Analyzing the transient response dynamics of long-term depression in the mouse auditory cortex in vitro through multielectrode-array-based spatiotemporal recordings

Front Neurosci. 2024 Sep 12:18:1448365. doi: 10.3389/fnins.2024.1448365. eCollection 2024.

Abstract

In the auditory cortex, synaptic plasticity, including long-term potentiation (LTP) and long-term depression (LTD), plays crucial roles in information processing and adaptation to the auditory environment. Previous rodent studies have shown lifelong cortical map plasticity, even beyond the critical period of development. While thalamocortical synapses exhibit LTD during the critical period, little is known about LTD in the cortico-cortical connections of the adult mouse auditory cortex. Here, we investigated the transient response dynamics of LTD in layers 2-5 of the mouse auditory cortex following tetanic stimulation (TS) to layer 4. To characterize LTD properties, we developed a recording protocol to monitor activity levels at multiple sites, including those more than 0.45 mm from the TS site. This allowed us to distinguish LTD-induced reductions in neural excitability from other types, including neural activity depletion. Our findings revealed that LTD induced in layer 4 persisted for over 40-min post-TS, indicating robust cortico-cortical LTD. Using electrophysiological data and a modified synaptic model, we identified key receptors involved in synaptic plasticity and their effects on response dynamics, proposing a method for studying LTD in the mature mouse auditory cortex. Particularly, by employing a simple dynamical model, we analyzed and discussed the involvement of key receptors during the transient period of LTD. This study expands our understanding of synaptic plasticity in the mature mouse auditory cortex beyond the critical period, potentially informing future treatments for hearing disorders.

Keywords: auditory cortex; electric stimulation; high-frequency stimulation; local cortical network; long-term depression; multielectrode array; spatiotemporal neural plasticity.

Grants and funding

The author(s) declare that financial support was received for the research, authorship, and/or publication of this article. TT was supported by the Murata Science Foundation, the Suzuken Memorial Foundation, the Nakatani Foundation for Advancement of Measuring Technologies in Biomedical Engineering, a Grant-in-Aid for Exploratory Research [grant number 21 K19755], and a Grant-in-Aid for Scientific Research (B) [grant number 23H03416] (Japan). RF was supported by JSPS Kakenhi [grant number JP23KJ0047].