Our results offer a resolution to a central controversy regarding the coupling between neurons, LFP, and BOLD signals by demonstrating, for the first time, that the coupling of single units to the other measures is variable yet it is tightly related to the degree of interneuronal correlations in the human auditory cortex.

Animal studies have shown robust electrophysiological activity in the sensory cortex in the absence of stimuli or tasks. Similarly, recent human functional magnetic resonance imaging (fMRI) revealed widespread, spontaneously emerging cortical fluctuations. However, it is unknown what neuronal dynamics underlie this spontaneous activity in the human brain. Here we studied this issue by combining bilateral single-unit, local field potentials (LFPs) and intracranial electrocorticography (ECoG) recordings in individuals undergoing clinical monitoring. We found slow (<0.1 Hz, following 1/f-like profiles) spontaneous fluctuations of neuronal activity with significant interhemispheric correlations. These fluctuations were evident mainly in neuronal firing rates and in gamma (40-100 Hz) LFP power modulations. Notably, the interhemispheric correlations were enhanced during rapid eye movement and stage 2 sleep. Multiple intracranial ECoG recordings revealed clear selectivity for functional networks in the spontaneous gamma LFP power modulations. Our results point to slow spontaneous modulations in firing rate and gamma LFP as the likely correlates of spontaneous fMRI fluctuations in the human sensory cortex.The neuronal events occurring in the sensory cortex when no stimulus is presented are not well understood. Contrary to traditional feed-forward models of information processing, a growing body of single-unit, LFP, electroencephalography (EEG), and optical imaging data point to robust levels of spontaneous neuronal activity in sensory areas of the mammalian cortex 1-7 . The modulation of such spontaneous neuronal activity can occur on very slow time scales 8, 9 . These robust spontaneous waves pose a challenge for models linking neuronal activity and sensory perception 10,11 , namely in explaining how the brain distinguishes between spontaneous events and vivid sensory percepts. One possibility is that the precise neuronal dynamics differ substantially between spontaneous and sensory-evoked conditions. This

The emergence of memory, a trace of things past, into human consciousness is one of the greatest mysteries of the human mind. Whereas the neuronal basis of recognition memory can be probed experimentally in human and nonhuman primates, the study of free recall requires that the mind declare the occurrence of a recalled memory (an event intrinsic to the organism and invisible to an observer). Here, we report the activity of single neurons in the human hippocampus and surrounding areas when subjects first view cinematic episodes consisting of audiovisual sequences and again later when they freely recall these episodes. A subset of these neurons exhibited selective firing, which often persisted throughout and following specific episodes for as long as 12 seconds. Verbal reports of memories of these specific episodes at the time of free recall were preceded by selective reactivation of the same hippocampal and entorhinal cortex neurons. We suggest that this reactivation is an internally generated neuronal correlate for the subjective experience of spontaneous emergence of human recollection.The human hippocampus and its associated structures in the medial temporal lobe (MTL) transform present experience into future conscious recollections (1-4). Human MTL neurons respond in a highly specific manner to complex stimulus features (5), to complex stimulus categories (5,6), to individual persons or landmarks (7-9), and to previously seen and novel stimuli (5,10,11). These responses have been demonstrated for stationary stimuli and are usually brief, often lasting between 300 and 600 ms following stimulus onset, and rarely persist beyond 1 to 2 s (8). However, the human experience is seldom that of stationary stimuli; rather, we live and operate in a constantly changing environment. In this environment, we encounter complex stimuli constituting episodes, series of variant multimodal representations linked in temporal succession. It is such temporally sequenced information that is processed by the human MTL (12,13) and later becomes available for conscious recollection. For this reason, we set out to examine how neurons in the MTL respond to cinematic sequences depicting

Memory formation requires the placement of experienced events in the same order in which they appeared. A large body of evidence from human studies indicates that structures in the medial temporal lobe are critically involved in forming and maintaining such memories, and complementing evidence from lesion and electrophysiological work in animals support these findings. However, it remains unclear how single cells and networks of cells can signal this temporal relationship between events. Here we used recordings from single cells in the human brain obtained while subjects viewed repeated presentations of cinematic episodes. We found that neuronal activity in successive time segments became gradually correlated, and, as a result, activity in a given time window became a faithful predictor of the activity to follow. This correlation emerged rapidly, within two to three presentations of an episode and exceeded both context-independent and pure stimulus-driven correlations. The correlation was specific for hippocampal neurons, did not occur in the amygdala and anterior cingulate cortex, and was found for single cells, cell pairs, and triplets of cells, supporting the notion that cell assemblies code for the temporal relationships between sensory events. Importantly, this neuronal measure of temporal binding successfully predicted subjects' ability to recall and verbally report the viewed episodes later. Our findings suggest a neuronal substrate for the formation of memory of the temporal order of events. memory formation | temporal binding | medial temporal lobe | single units | electrophysiology M emory formation includes knowledge about temporally dated events and the temporal relations of these events to each other. In human episodic memory, for example, events and concepts are linked together as they appear on the "time arrow," and in the same context in which they appeared (1-4). Many other types of memory (e.g., rote and sequence learning) require the successful encoding of the temporal relationship between events that follow in time. Case studies as well as studies using imaging techniques with human subjects have shown that formation and maintenance of such memories is mediated by different structures in the medial temporal lobe, with the hippocampus playing a major role (1-10). It is now accepted that neurons of the hippocampus are especially bound to reflect associative events, as these neurons sample inputs from a wide range of structures including sensory areas and high-order association cortices involved in recent event processing (2, 3).To study electrophysiological correlates of memory formation, research in the hippocampus of animals has focused on several paradigms that require memory for the temporal order of events (2, 11). These paradigms include learning of associations between pairs of stimuli (12-15), trace conditioning in which the unconditioned stimulus is well separated in time from the conditioned stimulus (16, 17), delayed nonmatch-to-sample (18), sequences of locations in spatial navigati...

An identical sensory stimulus may or may not be incorporated into perceptual experience, depending on the behavioral and cognitive state of the organism. What determines whether a sensory stimulus will be perceived? While different behavioral and cognitive states may share a similar profile of electrophysiology, metabolism, and early sensory responses, neuromodulation is often different and therefore may constitute a key mechanism enabling perceptual awareness. Specifically, noradrenaline improves sensory responses, correlates with orienting toward behaviorally relevant stimuli, and is markedly reduced during sleep, while experience is largely "disconnected" from external events. Despite correlative evidence hinting at a relationship between noradrenaline and perception, causal evidence remains absent. Here, we pharmacologically down- and upregulated noradrenaline signaling in healthy volunteers using clonidine and reboxetine in double-blind placebo-controlled experiments, testing the effects on perceptual abilities and visually evoked electroencephalography (EEG) and fMRI responses. We found that detection sensitivity, discrimination accuracy, and subjective visibility change in accordance with noradrenaline (NE) levels, whereas decision bias (criterion) is not affected. Similarly, noradrenaline increases the consistency of EEG visually evoked potentials, while lower noradrenaline levels delay response components around 200 ms. Furthermore, blood-oxygen-level-dependent (BOLD) fMRI activations in high-order visual cortex selectively vary along with noradrenaline signaling. Taken together, these results point to noradrenaline as a key factor causally linking visual awareness to external world events. VIDEO ABSTRACT.