4.7 Article

Species-Specific Adaptation for Ongoing High-Frequency Action Potential Generation in MNTB Neurons

Journal

JOURNAL OF NEUROSCIENCE
Volume 43, Issue 15, Pages 2714-2729

Publisher

SOC NEUROSCIENCE
DOI: 10.1523/JNEUROSCI.2320-22.2023

Keywords

auditory system; comparative neurophysiology; medial nucleus of the trapezoid body; membrane properties; superior olivary complex; synaptic transmission

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Comparative analysis reveals that MNTB neurons in bats and gerbils show similar membrane properties but differ in dendrotoxin-sensitive potassium currents and synaptic properties. The spike generator in bats is able to sustain higher frequency input-output functions and maintain temporal precision compared to gerbils.
Comparative analysis of evolutionarily conserved neuronal circuits between phylogenetically distant mammals highlights the relevant mechanisms and specific adaptations to information processing. The medial nucleus of the trapezoid body (MNTB) is a conserved mammalian auditory brainstem nucleus relevant for temporal processing. While MNTB neurons have been extensively investigated, a comparative analysis of phylogenetically distant mammals and the spike generation is missing. To understand the suprathreshold precision and firing rate, we examined the membrane, voltage-gated ion channel and synaptic properties in Phyllostomus discolor (bat) and in Meriones unguiculatus (rodent) of either sex. Between the two species, the membrane properties of MNTB neurons were similar at rest with only minor differences, while larger dendrotoxin (DTX)-sensitive potassium currents were found in gerbils. Calyx of Held-mediated EPSCs were smaller and frequency dependence of short-term plasticity (STP) less pronounced in bats. Simulating synaptic train stimulations in dynamic clamp revealed that MNTB neurons fired with decreasing success rate near conductance threshold and at increasing stimulation frequency. Driven by STP-dependent conductance decrease, the latency of evoked action potentials increased during train stimulations. The spike generator showed a temporal adaptation at the beginning of train stimulations that can be explained by sodium current inactivation. Compared with gerbils, the spike generator of bats sustained higher frequency input-output functions and upheld the same temporal precision. Our data mechanistically support that MNTB input-output functions in bats are suited to sustain precise high-frequency rates, while for gerbils, temporal precision appears more relevant and an adaptation to high output-rates can be spared.

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