The neurotransmitter Acetylcholine (ACh), which plays an essential role in neuroplasticity, sleep and arousal, learning and memory, is also one of the most important neuromodulators in the central nervous system. The hippocampus has long been established to be crucial for memory storage and transformation.The way that ACh interacts with hippocampal neurons and modulates its functionis still elusive.
A recent study published by Prof. Lin Longnian's team might shed light on such interactions. The study was recently published in the field's leading journal, the Journal of Neuroscience (2020-4-29), entitled “The Firing of Theta State-Related Septal Cholinergic Neurons Disrupt Hippocampal Ripple Oscillations via Muscarinic Receptors”.
Prof. Lin's team reported, for the first time, the in vivo electro-physiological characteristics of medial septal (MS) cholinergic neurons, which send the most abundant acetylcholine to the hippocampus. Compared with the simultaneously recorded hippocampal theta oscillations, they found that these two activities are highly correlated with each other.
The in vivo firing rate of one MS cholinergic neuron (blue histogram) coincides with hippocampal theta score (red trace) across different behavior states.
Hippocampal theta oscillations occur during animal active exploration and rapid-eye-movement sleep (REM sleep). They represent an “on-line” learning process closely related to information coding. The highly correlated firing activities of MS cholinergic neurons with hippocampal theta oscillations indicate the potential role of ACh in the process of learning and memory. Can we induce artificial theta oscillation by elevating Ach concentration in the hippocampus and eventually improve memory coding?
Prof. Lin’s team took advantage of combining optogenetic stimulation with multi-channel in vivo recording; they delivered blue light stimulation to the MS to activate cholinergic neurons during slow wave sleep (SWS) when high frequency ripple oscillation (100 – 250 Hz) dominates the local field potential (LFP). Surprisingly, activation of MS cholinergic neurons failed to induce artificial theta oscillations in the hippocampus during SWS. But instead, it completely blocked ripple oscillations.
Optogenetic stimulation of MS cholinergic neurons suppress hippocampal ripple oscillations during SWS.
Hippocampal ripple oscillations are crucial for memory consolidation. Disruption of ripple oscillations during SWS would impair hippocampal-dependent spatial memory. High concentration of Ach in the hippocampus during SWS can also suppress ripple oscillation. How does this process happen? What is the underlying mechanism of such a suppression effect caused by high concentration of Ach?
To answer these questions, Prof. Lin’s team went to pharmacological experiments, looking for answers. The results show that muscarinic M2 and M4 receptors, not M1 and M3 receptors, participated in the cholinergic suppression of hippocampal ripple oscillations caused by optogenetic stimulation to MS cholinergic neurons.
These series of investigations focused on the in vivo firing activities of MS cholinergic neurons and their modulation of hippocampal oscillations. They show that the activity of cholinergic neurons alone was not sufficient to induce hippocampal theta oscillations. One of the important functions of acetylcholine in the hippocampus is to suppress ripples during animal exploration and REM sleep, ensuring theta dominance during such periods.
Illustration of acetylcholine function in the hippocampus – to suppress high frequency ripple oscillations, allowing theta oscillation to dominate.
Prof. Lin and assistant investigator Xu Jiamin are the corresponding authors of this paper. Ma Xiaoyu and Zhang Yiyao, two PhD Students at ECNU are the first authors of this paper. This work was also supported by NYU-ECNU Institute of Brain and Cognitive Science at New York University Shanghai.
The Journal of Neuroscience is a weekly peer-reviewed scientific journal published by the Society for Neuroscience. It covers empirical research on all aspects of neuroscience.
To know more about the study: https://www.jneurosci.org/content/40/18/3591
Source: Shanghai Key Laboratory of Brain Functional Genomics (Ministry of Education) at ECNU,
New York University Shanghai
Copy editor: Philip Nash
Editor: Yu Wenxi