两性PV δcKO小鼠皮层中与δ相关电流的预期功能丧失后,我们进行了脑电图记录,以调查清醒和睡眠状态下的网络活动。PV δcKO小鼠在非快速眼动(NREM)和快速眼动(REM)睡眠期间脑电图的频谱内容发生了改变,这是由于NREM期间振荡活动增加以及REM期间出现θ频率活动的短暂高振幅爆发所致。在PV δcKO小鼠中,将病毒重新导入PV+中间神经元可挽救REM脑电图表型,支持δ亚基介导的对PV+中间神经元的抑制在维持正常REM皮层振荡中的重要作用。