Learning excitatory-inhibitory neuronal assemblies in recurrent networks

Understanding the connectivity observed in the brain and how it emerges from local plasticity rules is a grand challenge in modern neuroscience. In the primary visual cortex (V1) of mice, synapses between excitatory pyramidal neurons and inhibitory parvalbumin-expressing (PV) interneurons tend to be stronger for neurons that respond to similar stimulus features, although these neurons are not topographically arranged according to their stimulus preference. The presence of such excitatory-inhibitory (E/I) neuronal assemblies indicates a stimulus-specific form of feedback inhibition. Here, we show that activity-dependent synaptic plasticity on input and output synapses of PV interneurons generates a circuit structure that is consistent with mouse V1. Computational modeling reveals that both forms of plasticity must act in synergy to form the observed E/I assemblies. Once established, these assemblies produce a stimulus-specific competition between pyramidal neurons. Our model suggests that activity-dependent plasticity can refine inhibitory circuits to actively shape cortical computations.

Acquisition of Abstract Knowledge in Implicit Learning of Anagram Solution Scheme

The article addresses the problem of unconscious gaining of abstract knowledge. Participants solved circular 5-letter anagram arranged by the same invariant scheme. The learned schematic invariant is not perceptive, contrary to the usual invariant acquisition technique in other studies. The possibility of implicit learning of a solution scheme is discussed. Efficiency of anagram solving is compared between the groups with constant or changed solution scheme during the test stage. The change of the solution scheme leads to a decrease of efficiency, i.e. to the lower number of the solved anagrams. The results support the possibility of gaining unconscious abstract knowledge concerning the scheme without any perceptual invariant component. Possible use of a similar stimulus material in studies of interaction between visual and verbal components of working memory is briefly discussed.

Effect of Cross-Orientation Normalization on Different Neural Measures in Macaque Primary Visual Cortex

Divisive normalization is a canonical mechanism that can explain a variety of sensory phenomena. While normalization models have been used to explain spiking activity in response to different stimulus/behavioral conditions in multiple brain areas, it is unclear whether similar models can also explain modulation in population-level neural measures such as power at various frequencies in local field potentials (LFPs) or steady-state visually evoked potential (SSVEP) that is produced by flickering stimuli and popular in electroencephalogram studies. To address this, we manipulated normalization strength by presenting static as well as flickering orthogonal superimposed gratings (plaids) at varying contrasts to 2 female monkeys while recording multiunit activity (MUA) and LFP from the primary visual cortex and quantified the modulation in MUA, gamma (32–80 Hz), high-gamma (104–248 Hz) power, as well as SSVEP. Even under similar stimulus conditions, normalization strength was different for the 4 measures and increased as: spikes, high-gamma, SSVEP, and gamma. However, these results could be explained using a normalization model that was modified for population responses, by varying the tuned normalization parameter and semisaturation constant. Our results show that different neural measures can reflect the effect of stimulus normalization in different ways, which can be modeled by a simple normalization model.

Learning excitatory-inhibitory neuronal assemblies in recurrent networks

In sensory circuits with poor feature topography, stimulus-specific feedback inhibition necessitates carefully tuned synaptic circuitry. Recent experimental data from mouse primary visual cortex (V1) show that synapses between pyramidal neurons and parvalbumin-expressing (PV) inhibitory interneurons tend to be stronger for neurons that respond to similar stimulus features. The mechanism that underlies the formation of such excitatory-inhibitory (E/I) assemblies is unresolved. Here, we show that activity-dependent synaptic plasticity on input and output synapses of PV interneurons generates a circuit structure that is consistent with mouse V1. Using a computational model, we show that both forms of plasticity must act synergistically to form the observed E/I assemblies. Once established, these assemblies produce a stimulus-specific competition between pyramidal neurons. Our model suggests that activity-dependent plasticity can enable inhibitory circuits to actively shape cortical computations.

Evidence of sex differences in the acute impact of oscillatory shear stress on endothelial function

Acutely imposed oscillatory shear stress (OSS) reduces reactive hyperemia flow-mediated dilation (RH-FMD) in conduit arteries of men; however, whether a similar impairment occurs in women or with FMD in response to a controlled, sustained shear stress stimulus (SS-FMD) is unknown. The purpose of this study was to determine the impact of OSS on RH-FMD and SS-FMD in men and women. OSS was provoked in the brachial artery using a 30-min forearm cuff inflation (70 mmHg). Healthy men [ n = 16, 25 yr (SD 3)] and women [ n = 16, 21 yr (SD 2)] completed the OSS intervention twice (separate days). Brachial artery endothelial function was assessed pre- and postintervention via either RH-FMD or 6 min of handgrip SS-FMD using Duplex ultrasound. The RH-FMD stimulus was calculated as shear rate area under the curve 60 s postdeflation (SRAUC60), whereas SS-FMD shear rate was targeted to produce a similar stimulus pre- and postintervention. The OSS intervention decreased RH-FMD in both sexes [men: 6.2% (SD 3.4) to 5.2% (SD 3.0); women: 5.4% (SD 2.0) to 3.1% (SD 1.8), P < 0.001), although this was accompanied by a reduced SRAUC60. There was no significant effect of the intervention on RH-FMD with SRAUC60 as a covariate ( P = 0.310). Handgrip exercise elicited a similar stimulus before and after the intervention ( P = 0.287) in men and women ( P = 0.873). Men demonstrated blunted SS-FMD [4.8% (SD 1.9) to 3.2% (SD 1.9), P < 0.001], whereas women displayed preserved SS-FMD following the intervention [3.5% (SD 1.9) to 4.0% (SD 1.9), P = 0.061]. The lower SS-FMD in men but not women following OSS provides evidence of sex differences in the effects of OSS on conduit artery endothelial function. NEW & NOTEWORTHY Acute exposure to oscillatory shear stress induces transient endothelial dysfunction in men; however, whether women experience similar impairments is unknown. Following acutely imposed oscillatory shear stress, there was a decrease in flow-mediated dilation stimulated by a physiologically relevant sustained increase in shear stress in men but not in premenopausal women. These findings demonstrate, for the first time in humans that there are sex differences in the impact of oscillatory shear stress on endothelial function.

Feature Specific Attention and Return of Fear after Extinction

Anxiety disorders are often treated by repeatedly presenting stimuli that are perceptually similar to original stimuli to which fear was originally acquired. Fear can return after it is extinguished because of the differences between these stimuli. It may possible to attenuate return of fear by manipulating attention to the commonalities between feared stimuli and extinction stimuli. After acquiring fear for an animal-like stimulus by pairing with an electro-cutaneous shock, fear was extinguished by repeatedly presenting a similar stimulus. During extinction participants were asked questions that instructed them to attend towards the features in common between the acquisition and extinction stimulus or towards the unique features of the extinction stimulus. Return of fear was assessed by presenting a second perceptually similar stimulus after extinction. Participants showed a return in skin conductance responding after extinction in the unique condition, and not in the common condition. Both groups showed a return in self-report ratings of US expectancy. Neither group showed a return in fear potentiated startle, but there was evidence that this may have been due to individual differences in emotional attentional control. Our conclusions are limited by the use of a self-report measure of emotional attentional control and the absence of limits on the length of time participants could take to answer the extinction questions. It may be possible to enhance extinction and prevent a return of the physiological aspects of fear by manipulating attention during extinction. However, this does not appear to influence explicit expectancy of aversive outcomes. Individual differences in attentional control may influence this process.

Oculomotor activity parameters of the operator in the P300 brain computer interface and similar stimulus situations

Hypotheses about the relationship of the processes of visual perception and variations of the task in an identical stimulus environment was tested. The following tasks were tested: 1) a simple observation of the illuminations of the character in the matrix; 2) counting the number of highlights; 3) monitoring of the target symbol highlights and typing text with the P300 BCI. In a group of 14 people showed that the highest average length of visual fixation and the lowest dispersion of fixation observed for the second type of task. Statistically significant differences in the level of dispersion of visual fixations found between 1-2 and 1-3 modes; differences between the modes for the duration of fixations are at trends. Significant differences in the number of visual fixations on the target symbols wasn’t detected. The overall conclusion is the high perspective of pairing methodology brain-computer interface on the P300 wave with eye tracking to optimize the characteristics of the stimulus in the BCI environment. The differences in the parameters of oculomotor activity between the tasks reflect the level of attention concentration in the target symbols of the P300 BCI