- Poster presentation
- Open Access
Modelling homeostatic control of high-frequency post-synaptic transmission and its effect on metabolic efficiency in the auditory brainstem
BMC Neuroscience volume 14, Article number: P167 (2013)
Intrinsic electrical properties of neurons are controlled by a number of homeostatic mechanisms, among which is the modulation of conductances of voltage-dependent ion channels. One such example is mediated by Nitric Oxide (NO) in principal neurons of the Medial Nucleus of the Trapezoid Body (MNTB) in the auditory brainstem. These act as relay neurons, receiving excitatory input and transmitting inhibitory signals to the auditory nuclei involved in sound localisation. NO is released here in an activity-dependent manner and switches the basis of action potential (AP) repolarisation from Kv3 to Kv2, decreasing intrinsic excitability and improving faithful following of high frequency input trains . We have replicated these effects in a biophysically detailed neuron model and have measured both transmission fidelity and metabolic efficiency of AP generation, quantified by the Na+/K+ charge overlap ratio , across varying states of NO activation.
It is observed that increasing Kv2 conductance leads to improved post-synaptic transmission at high frequencies, while also decreasing the metabolic efficiency of an action potential. The location of Kv2 channels adjacent to Nav channels at the axon initial segment (AIS), as opposed to Kv3, which is located at the soma, is found to be crucial in determining how it affects metabolic efficiency. Figure 1 illustrates that NO mediates transition between a metabolically efficient state sufficient to perform its function at low activity and a metabolically inefficient state required in order to sustain transmission fidelity at high frequencies. This finding provides a plausible justification for the presence of an activity-dependent switch of dominant potassium channel in the MNTB. This effect has subsequently been observed in a CA3 pyramidal cell model , a more generic neuron morphology in which NO is also known to act on Kv conductances .
Steinert JR, Robinson SW, Tong MD, Haustein ID: Nitric oxide is an activity-dependent regulator of target neuron intrinsic excitability. Neuron. 2011, 71 (2): 291-305. 10.1016/j.neuron.2011.05.037.
Hallermann S, de Kock CPJ, Stuart GJ, Kole MHP: State and location dependence of action potential metabolic cost in cortical pyramidal neurons. Nat Neurosci. 2012, 15 (7): 1007-1014. 10.1038/nn.3132.
Traub R, Wong R, Miles R, Michelson H: A model of a CA3 hippocampal pyramidal neuron incorporating voltage-clamp data on intrinsic conductances. J Neurol Neurophysiol. 1991, 66: 635-50.
This work was supported by the Erasmus Mundus EuroSPIN programme (YS) and MRC Fellowship G0900425 (MHH).
About this article
Cite this article
Sweeney, Y., Hellgren-Kotaleski, J. & Hennig, M. Modelling homeostatic control of high-frequency post-synaptic transmission and its effect on metabolic efficiency in the auditory brainstem. BMC Neurosci 14, P167 (2013). https://0-doi-org.brum.beds.ac.uk/10.1186/1471-2202-14-S1-P167
- Nitric Oxide
- Metabolic Efficiency
- Axon Initial Segment
- Relay Neuron
- Intrinsic Excitability