Pas de résumé en français / It is generally maintained that one of cortex’ functions is the storage of a large number of memories. In this picture, the physical substrate of memories is thought to be realised in pattern and strengths of synaptic connections among cortical neurons. Memory recall is associated with neuronal activity that is shaped by this connectivity. In this framework, active memories are represented by attractors in the space of neural activity. Electrical activity in cortical neurones in vivo exhibits prominent temporal irregularity. A standard way to account for this phenomenon is to postulate that recurrent synaptic excitation and inhibition as well as external inputs are balanced. In the common view, however, these balanced networks do not easily support the coexistence of multiple attractors. This is problematic in view of memory function. Recently, theoretical studies showed that balanced networks with synapses that exhibit short-term plasticity (STP) are able to maintain multiple stable states. In order to investigate whether experimentally obtained synaptic parameters are consistent with model predictions, we developed a new methodology that is capable to quantify both response variability and STP at the same synapse in an integrated and statistically-principled way. This approach yields higher parameter precision than standard procedures and allows for the use of more efficient stimulation protocols. However, the findings with respect to STP parameters do not allow to make conclusive statements about the validity of synaptic theories of balanced working memory. In the second part of this thesis an alternative theory of cortical memory storage is developed. The theory is based on the assumptions that memories are stored in attractor networks, and that memories are not represented by network states differing in their average activity levels, but by micro-states sharing the same global statistics. Different memories differ with respect to their spatial distributions of firing rates. From this the main result is derived: the balanced state is a necessary condition for extensive memory storage. Furthermore, we analytically calculate memory storage capacities of rate neurone networks. Remarkably, it can be shown that crucial properties of neuronal activity and physiology that are consistent with experimental observations are directly predicted by the theory if optimal memory storage capacity is required.

Die vorliegende Arbeit befasst sich mit dem Einfluss von nicht-weißem oder nicht-Gauß’schem synaptischen Rauschen auf die Informationsübertragung in stochastischen Neuronenmodellen. Ziel ist es, zu verstehen, wie eine Nervenzelle ein Signal in ihrer Pulsaktivität kodiert. Synaptisches Rauschen beschreibt hier den Einfluss anderer Nervenzellen, die nicht das interessierende Signal tragen, aber seine Übertragung durch ihre synaptische Wirkung auf die betrachtete Zelle beeinflussen. In stochastischen Neuronenmodellen wird diese Hintergrundaktivität durch einen stochastischen Prozess mit geeigneter Statistik beschrieben. Ist die Rate, mit der präsynaptische Pulse auftreten, hoch und zeitlich konstant, die Wirkung einzelner Pulse aber verschwindend gering, so wird das synaptische Rauschen durch einen Gauß’schen Prozess beschrieben. Oft wird zudem angenommen, dass das Rauschen unkorreliert (weiß) ist. In dieser Arbeit wird neuronale Signalübertragung in dem Fall untersucht, dass eine solche Näherung nicht mehr gerechtfertigt ist, d.h. wenn der synaptische Hintergrund durch einen stochastischen Prozess beschrieben werden muss, der nicht weiß, nicht Gauß’sch, oder weder weiß noch Gauß’sch ist. Mittels Simulationen und analytischer Rechnungen werden drei Szenarien behandelt: Zunächst betrachten wir eine Zelle, die nicht ein, sondern zwei Signale empfängt, welche zusätzlich durch synaptische Kurzzeitplastizität gefiltert werden. In diesem Fall muss der Hintergrund durch ein farbiges Rauschen beschrieben werden. Im zweiten Szenario betrachten wir den Fall, dass der Effekt einzelner Pulse nicht mehr als schwach angenommen werden kann. Das Rauschen ist dann nicht mehr Gauß’sch, sondern ein Schrotrauschen. Schließlich untersuchen wir den Einfluss einer präsynaptischen Population, deren Feuerrate nicht zeitlich konstant ist, sondern zwischen Phasen hoher und niedriger Aktivität, sogenannten up und down states, springt. In diesem Fall ist das Rauschen weder weiß noch Gauß’sch. / This thesis is concerned with the effect of non-white or non-Gaussian synaptic noise on the information transmission properties of single neurons. Synaptic noise subsumes the massive input that a cell receives from thousands of other neurons. In the framework of stochastic neuron models, this input is described by a stochastic process with suitably chosen statistics. If the overall arrival rate of presynaptic action potentials is high and constant in time and if each individual incoming spike has only a small effect on the dynamics of the cell, the massive synaptic input can be modeled as a Gaussian process. For mathematical tractability, one often assumes that furthermore, the input is devoid of temporal structure, i.e. that it is well described by a Gaussian white noise. This is the so-called diffusion approximation (DA). The present thesis explores neuronal signal transmission when the conditions that underlie the DA are no longer met, i.e. when one must describe the synaptic background activity by a stochastic process that is not white, not Gaussian, or neither. We explore three distinct scenarios by means of simulations and analytical calculations: First, we study a cell that receives not one but two signals, additionally filtered by synaptic short-term plasticity (STP), so that the background has to be described by a colored noise. The second scenario deals with synaptic weights that cannot be considered small; here, the effective noise is no longer Gaussian and the shot-noise nature of the input has to be taken into account. Finally, we study the effect of a presynaptic population that does not fire at a rate which is constant in time but instead undergoes transitions between states of high and low activity, so-called up and down states.