The deep cerebellar nuclei (DCN) function as output gates for a large majority of the Purkinje cells of the cerebellar cortex and thereby determine how the cerebellum influences the rest of the brain and body. In my PhD programme I have investigated how the DCN process two kinds of input patterns received from Purkinje cells: irregularity of spike intervals and pauses in Purkinje cell activity resulting from the recognition of patterns received at the synapses with the upstream parallel fibres (PFs). To that objective I have created a network system of biophysically realistic Purkinje cell and DCN neuron models that enables the exploration of a wide range of network structure and cell physiology parameters. With this system I have performed simulations that show how the DCN neuron changes the information modality of its input, consisting of varying regularity in Purkinje cell spike intervals, to varying spike rates in its output to the nervous system outside of the cerebellum. This was confirmed in simulations where I exchanged the artificial Purkinje cell trains for those received from experimental collaborators. In pattern recognition simulations I have found that the morphological arrangement present in the cerebellum, where multiple Purkinje cells connect to each DCN neuron, has the effect of amplifying pattern recognition already performed in the Purkinje cells. Using the metric of signal-to-noise ratio I show that PF patterns previously encountered and stored in PF - Purkinje cell synapses are most clearly distinguished from those novel to the system by a 10-20 ms shortened burst firing of the DCN neuron. This result suggests that the effect on downstream targets of these excitatory projection neurons is a decreased excitation when a stored as opposed to novel pattern is received. My work has contributed to a better understanding of information processing in the cerebellum, with implications for human motor control as well as the increasingly recognised non-motor functions of the cerebellum.

This (cumulative) dissertation is concerned with mechanisms and models of information processing and transmission by individual neurons and small neural assemblies. In this document, I first provide historical context for these ideas and highlight similarities and differences to related concepts from machine learning and neuromorphic engineering. With this background, I then discuss the four main themes of my work, namely dendritic filtering and delays, homeostatic plasticity and adaptation, rate-coding with spiking neurons, and spike-timing based alternatives to rate-coding. The content of this discussion is in large part derived from several of my own publications included in Appendix C, but it has been extended and revised to provide a more accessible and broad explanation of the main ideas, as well as to show their inherent connections. I conclude that fundamental differences remain between our understanding of information processing and transmission in machine learning on the one hand and theoretical neuroscience on the other, which should provide a strong incentive for further interdisciplinary work on the domain boundaries between neuroscience, machine learning and neuromorphic engineering.