Correlated variability and its attentional modulation depend on anatomical connectivity.

Visual cortical neurons show variability in their responses to repeated presentations of a stimulus and a portion of this variability is shared across neurons. Attention may enhance visual perception by reducing shared spiking variability. However, shared variability and its attentional modulation are not consistent within or across cortical areas, and depend on additional factors such as neuronal type.

Attention differentially modulates multiunit activity in the lateral geniculate nucleus and V1 of macaque monkeys.

Attention promotes the selection of behaviorally relevant sensory signals from the barrage of sensory information available. Visual attention modulates the gain of neuronal activity in all visual brain areas examined, although magnitudes of gain modulations vary across areas. For example, attention gain magnitudes in the dorsal lateral geniculate nucleus (LGN) and primary visual cortex (V1) vary tremendously across fMRI measurements in humans and electrophysiological recordings in behaving monkeys.

Changes in Local Network Activity Approximated by Reverse Spike-Triggered Local Field Potentials Predict the Focus of Attention.

The effects of visual spatial attention on neuronal firing rates have been well characterized for neurons throughout the visual processing hierarchy. Interestingly, the mechanisms by which attention generates more or fewer spikes in response to a visual stimulus remain unknown. One possibility is that attention boosts the likelihood that synaptic inputs to a neuron result in spikes.

Attention Enhances the Efficacy of Communication in V1 Local Circuits.

Attention is a critical component of visual perception; however, the mechanisms of attention at the granular level are poorly understood. One possible mechanism by which attention modulates neuronal activity is to control the efficacy of communication between connected neurons; however, it is unclear whether attention alters communication efficacy across a variety of neuronal circuits. In parallel, attentional modulation of neuronal firing rate is not uniform but depends upon the match between neuronal feature selectivity and the feature required for successful task completion.

Phase shifts in high-beta- and low-gamma-band local field potentials predict the focus of visual spatial attention.

The local field potential (LFP) contains rich information about activity in local neuronal populations. However, it has been challenging to establish direct links between LFP modulations and task-relevant behavior or cognitive processes, such as attention. We sought to determine whether LFP amplitude or phase modulations are predictive of the allocation of visual spatial attention.

Dynamic communication of attention signals between the LGN and V1.

Correlations and inferred causal interactions among local field potentials (LFPs) simultaneously recorded in distinct visual brain areas can provide insight into how visual and cognitive signals are communicated between neuronal populations. Based on the known anatomical connectivity of hierarchically organized visual cortical areas and electrophysiological measurements of LFP interactions, a framework for interareal frequency-specific communication has emerged. Our goals were to test the predictions of this framework in the context of the early visual pathways and to understand how attention modulates communication between the visual thalamus and primary visual cortex.

Attentional Modulation of Neuronal Activity Depends on Neuronal Feature Selectivity.

Attention exerts a powerful influence on visual perception. The impact of attention on neuronal activity manifests at early visual information processing stages and progressively increases throughout the visual cortical hierarchy. However, the neuronal mechanisms of attention are unresolved.

Cloning and expression of a zebrafish 5-HT(2C) receptor gene.

The 5-HT(2C) receptor is one of 14 different serotonin (5-HT) receptors that control neural function and behavior. Here, we present the entire sequence of a zebrafish 5-HT(2C) receptor cDNA including the 3' untranslated region and the previously unknown 5' untranslated region. The cloned 5-HT(2C) receptor gene is located on chromosome 7, is approximately 202 kbp long, and contains six exons.