Butler James L, Mendonça Philipe R F, Robinson Hugh P C, Paulsen Ole
Department of Physiology, Development and Neuroscience, University of Cambridge, Physiological Laboratory, Cambridge CB2 3EG, United Kingdom.
Department of Physiology, Development and Neuroscience, University of Cambridge, Physiological Laboratory, Cambridge CB2 3EG, United Kingdom
J Neurosci. 2016 Apr 13;36(15):4155-69. doi: 10.1523/JNEUROSCI.3150-15.2016.
Gamma oscillations (30-120 Hz) are thought to be important for various cognitive functions, including perception and working memory, and disruption of these oscillations has been implicated in brain disorders, such as schizophrenia and Alzheimer's disease. The cornu ammonis area 1 (CA1) of the hippocampus receives gamma frequency inputs from upstream regions (cornu ammonis area 3 and medial entorhinal cortex) and generates itself a faster gamma oscillation. The exact nature and origin of the intrinsic CA1 gamma oscillation is still under debate. Here, we expressed channel rhodopsin-2 under the CaMKIIα promoter in mice and prepared hippocampal slices to produce a model of intrinsic CA1 gamma oscillations. Sinusoidal optical stimulation of CA1 at theta frequency was found to induce robust theta-nested gamma oscillations with a temporal and spatial profile similar to CA1 gamma in vivo The results suggest the presence of a single gamma rhythm generator with a frequency range of 65-75 Hz at 32 °C. Pharmacological analysis found that the oscillations depended on both AMPA and GABAA receptors. Cell-attached and whole-cell recordings revealed that excitatory neuron firing slightly preceded interneuron firing within each gamma cycle, suggesting that this intrinsic CA1 gamma oscillation is generated with a pyramidal-interneuron circuit mechanism.
This study demonstrates that the cornu ammonis area 1 (CA1) is capable of generating intrinsic gamma oscillations in response to theta input. This gamma generator is independent of activity in the upstream regions, highlighting that CA1 can produce its own gamma oscillation in addition to inheriting activity from the upstream regions. This supports the theory that gamma oscillations predominantly function to achieve local synchrony, and that a local gamma generated in each area conducts the signal to the downstream region.
伽马振荡(30 - 120赫兹)被认为对包括感知和工作记忆在内的各种认知功能很重要,并且这些振荡的破坏与精神分裂症和阿尔茨海默病等脑部疾病有关。海马体的角回区域1(CA1)接收来自上游区域(角回区域3和内侧内嗅皮质)的伽马频率输入,并自身产生更快的伽马振荡。CA1内在伽马振荡的确切性质和起源仍在争论中。在这里,我们在小鼠的CaMKIIα启动子下表达通道视紫红质-2,并制备海马切片以产生内在CA1伽马振荡模型。发现在θ频率下对CA1进行正弦光刺激可诱导出强大的θ嵌套伽马振荡,其时间和空间分布与体内的CA1伽马相似。结果表明在32℃时存在一个频率范围为65 - 75赫兹的单一伽马节律发生器。药理学分析发现这些振荡依赖于AMPA和GABAA受体。细胞贴附和全细胞记录显示,在每个伽马周期内,兴奋性神经元放电略先于中间神经元放电,这表明这种内在的CA1伽马振荡是通过锥体-中间神经元回路机制产生的。
本研究表明角回区域1(CA1)能够响应θ输入产生内在伽马振荡。这个伽马发生器独立于上游区域的活动,突出表明CA1除了从上游区域继承活动外,还能产生自身的伽马振荡。这支持了伽马振荡主要功能是实现局部同步的理论,并且每个区域产生的局部伽马将信号传导至下游区域。