Fear memory contextualization is critical for selecting adaptive behavior to survive. Contextual fear conditioning (CFC) is a classical model for elucidating related underlying neuronal circuits. The primary visual cortex (V1) is the primary cortical region for contextual visual inputs, but its role in CFC is poorly understood. Here, our experiments demonstrated that bilateral inactivation of V1 in mice impaired CFC retrieval, and both CFC learning and extinction increased the turnover rate of axonal boutons in V1. The frequency of neuronal Ca²⁺ activity decreased after CFC learning, while CFC extinction reversed the decrease and raised it to the naïve level. Contrary to control mice, the frequency of neuronal Ca²⁺ activity increased after CFC learning in microglia-depleted mice and was maintained after CFC extinction, indicating that microglial depletion alters CFC learning and the frequency response pattern of extinction-induced Ca²⁺ activity. These findings reveal a critical role of microglia in neocortical information processing in V1, and suggest potential approaches for cellular-based manipulation of acquired fear memory.
Mice ; Animals ; Primary Visual Cortex ; Extinction, Psychological/physiology* ; Learning/physiology* ; Fear/physiology* ; Hippocampus/physiology*

Studies have shown that spatial attention remarkably affects the trial-to-trial response variability shared between neurons. Difficulty in the attentional task adjusts how much concentration we maintain on what is currently important and what is filtered as irrelevant sensory information. However, how task difficulty mediates the interactions between neurons with separated receptive fields (RFs) that are attended to or attended away is still not clear. We examined spike count correlations between single-unit activities recorded simultaneously in the primary visual cortex (V1) while monkeys performed a spatial attention task with two levels of difficulty. Moreover, the RFs of the two neurons recorded were non-overlapping to allow us to study fluctuations in the correlated responses between competing visual inputs when the focus of attention was allocated to the RF of one neuron. While increasing difficulty in the spatial attention task, spike count correlations were either decreased to become negative between neuronal pairs, implying competition among them, with one neuron (or none) exhibiting attentional enhancement of firing rate, or increased to become positive, suggesting inter-neuronal cooperation, with one of the pair showing attentional suppression of spiking responses. Besides, the modulation of spike count correlations by task difficulty was independent of the attended locations. These findings provide evidence that task difficulty affects the functional interactions between different neuronal pools in V1 when selective attention resolves the spatial competition.
Animals ; Attention/physiology* ; Macaca mulatta ; Neurons/physiology* ; Photic Stimulation ; Primary Visual Cortex ; Visual Cortex/physiology*

Crossmodal information processing in sensory cortices has been reported in sparsely distributed neurons under normal conditions and can undergo experience- or activity-induced plasticity. Given the potential role in brain function as indicated by previous reports, crossmodal connectivity in the sensory cortex needs to be further explored. Using perforated whole-cell recording in anesthetized adult rats, we found that almost all neurons recorded in the primary somatosensory, auditory, and visual cortices exhibited significant membrane-potential responses to crossmodal stimulation, as recorded when brain activity states were pharmacologically down-regulated in light anesthesia. These crossmodal cortical responses were excitatory and subthreshold, and further seemed to be relayed primarily by the sensory thalamus, but not the sensory cortex, of the stimulated modality. Our experiments indicate a sensory cortical presence of widespread excitatory crossmodal inputs, which might play roles in brain functions involving crossmodal information processing or plasticity.
Animals ; Auditory Cortex/physiology* ; Neuronal Plasticity/physiology* ; Neurons ; Rats ; Thalamus ; Visual Cortex/physiology*

Visual memory, mainly composed of visual long-term memory (VLTM) and visual working memory (VWM), is an important mechanism of human information storage. Since Baddeley proposed the multicomponent working memory model, the idea that VWM is independent of the VLTM system has been widely accepted. However, the new theoretical evidence suggested a close connection between VLTM and VWM. For instance, the three embedded components model describes the VLTM and VWM in the same framework, which suggests that VWM is only a distinct state of VLTM. On the one hand, the operating function of VWM is supported by the persistence of VLTM. On the other hand, the evidence from neuroimaging studies shows that VWM and VLTM tasks activate some same brain areas. In addition, the whole visual memory system shows a trend of processing from early visual cortex to prefrontal cortex. The present article not only reviews the current studies about the relationship between VLTM and VWM but also gives some forecasts for future studies.
Brain ; physiology ; Humans ; Memory, Long-Term ; Memory, Short-Term ; Visual Cortex ; physiology ; Visual Perception

The core of visual processing is the identification and recognition of the objects relevant to cognitive behaviors. In natural environment, visual input is often comprised of highly complex 3-dimensional signals involving multiple visual objects. One critical determinant of object recognition is visual contour. Despite substantial insights on visual contour processing gained from previous findings, these studies have focused on limited aspects or particular stages of contour processing. So far, a systematic perspective of contour processing that comprehensively incorporates previous evidence is still missing. We therefore propose an integrated framework of the cognitive and neural mechanisms of contour processing, which involves three mutually interacting cognitive stages: contour detection, border ownership assignment and contour integration. For each stage, we provide an elaborated discussion of the neural properties, processing mechanism, and its functional interaction with the other stages by summarizing the relevant electrophysiological and human cognitive neuroscience evidence. Finally, we present the major challenges for further unraveling the mechanisms of visual contour processing.
Cognition ; Form Perception ; Humans ; Visual Cortex ; physiology ; Visual Perception

The human visual system efficiently extracts local elements from cluttered backgrounds and integrates these elements into meaningful contour perception. This process is a critical step before object recognition, in which contours often play an important role in defining the shapes and borders of the to-be-recognized objects. However, the neural mechanism of the contour integration is still under debate. The investigation of the neural mechanism underlying contour integration could deepen our understanding of perceptual grouping in the human visual system and advance the development of the algorithms for image grouping and segmentation in computer vision. Here, we review two theoretical frameworks that were proposed over the past decades. The first framework is based on hardwired horizontal connection in primary visual cortex, while the second one emphasizes the role of recurrent connections within intra- and inter-areas. At the end of review, we also raise the unsolved issues that need to be addressed in future studies.
Form Perception ; Humans ; Models, Neurological ; Pattern Recognition, Visual ; Visual Cortex ; physiology ; Visual Perception

Integrating different visual features into a coherent object is a central challenge for the visual system, which is referred as the binding problem. Firstly, this review introduces the conception of the binding problem and the theoretical and empirical controversies regarding whether and how the binding processes are implemented in visual system. Although many neurons throughout the visual hierarchy are known to code multiple features, feature binding is recruited by visual system. Feature misbinding (or illusory conjunction) is probably the most striking evidence for the existence of the binding mechanism. Next, this review summarizes some critical issues in feature binding literature, including early binding theories, late binding theories, neural synchrony theory, the feature integration theory and re-entry processing theory. Feature binding is not a fully automatic or bottom-up processing. Reentrant connection from higher visual areas to early visual cortex (top-down processes) plays a critical role in feature binding, especially in active feature binding (i.e. feature misbinding). In addition, with electrophysiology, electroencephalography (EEG), magnetoencephalography (MEG) and transcranial electric stimulation (tEs) approaches, recent studies explored both correlational and causal relations between brain oscillations and feature binding, suggesting that brain oscillations are of great importance for feature binding. Finally, this review discusses some potential problems and open questions associated with visual feature binding mechanisms which need to be addressed in future studies.
Brain ; physiology ; Electroencephalography ; Humans ; Magnetoencephalography ; Neurons ; physiology ; Transcranial Direct Current Stimulation ; Visual Cortex ; physiology ; Visual Perception

BACKGROUNDPrevious studies have demonstrated interhemispheric functional connectivity alterations in schizophrenia. However, the relationship between these alterations and the disease state of schizophrenia is largely unknown. Therefore, we aimed to investigate this relationship using voxel-mirrored homotopic connectivity (VMHC) method.

METHODSThis study enrolled 36 schizophrenia patients with complete remission, 58 schizophrenia patients with incomplete remission and 55 healthy controls. The VMHC was calculated based on resting-state functional magnetic resonance imaging data. Differences in VMHC among three groups were compared using one-way analysis of variance. A brain region with a significant difference in VMHC was defined as a region of interest (ROI), and the mean VMHC value in the ROI was extracted for the post hoc analysis, i.e., pair-wise comparisons across the three groups.

RESULTSVMHC in the visual region (inferior occipital and fusiform gyri) and the sensorimotor region (paracentral lobule) showed significant differences among the three groups (P < 0.05, a false discovery rate method corrected). Pair-wise comparisons in the post hoc analysis showed that VMHC of the visual and sensorimotor regions in schizophrenia patients with complete remission and incomplete remission was lower than that in healthy controls (P < 0.05, Bonferroni corrected); however, there was no significant difference between the two patient subgroups.

CONCLUSIONSInterhemispheric functional connectivity in the sensorimotor and visual processing pathways was reduced in patients with schizophrenia, but this reduction was unrelated to the disease state; thus, this reduction may serve as a trait marker of schizophrenia.

Adult ; Brain ; physiology ; Brain Mapping ; Female ; Humans ; Image Processing, Computer-Assisted ; Magnetic Resonance Imaging ; Male ; Schizophrenia ; physiopathology ; Sensorimotor Cortex ; physiology ; Visual Pathways ; physiology

PURPOSE: Blind individuals who have photoreceptor loss are known to perceive phosphenes with electrical stimulation of their remaining retinal ganglion cells. We proposed that implantable lateral geniculate body (LGB) stimulus electrode arrays could be used to generate phosphene vision. We attempted to refine the basic reference of the electrical evoked potentials (EEPs) elicited by microelectrical stimulations of the optic nerve, optic tract and LGB of a domestic pig, and then compared it to visual evoked potentials (VEPs) elicited by short-flash stimuli. METHODS: For visual function measurement, VEPs in response to short-flash stimuli on the left eye of the domestic pig were assessed over the visual cortex at position Oz with the reference electrode at Fz. After anesthesia, linearly configured platinum wire electrodes were inserted into the optic nerve, optic track and LGB. To determine the optimal stimulus current, EEPs were recorded repeatedly with controlling the pulse and power. The threshold of current and charge density to elicit EEPs at 0.3 ms pulse duration was about ±10 microA. RESULTS: Our experimental results showed that visual cortex activity can be effectively evoked by stimulation of the optic nerve, optic tract and LGB using penetrating electrodes. The latency of P1 was more shortened as the electrical stimulation was closer to LGB. The EEPs of two-channel in the visual cortex demonstrated a similar pattern with stimulation of different spots of the stimulating electrodes. We found that the LGB-stimulated EEP pattern was very similar to the simultaneously generated VEP on the control side, although implicit time deferred. CONCLUSIONS: EEPs and VEPs derived from visual-system stimulation were compared. The LGB-stimulated EEP wave demonstrated a similar pattern to the VEP waveform except implicit time, indicating prosthetic-based electrical stimulation of the LGB could be utilized for the blind to perceive vision of phosphenes.
Animals ; Electric Stimulation ; Electrodes, Implanted ; Evoked Potentials, Visual/*physiology ; Geniculate Bodies/*physiology ; Male ; Optic Nerve/physiology ; Optic Tract/physiology ; Photic Stimulation ; Sus scrofa ; Visual Cortex/*physiology

In this research, we compared the visual neuron responses for LGN, A18 and PMLS of old and young cats with extracellular single-neuron recording techniques. We used firing rate vector to characterize information, and response irregularity of cells to evaluate the degeneration of visual characters. Response irregularity is characterized by means of the two coefficients of variation of firing rate vectors: Cv and Cv2. We found that there was no significant change of the response irregularity in LGN areas during the aging process from young to old cats. But in the other two areas, neurons of old cats exhibited significantly larger response irregularity than those of young cats. The result indicated that the information processing function of advanced visual cortex was impaired by aging. This result also provids a reference for the research of the other neuronal system changes during aging process.
Action Potentials ; physiology ; Aging ; physiology ; Animals ; Cats ; Neural Conduction ; Neurons ; physiology ; Visual Cortex ; physiology