Human Verbal Memory Encoding Is Hierarchically Distributed in a Continuous Processing Stream.

Processing of memory is supported by coordinated activity in a network of sensory, association, and motor brain regions. It remains a major challenge to determine where memory is encoded for later retrieval. Here, we used direct intracranial brain recordings from epilepsy patients performing free recall tasks to determine the temporal pattern and anatomical distribution of verbal memory encoding across the entire human cortex. High γ frequency activity (65-115 Hz) showed consistent power responses during encoding of subsequently recalled and forgotten words on a subset of electrodes localized in 16 distinct cortical areas activated in the tasks. More of the high γ power during word encoding, and less power before and after the word presentation, was characteristic of successful recall and observed across multiple brain regions. Latencies of the induced power changes and this subsequent memory effect (SME) between the recalled and forgotten words followed an anatomical sequence from visual to prefrontal cortical areas. Finally, the magnitude of the memory effect was unexpectedly found to be the largest in selected brain regions both at the top and at the bottom of the processing stream. These included the language processing areas of the prefrontal cortex and the early visual areas at the junction of the occipital and temporal lobes. Our results provide evidence for distributed encoding of verbal memory organized along a hierarchical posterior-to-anterior processing stream

Network Approaches to Understand Individual Differences in Brain Connectivity: Opportunities for Personality Neuroscience

Over the past decade, advances in the interdisciplinary field of network science have provided a framework for understanding the intrinsic structure and function of human brain networks. A particularly fruitful area of this work has focused on patterns of functional connectivity derived from noninvasive neuroimaging techniques such as functional magnetic resonance imaging (fMRI). An important subset of these efforts has bridged the computational approaches of network science with the rich empirical data and biological hypotheses of neuroscience, and this research has begun to identify features of brain networks that explain individual differences in social, emotional, and cognitive functioning. The most common approach estimates connections assuming a single configuration of edges that is stable across the experimental session. In the literature, this is referred to as a static network approach, and researchers measure static brain networks while a subject is either at rest or performing a cognitively demanding task. Research on social and emotional functioning has primarily focused on linking static brain networks with individual differences, but recent advances have extended this work to examine temporal fluctuations in dynamic brain networks. Mounting evidence suggests that both the strength and flexibility of time-evolving brain networks influence individual differences in executive function, attention, working memory, and learning. In this review, we first examine the current evidence for brain networks involved in cognitive functioning. Then we review some preliminary evidence linking static network properties to individual differences in social and emotional functioning. We then discuss the applicability of emerging dynamic network methods for examining individual differences in social and emotional functioning. We close with an outline of important frontiers at the intersection between network science and neuroscience that will enhance our understanding of the neurobiological underpinnings of social behavior

The Neural Correlates of Visual Hallucinations in Parkinson's Disease

Visual hallucinations are common in Parkinson’s disease (PD) and linked to worse outcomes: increased mortality, higher carer burden, cognitive decline, and worse quality of life. Recent functional studies have aided our understanding, showing large-scale brain network imbalance in PD hallucinations. Imbalance of different influences on visual perception also occurs, with impaired accumulation of feedforward signals from the eyes and visual parts of the brain. Whether feedback signals from higher brain control centres are also affected is unknown and the mechanisms driving network imbalance in PD hallucinations remain unclear. In this thesis I will clarify the computational and structural changes underlying PD hallucinations and link these to functional abnormalities and regional changes at the cellular level. To achieve this, I will employ behavioural testing, diffusion weighted imaging, structural and functional MRI in PD patients with and without hallucinations. I will quantify the use of prior knowledge during a visual learning task and show that PD with hallucinations over-rely on feedback signals. I will examine underlying structural connectivity changes at baseline and longitudinally and will show that posterior thalamic connections are affected early, with frontal connections remaining relatively preserved. I will show that PD hallucinations are associated with a subnetwork of reduced structural connectivity strength, affecting areas crucial for switching the brain between functional states. I will assess the role of the thalamus as a potential driver of network-level changes and show preferential medial thalamus involvement. I will utilise data from the Allen Institute transcription atlas and show how differences in regional gene expression in health contributes to the selective vulnerability of specific white matter connections in PD hallucinations. These findings reveal the structural correlates of visual hallucinations in PD, link these to functional and behavioural changes and provide insights into the cellular mechanisms that drive regional vulnerability, ultimately leading to hallucinations