scholarly journals Different inhibitory interneuron cell classes make distinct contributions to visual perception

2018 ◽  
Author(s):  
Jackson J. Cone ◽  
Megan D. Scantlen ◽  
Mark H. Histed ◽  
John H.R. Maunsell
Keyword(s):  
Visual Stimulation ◽  
Inhibitory Neuron ◽  
Inhibitory Interneuron ◽  
Neuron Activity ◽  
Improve Performance ◽  
Sensory Stimuli ◽  
Optogenetic Stimulation ◽  
Visual Contrast ◽  
Cortical Responses ◽  
Contrast Perception

SummaryWhile recent work has revealed how different inhibitory interneurons influence cortical responses to sensory stimuli, little is known about how their activity contributes to sensory perception. Here, we optogenetically stimulated different genetically defined interneurons (parvalbumin (PV), somatostatin (SST), vasoactive intestinal peptide (VIP)) in visual cortex (V1) of mice working at threshold in contrast increment or decrement detection tasks. The visual stimulus was paired with optogenetic stimulation to assess how enhancing V1 inhibitory neuron activity synchronously during cortical responses altered task performance. PV or SST activation impaired, while VIP stimulation improved, contrast increment detection. Notably, PV or SST stimulation also impaired contrast decrement detection, when opsin-evoked inhibition would exaggerate stimulus-evoked decrements in firing rate, and thus might improve performance. The impairment produced by PV or SST stimulation persisted throughout many weeks of testing. In contrast mice learned to reliably detect VIP activation in the absence of natural visual stimulation. Thus, different inhibitory signals make distinct contributions to visual contrast perception.

scholarly journals The impact of bilateral ongoing activity on evoked responses in mouse cortex

eLife ◽  
2019 ◽  
Vol 8 ◽  
Author(s):  
Daisuke Shimaoka ◽  
Nicholas A Steinmetz ◽  
Kenneth D Harris ◽  
Matteo Carandini
Keyword(s):  
Visual Stimulation ◽  
Visual Responses ◽  
Ongoing Activity ◽  
Sensory Stimuli ◽  
Overt Behavior ◽  
Mouse Cortex ◽  
Cortical Responses ◽  
Measured Activity ◽  
External Stimuli ◽  
The Impact

In the absence of external stimuli or overt behavior, the activity of the left and right cortical hemispheres shows fluctuations that are largely bilateral. Here, we show that these fluctuations are largely responsible for the variability observed in cortical responses to sensory stimuli. Using widefield imaging of voltage and calcium signals, we measured activity in the cortex of mice performing a visual detection task. Bilateral fluctuations invested all areas, particularly those closest to the midline. Activity was less bilateral in the monocular region of primary visual cortex and, especially during task engagement, in secondary motor cortex. Ongoing bilateral fluctuations dominated unilateral visual responses, and interacted additively with them, explaining much of the variance in trial-by-trial activity. Even though these fluctuations occurred in regions necessary for the task, they did not affect detection behavior. We conclude that bilateral ongoing activity continues during visual stimulation and has a powerful additive impact on visual responses.

scholarly journals Disinhibitory circuitry gates associative synaptic plasticity in olfactory cortex

2020 ◽  
Author(s):  
Martha Canto-Bustos ◽  
F. Kathryn Friason ◽  
Constanza Bassi ◽  
Anne-Marie M. Oswald
Keyword(s):  
Synaptic Plasticity ◽  
Pyramidal Neurons ◽  
Piriform Cortex ◽  
Inhibitory Neuron ◽  
Long Term Potentiation ◽  
Inhibitory Interneurons ◽  
Sensory Stimuli ◽  
Term Potentiation ◽  
Cortical Responses

AbstractInhibitory microcircuits play an essential role in regulating cortical responses to sensory stimuli. Interneurons that inhibit dendritic or somatic integration in pyramidal neurons act as gatekeepers for neural activity, synaptic plasticity and the formation of sensory representations. Conversely, interneurons that specifically inhibit other interneurons can open gates through disinhibition. In the rodent piriform cortex, relief of dendritic inhibition permits long-term potentiation (LTP) of the recurrent synapses between pyramidal neurons (PNs) thought to underlie ensemble odor representations. We used an optogenetic approach to identify the inhibitory interneurons and disinhibitory circuits that regulate LTP. We focused on three prominent inhibitory neuron classes-somatostatin (SST), parvalbumin (PV), and vasoactive intestinal polypeptide (VIP) interneurons. We find that VIP interneurons inhibit SST interneurons and promote LTP through subthreshold dendritic disinhibition. Alternatively, suppression of PV-interneuron inhibition promotes LTP but requires suprathreshold spike activity. Thus, we have identified two disinhibitory mechanisms to regulate synaptic plasticity during olfactory processing.

scholarly journals Different Inhibitory Interneuron Cell Classes Make Distinct Contributions to Visual Contrast Perception

eNeuro ◽  
2019 ◽  
Vol 6 (1) ◽  
pp. ENEURO.0337-18.2019 ◽  
Author(s):  
Jackson J. Cone ◽  
Megan D. Scantlen ◽  
Mark H. Histed ◽  
John H. R. Maunsell
Keyword(s):  
Inhibitory Interneuron ◽  
Visual Contrast ◽  
Contrast Perception

Comparison of cortical responses to the activation of retina by visual stimulation and transcorneal electrical stimulation

2018 ◽  
Vol 11 (4) ◽  
pp. 667-675 ◽  
Author(s):  
Pengcheng Sun ◽  
Heng Li ◽  
Zhuofan Lu ◽  
Xiaofan Su ◽  
Zengguang Ma ◽  
...  
Keyword(s):  
Electrical Stimulation ◽  
Visual Stimulation ◽  
Transcorneal Electrical Stimulation ◽  
Cortical Responses

scholarly journals Thalamic inputs determine functionally distinct gamma bands in mouse primary visual cortex

2020 ◽  
Author(s):  
Nicolò Meneghetti ◽  
Chiara Cerri ◽  
Elena Tantillo ◽  
Eleonora Vannini ◽  
Matteo Caleo ◽  
...  
Keyword(s):  
Visual Cortex ◽  
Primary Visual Cortex ◽  
Visual Information ◽  
Narrow Band ◽  
Broad Band ◽  
Gamma Band ◽  
Neuron Network ◽  
Sensory Stimuli ◽  
Thalamic Input ◽  
Visual Contrast

AbstractGamma band is known to be involved in the encoding of visual features in the primary visual cortex (V1). Recent results in rodents V1 highlighted the presence, within a broad gamma band (BB) increasing with contrast, of a narrow gamma band (NB) peaking at ∼60 Hz suppressed by contrast and enhanced by luminance. However, the processing of visual information by the two channels still lacks a proper characterization. Here, by combining experimental analysis and modeling, we prove that the two bands are sensitive to specific thalamic inputs associated with complementary contrast ranges. We recorded local field potentials from V1 of awake mice during the presentation of gratings and observed that NB power progressively decreased from low to intermediate levels of contrast. Conversely, BB power was insensitive to low levels of contrast but it progressively increased going from intermediate to high levels of contrast. Moreover, BB response was stronger immediately after contrast reversal, while the opposite held for NB. All the aforementioned dynamics were accurately reproduced by a recurrent excitatory-inhibitory leaky integrate-and-fire network, mimicking layer IV of mouse V1, provided that the sustained and periodic component of the thalamic input were modulated over complementary contrast ranges. These results shed new light on the origin and function of the two V1 gamma bands. In addition, here we propose a simple and effective model of response to visual contrast that might help in reconstructing network dysfunction underlying pathological alterations of visual information processing.Significance StatementGamma band is a ubiquitous hallmark of cortical processing of sensory stimuli. Experimental evidence shows that in the mouse visual cortex two types of gamma activity are differentially modulated by contrast: a narrow band (NB), that seems to be rodent specific, and a standard broad band (BB), observed also in other animal models.We found that narrow band correlates and broad band anticorrelates with visual contrast in two complementary contrast ranges (low and high respectively). Moreover, BB displayed an earlier response than NB. A thalamocortical spiking neuron network model reproduced the aforementioned results, suggesting they might be due to the presence of two complementary but distinct components of the thalamic input into visual cortical circuitry.

scholarly journals Optogenetic spatial and temporal control of cortical circuits on a columnar scale

2016 ◽  
Vol 115 (2) ◽  
pp. 1043-1062 ◽  
Author(s):  
Arani Roy ◽  
Jason J. Osik ◽  
Neil J. Ritter ◽  
Shen Wang ◽  
James T. Shaw ◽  
...  
Keyword(s):  
Visual Stimulation ◽  
Liquid Crystal Display ◽  
Brain Regions ◽  
Cortical Activation ◽  
Mammalian Brain ◽  
Optogenetic Stimulation ◽  
Brain Surface ◽  
Stimulation System ◽  
Circuit Function ◽  
Stimulation Of

Many circuits in the mammalian brain are organized in a topographic or columnar manner. These circuits could be activated—in ways that reveal circuit function or restore function after disease—by an artificial stimulation system that is capable of independently driving local groups of neurons. Here we present a simple custom microscope called ProjectorScope 1 that incorporates off-the-shelf parts and a liquid crystal display (LCD) projector to stimulate surface brain regions that express channelrhodopsin-2 (ChR2). In principle, local optogenetic stimulation of the brain surface with optical projection systems might not produce local activation of a highly interconnected network like the cortex, because of potential stimulation of axons of passage or extended dendritic trees. However, here we demonstrate that the combination of virally mediated ChR2 expression levels and the light intensity of ProjectorScope 1 is capable of producing local spatial activation with a resolution of ∼200–300 μm. We use the system to examine the role of cortical activity in the experience-dependent emergence of motion selectivity in immature ferret visual cortex. We find that optogenetic cortical activation alone—without visual stimulation—is sufficient to produce increases in motion selectivity, suggesting the presence of a sharpening mechanism that does not require precise spatiotemporal activation of the visual system. These results demonstrate that optogenetic stimulation can sculpt the developing brain.

scholarly journals 0071 A Medullary Circuit Controlling REM Sleep

SLEEP ◽  
2020 ◽  
Vol 43 (Supplement_1) ◽  
pp. A29-A29
Author(s):  
A Schott ◽  
J Baik ◽  
S Chung ◽  
F Weber
Keyword(s):  
Rem Sleep ◽  
Theta Rhythm ◽  
National Institutes Of Health ◽  
P Wave ◽  
Neuron Activity ◽  
Brain State ◽  
P Waves ◽  
Optogenetic Stimulation ◽  
Calcium Indicator ◽  
Endogenous Activity

Abstract Introduction Rapid eye movement (REM) sleep is a distinct brain state known for its association with vivid dreaming in humans, though it is also crucial for other mental processes such as memory consolidation and emotion regulation. REM sleep is punctuated by phasic neurophysiological events known as pontine (P)-waves, which are thought to contribute to the cognitive functions of REM sleep. However, little is known about the neural circuits regulating these P-waves, or those responsible for initiating REM sleep itself. Here, we show that a yet unstudied population of medullary neurons expressing corticotropin-releasing-hormone (CRH) are important for controlling both the induction of REM sleep and its phasic events. Methods To measure the endogenous activity of CRH+ neurons in the dorsomedial medulla (dmM), we injected the calcium indicator GCaMP6 in the dmM of CRH-Cre mice. To optogenetically manipulate dmM CRH+ neuron activity, we delivered either an excitatory (ChR2) or inhibitory (iC++) opsin to the dmM of CRH-Cre mice. To record P-waves, we implanted microelectrodes to record local field potentials in the subcoeruleus region of the pons. Results Fiber photometry recordings showed that dmM CRH+ neurons are selectively active during REM sleep, and optogenetic stimulation and inhibition of this population is sufficient to promote and reduce REM sleep, respectively. Additionally, dmM CRH+ neuron activity is correlated with P-waves in the pons, and optogenetic activation of dmM CRH+ cells reliably triggers P-waves during REM sleep. Finally, histological examination of fluorescently labeled dmM CRH+ axons revealed strong projections to several pontine areas involved in P-wave generation as well as modulation of the theta rhythm during REM sleep. Conclusion Our results suggest that dmM CRH+ neurons are involved in controlling REM sleep initiation as well as phasic events within REM sleep. These neurons thus constitute an important component of the brainstem circuitry regulating REM sleep. Support National Institutes of Health (R01 HL149133)

scholarly journals Metabolic tuning of inhibition regulates hippocampal neurogenesis in the adult brain

2020 ◽  
Vol 117 (41) ◽  
pp. 25818-25829
Author(s):  
Xinxing Wang ◽  
Hanxiao Liu ◽  
Johannes Morstein ◽  
Alexander J. E. Novak ◽  
Dirk Trauner ◽  
...  
Keyword(s):  
Dentate Gyrus ◽  
Energy Homeostasis ◽  
Inhibitory Neuron ◽  
Hippocampal Neurogenesis ◽  
Adult Brain ◽  
Adult Hippocampal Neurogenesis ◽  
Neuron Activity ◽  
Adult Mice ◽  
Sphingosine 1 Phosphate ◽  
Underlying Mechanisms

Hippocampus-engaged behaviors stimulate neurogenesis in the adult dentate gyrus by largely unknown means. To explore the underlying mechanisms, we used tetrode recording to analyze neuronal activity in the dentate gyrus of freely moving adult mice during hippocampus-engaged contextual exploration. We found that exploration induced an overall sustained increase in inhibitory neuron activity that was concomitant with decreased excitatory neuron activity. A mathematical model based on energy homeostasis in the dentate gyrus showed that enhanced inhibition and decreased excitation resulted in a similar increase in neurogenesis to that observed experimentally. To mechanistically investigate this sustained inhibitory regulation, we performed metabolomic and lipidomic profiling of the hippocampus during exploration. We found sustainably increased signaling of sphingosine-1-phosphate, a bioactive metabolite, during exploration. Furthermore, we found that sphingosine-1-phosphate signaling through its receptor 2 increased interneuron activity and thus mediated exploration-induced neurogenesis. Taken together, our findings point to a behavior-metabolism circuit pathway through which experience regulates adult hippocampal neurogenesis.

scholarly journals Enhanced Alpha-oscillations in Visual Cortex during Anticipation of Self-generated Visual Stimulation

2014 ◽  
Vol 26 (11) ◽  
pp. 2540-2551 ◽  
Author(s):  
Max-Philipp Stenner ◽  
Markus Bauer ◽  
Patrick Haggard ◽  
Hans-Jochen Heinze ◽  
Ray Dolan
Keyword(s):  
Visual Cortex ◽  
Visual Stimulation ◽  
Sensory Information ◽  
Sensory Stimuli ◽  
Forward Models ◽  
Alpha Oscillations ◽  
Time Frequency ◽  
Sensory Attenuation ◽  
Sensory Neural ◽  
Motor Actions

The perceived intensity of sensory stimuli is reduced when these stimuli are caused by the observer's actions. This phenomenon is traditionally explained by forward models of sensory action–outcome, which arise from motor processing. Although these forward models critically predict anticipatory modulation of sensory neural processing, neurophysiological evidence for anticipatory modulation is sparse and has not been linked to perceptual data showing sensory attenuation. By combining a psychophysical task involving contrast discrimination with source-level time–frequency analysis of MEG data, we demonstrate that the amplitude of alpha-oscillations in visual cortex is enhanced before the onset of a visual stimulus when the identity and onset of the stimulus are controlled by participants' motor actions. Critically, this prestimulus enhancement of alpha-amplitude is paralleled by psychophysical judgments of a reduced contrast for this stimulus. We suggest that alpha-oscillations in visual cortex preceding self-generated visual stimulation are a likely neurophysiological signature of motor-induced sensory anticipation and mediate sensory attenuation. We discuss our results in relation to proposals that attribute generic inhibitory functions to alpha-oscillations in prioritizing and gating sensory information via top–down control.

Activity of precentral neurons during torque-triggered hand movements in awake primates

1979 ◽  
Vol 57 (2) ◽  
pp. 174-184 ◽  
Author(s):  
Y. C. Wong ◽  
H. C. Kwan ◽  
J. T. Murphy
Keyword(s):  
Wrist Joint ◽  
Wrist Flexion ◽  
Somatosensory Stimulation ◽  
Sensory Stimuli ◽  
Neuronal Populations ◽  
Supportive Role ◽  
Flexion Extension ◽  
Cortical Responses ◽  
Early Portion ◽  
Temporally Correlated

In monkeys performing a handle-repositioning task involving primarily wrist flexion–extension (F–E) movements after a torque perturbation was delivered to the handle, single units were recorded extracellularly in the contralateral precentral cortex. Precentral neurons were identified by passive somatosensory stimulation, and were classified into five somatotopically organized populations. Based on electromyographic recordings, it was observed that flexors and extensors about the wrist joint were specifically involved in the repositioning of the handle, while many other muscles which act at the wrist and other forelimb joints were involved in the task in a supportive role. In precentral cortex, all neuronal responses observed were temporally correlated to both the sensory stimuli and the motor responses. Visual stimuli, presented simultaneously with torque perturbations, did not affect the early portion of cortical responses to such torque perturbations. In each of the five somatotopically organized neuronal populations, task-related neurons as well as task-unrelated ones were observed. A significantly larger proportion of wrist (F–E) neurons was related to the task, as compared with the other, nonwrist (F–E) populations. The above findings were discussed in the context of a hypothesis for the function of precentral cortex during voluntary limb movement in awake primates. This hypothesis incorporates a relationship between activities of populations of precentral neurons, defined with respect to their responses to peripheral events at or about single joints, and movements about the same joint.

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