Linking canonical microcircuits and neuronal activity: Dynamic causal modelling of laminar recordings

Neural models describe brain activity at different scales, ranging from single cells to whole brain networks. Here, we attempt to reconcile models operating at the microscopic (compartmental) and mesoscopic (neural mass) scales to analyse data from microelectrode recordings of intralaminar neural activity. Although these two classes of models operate at different scales, it is relatively straightforward to create neural mass models of ensemble activity that are equipped with priors obtained after fitting data generated by detailed microscopic models. This provides generative (forward) models of measured neuronal responses that retain construct validity in relation to compartmental models. We illustrate our approach using cross spectral responses obtained from V1 during a visual perception paradigm that involved optogenetic manipulation of the basal forebrain. We find that the resulting neural mass model can distinguish between activity in distinct cortical layers – both with and without optogenetic activation – and that cholinergic input appears to enhance (disinhibit) superficial layer activity relative to deep layers. This is particularly interesting from the perspective of predictive coding, where neuromodulators are thought to boost prediction errors that ascend the cortical hierarchy

Integral representations of displacements in linear elasticity

AbstractWe present some new formulae for the solution of boundary value problems for a two-dimensional isotropic elastic body. In particular, using the so-called Dbar formalism and the method introduced by Fokas (2008) [4], we obtain integral representations of the Fourier type for the displacements appearing in boundary value problems formulated in an arbitrary convex polygon with n sides

Neural fields, spectral responses and lateral connections

AbstractThis paper describes a neural field model for local (mesoscopic) dynamics on the cortical surface. Our focus is on sparse intrinsic connections that are characteristic of real cortical microcircuits. This sparsity is modelled with radial connectivity functions or kernels with non-central peaks. The ensuing analysis allows one to generate or predict spectral responses to known exogenous input or random fluctuations. Here, we characterise the effect of different connectivity architectures (the range, dispersion and propagation speed of intrinsic or lateral connections) and synaptic gains on spatiotemporal dynamics. Specifically, we look at spectral responses to random fluctuations and examine the ability of synaptic gain and connectivity parameters to induce Turing instabilities. We find that although the spatial deployment and speed of lateral connections can have a profound affect on the behaviour of spatial modes over different scales, only synaptic gain is capable of producing phase-transitions. We discuss the implications of these findings for the use of neural fields as generative models in dynamic causal modeling (DCM)

Moving boundary value problems for the wave equation

AbstractWe study certain boundary value problems for the one-dimensional wave equation posed in a time-dependent domain. The approach we propose is based on a general transform method for solving boundary value problems for integrable nonlinear PDE in two variables, that has been applied extensively to the study of linear parabolic and elliptic equations. Here we analyse the wave equation as a simple illustrative example to discuss the particular features of this method in the context of linear hyperbolic PDEs, which have not been studied before in this framework

Dynamic causal modeling with neural fields

AbstractThe aim of this paper is twofold: first, to introduce a neural field model motivated by a well-known neural mass model; second, to show how one can estimate model parameters pertaining to spatial (anatomical) properties of neuronal sources based on EEG or LFP spectra using Bayesian inference. Specifically, we consider neural field models of cortical activity as generative models in the context of dynamic causal modeling (DCM). This paper considers the simplest case of a single cortical source modeled by the spatiotemporal dynamics of hidden neuronal states on a bounded cortical surface or manifold. We build this model using multiple layers, corresponding to cortical lamina in the real cortical manifold. These layers correspond to the populations considered in classical (Jansen and Rit) neural mass models. This allows us to formulate a neural field model that can be reduced to a neural mass model using appropriate constraints on its spatial parameters. In turn, this enables one to compare and contrast the predicted responses from equivalent neural field and mass models respectively. We pursue this using empirical LFP data from a single electrode to show that the parameters controlling the spatial dynamics of cortical activity can be recovered, using DCM, even in the absence of explicit spatial information in observed data

Anatomical connectivity and the resting state activity of large cortical networks

AbstractThis paper uses mathematical modelling and simulations to explore the dynamics that emerge in large scale cortical networks, with a particular focus on the topological properties of the structural connectivity and its relationship to functional connectivity. We exploit realistic anatomical connectivity matrices (from diffusion spectrum imaging) and investigate their capacity to generate various types of resting state activity. In particular, we study emergent patterns of activity for realistic connectivity configurations together with approximations formulated in terms of neural mass or field models. We find that homogenous connectivity matrices, of the sort of assumed in certain neural field models give rise to damped spatially periodic modes, while more localised modes reflect heterogeneous coupling topologies. When simulating resting state fluctuations under realistic connectivity, we find no evidence for a spectrum of spatially periodic patterns, even when grouping together cortical nodes into communities, using graph theory. We conclude that neural field models with translationally invariant connectivity may be best applied at the mesoscopic scale and that more general models of cortical networks that embed local neural fields, may provide appropriate models of macroscopic cortical dynamics over the whole brain

Statistical decision theory and multiscale analyses of human brain data

Background In the era of Big Data, large scale electrophysiological data from animal and human studies are abundant. These data contain information at multiple spatiotemporal scales. However, current approaches for the analysis of electrophysiological data often contain information at a single spatiotemporal scale only. New method We discuss a multiscale approach for the analysis of electrophysiological data. This is based on combining neural models that describe brain responses at different scales. It allows us to make laminar-specific inferences about neurobiological properties of cortical sources using non invasive human electrophysiology data. Results We provide a mathematical proof of this approach using statistical decision theory. We also consider its extensions to brain imaging studies including data from the same subjects performing different tasks. As an illustration, we show that changes in gamma oscillations between different people might originate from differences in recurrent connection strengths of inhibitory interneurons in layers 5/6. Comparison with existing methods This is a new approach that follows up on our recent work. It is different from other approaches where the scale of spatiotemporal dynamics is fixed. Conclusions We discussed a multiscale approach for the analysis of human MEG data. This uses a neural mass model that includes constraints informed by a compartmental model. This has two advantages. First, it allows us to find differences in cortical laminar dynamics and understand neurobiological properties like neuromodulation, excitation to inhibition balance etc. using non invasive data. Second, it also allows us to validate macroscale models by exploiting animal data