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1.
Cell Rep ; 43(4): 113991, 2024 Apr 23.
Article in English | MEDLINE | ID: mdl-38573855

ABSTRACT

The brain receives constant tactile input, but only a subset guides ongoing behavior. Actions associated with tactile stimuli thus endow them with behavioral relevance. It remains unclear how the relevance of tactile stimuli affects processing in the somatosensory (S1) cortex. We developed a cross-modal selection task in which head-fixed mice switched between responding to tactile stimuli in the presence of visual distractors or to visual stimuli in the presence of tactile distractors using licking movements to the left or right side in different blocks of trials. S1 spiking encoded tactile stimuli, licking actions, and direction of licking in response to tactile but not visual stimuli. Bidirectional optogenetic manipulations showed that sensory-motor activity in S1 guided behavior when touch but not vision was relevant. Our results show that S1 activity and its impact on behavior depend on the actions associated with a tactile stimulus.


Subject(s)
Somatosensory Cortex , Animals , Mice , Somatosensory Cortex/physiology , Male , Touch/physiology , Mice, Inbred C57BL , Optogenetics , Touch Perception/physiology , Behavior, Animal , Female
2.
Cell Rep ; 23(9): 2718-2731.e6, 2018 05 29.
Article in English | MEDLINE | ID: mdl-29847801

ABSTRACT

Sensory perception depends on interactions among cortical areas. These interactions are mediated by canonical patterns of connectivity in which higher areas send feedback projections to lower areas via neurons in superficial and deep layers. Here, we probed the circuit basis of interactions among two areas critical for touch perception in mice, whisker primary (wS1) and secondary (wS2) somatosensory cortices. Neurons in layer 4 of wS2 (S2L4) formed a major feedback pathway to wS1. Feedback from wS2 to wS1 was organized somatotopically. Spikes evoked by whisker deflections occurred nearly as rapidly in wS2 as in wS1, including among putative S2L4 → S1 feedback neurons. Axons from S2L4 → S1 neurons sent stimulus orientation-specific activity to wS1. Optogenetic excitation of S2L4 neurons modulated activity across both wS2 and wS1, while inhibition of S2L4 reduced orientation tuning among wS1 neurons. Thus, a non-canonical feedback circuit, originating in layer 4 of S2, rapidly modulates early tactile processing.


Subject(s)
Feedback, Physiological , Somatosensory Cortex/physiology , Animals , Mice, Inbred C57BL , Neurons/physiology , Orientation , Touch/physiology , Vibrissae/physiology
3.
eNeuro ; 4(3)2017.
Article in English | MEDLINE | ID: mdl-28508035

ABSTRACT

The primary sensory neocortex generates an internal representation of the environment, and its circuit reorganization is thought to lead to a modification of sensory perception. This reorganization occurs primarily through activity-dependent plasticity and has been well documented in animals during early developmental stages. Here, we describe a new method for the noninvasive induction of long-term plasticity in the mature brain: simple transient visual stimuli (i.e., flashing lights) can be used to induce prolonged modifications in visual cortical processing and visually driven behaviors. Our previous studies have shown that, in the primary visual cortex (V1) of mice, a flashing light stimulus evokes a long-delayed response that persists for seconds. When the mice were repetitively presented with drifting grating stimuli (conditioned stimuli) during the flash stimulus-evoked delayed response period, the V1 neurons exhibited a long-lasting decrease in responsiveness to the conditioned stimuli. The flash stimulus-induced underrepresentation of the grating motion was specific to the direction of the conditioned stimuli and was associated with a decrease in the animal's ability to detect the motion of the drifting gratings. The neurophysiological and behavioral plasticity both persisted for at least several hours and required N-methyl-d-aspartate receptor activation in the visual cortex. We propose that flashing light stimuli can be used as an experimental tool to investigate the visual function and plasticity of neuronal representations and perception after a critical period of neocortical plasticity.


Subject(s)
Light , Long-Term Synaptic Depression/physiology , Neurons/physiology , Visual Cortex/physiology , Visual Perception/physiology , Animals , Calcium/metabolism , Evoked Potentials, Visual , Male , Mice, Inbred C57BL , Patch-Clamp Techniques , Periodicity , Photic Stimulation/methods , Receptors, N-Methyl-D-Aspartate/metabolism , Time Factors , Voltage-Sensitive Dye Imaging
4.
Nat Neurosci ; 19(9): 1243-9, 2016 09.
Article in English | MEDLINE | ID: mdl-27437910

ABSTRACT

The brain transforms physical sensory stimuli into meaningful perceptions. In animals making choices about sensory stimuli, neuronal activity in successive cortical stages reflects a progression from sensation to decision. Feedforward and feedback pathways connecting cortical areas are critical for this transformation. However, the computational functions of these pathways are poorly understood because pathway-specific activity has rarely been monitored during a perceptual task. Using cellular-resolution, pathway-specific imaging, we measured neuronal activity across primary (S1) and secondary (S2) somatosensory cortices of mice performing a tactile detection task. S1 encoded the stimulus better than S2, while S2 activity more strongly reflected perceptual choice. S1 neurons projecting to S2 fed forward activity that predicted choice. Activity encoding touch and choice propagated in an S1-S2 loop along feedforward and feedback axons. Our results suggest that sensory inputs converge into a perceptual outcome as feedforward computations are reinforced in a feedback loop.


Subject(s)
Action Potentials/physiology , Choice Behavior/physiology , Somatosensory Cortex/physiology , Touch Perception/physiology , Touch/physiology , Animals , Female , Male , Mice, Inbred C57BL , Mice, Transgenic , Models, Animal , Neurons/physiology
5.
PLoS Biol ; 13(8): e1002231, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26274866

ABSTRACT

Animals are constantly exposed to the time-varying visual world. Because visual perception is modulated by immediately prior visual experience, visual cortical neurons may register recent visual history into a specific form of offline activity and link it to later visual input. To examine how preceding visual inputs interact with upcoming information at the single neuron level, we designed a simple stimulation protocol in which a brief, orientated flashing stimulus was subsequently coupled to visual stimuli with identical or different features. Using in vivo whole-cell patch-clamp recording and functional two-photon calcium imaging from the primary visual cortex (V1) of awake mice, we discovered that a flash of sinusoidal grating per se induces an early, transient activation as well as a long-delayed reactivation in V1 neurons. This late response, which started hundreds of milliseconds after the flash and persisted for approximately 2 s, was also observed in human V1 electroencephalogram. When another drifting grating stimulus arrived during the late response, the V1 neurons exhibited a sublinear, but apparently increased response, especially to the same grating orientation. In behavioral tests of mice and humans, the flashing stimulation enhanced the detection power of the identically orientated visual stimulation only when the second stimulation was presented during the time window of the late response. Therefore, V1 late responses likely provide a neural basis for admixing temporally separated stimuli and extracting identical features in time-varying visual environments.


Subject(s)
Neocortex/physiology , Photic Stimulation , Visual Cortex/physiology , Visual Perception/physiology , Adult , Animals , Electroencephalography , Female , Humans , Male , Mice , Mice, Inbred C57BL , Neurons/physiology , Patch-Clamp Techniques , Photic Stimulation/methods
6.
Cereb Cortex ; 23(2): 293-304, 2013 Feb.
Article in English | MEDLINE | ID: mdl-22314044

ABSTRACT

Cortical synaptic strengths vary substantially from synapse to synapse and exhibit a skewed distribution with a small fraction of synapses generating extremely large depolarizations. Using multiple whole-cell recordings from rat hippocampal CA3 pyramidal cells, we found that the amplitude of unitary excitatory postsynaptic conductances approximates a lognormal distribution and that in the presence of synaptic background noise, the strongest fraction of synapses could trigger action potentials in postsynaptic neurons even with single presynaptic action potentials, a phenomenon termed interpyramid spike transmission (IpST). The IpST probability reached 80%, depending on the network state. To examine how IpST impacts network dynamics, we simulated a recurrent neural network embedded with a few potent synapses. This network, unlike many classical neural networks, exhibited distinctive behaviors resembling cortical network activity in vivo. These behaviors included the following: 1) infrequent ongoing activity, 2) firing rates of individual neurons approximating a lognormal distribution, 3) asynchronous spikes among neurons, 4) net balance between excitation and inhibition, 5) network activity patterns that was robust against external perturbation, 6) responsiveness even to a single spike of a single excitatory neuron, and 7) precise firing sequences. Thus, IpST captures a surprising number of recent experimental findings in vivo. We propose that an unequally biased distribution with a few select strong synapses helps stabilize sparse neuronal activity, thereby reducing the total spiking cost, enhancing the circuit responsiveness, and ensuring reliable information transfer.


Subject(s)
Action Potentials/physiology , CA3 Region, Hippocampal/physiology , Nerve Net/physiology , Synaptic Transmission/physiology , Animals , Excitatory Postsynaptic Potentials/physiology , Female , Male , Patch-Clamp Techniques , Rats , Rats, Wistar
7.
J Physiol Sci ; 61(4): 343-8, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21633910

ABSTRACT

Animals collect sensory information through self-generated movements. Muscle movements drive active feedback of sensory information and determine large parts of the sensory inputs the animal receives; however, little is known about how this active feedback process modulates the ongoing dynamics of the brain. We made electrophysiological recordings from layer 2/3 neurons of the mouse neocortex and compared spontaneous cortical activity in local field potentials and intracellular potential fluctuations between normal and hypomyotonic conditions. We found that pancuronium-induced paralysis did not affect the electrophysiological properties of ongoing cortical activity and its perturbation evoked by visual and tactile stimuli. Thus, internal cortical dynamics are not much affected by active muscle movements, at least, in an acute phase.


Subject(s)
Neocortex/physiology , Paralysis/chemically induced , Paralysis/physiopathology , Action Potentials/drug effects , Action Potentials/physiology , Anesthetics/pharmacology , Animals , Blood Pressure/drug effects , Blood Pressure/physiology , Electrophysiological Phenomena/drug effects , Electrophysiological Phenomena/physiology , Heart Rate/drug effects , Heart Rate/radiation effects , Male , Membrane Potentials/drug effects , Membrane Potentials/physiology , Mice , Mice, Inbred ICR , Neocortex/drug effects , Pancuronium/pharmacology , Patch-Clamp Techniques , Photic Stimulation , Touch/drug effects , Touch/physiology
8.
Neurosci Res ; 64(2): 240-2, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19428706

ABSTRACT

In the slow-wave (SW) state, the vast majority of cortical neurons exhibit mostly synchronized oscillatory activity. In this study, we examined the right-left hemispheric difference in slow-wave timings in urethane-anesthetized mice. We found that interhemispheric cross-correlograms of local field potentials (LFPs) peaked asymmetrically. Double in vivo whole-cell patch-clamp recordings also revealed the interhemispheric temporal disparity of slow wave-relevant synaptic barrages. The data suggest the hemispheric laterality in the slow wave origin.


Subject(s)
Functional Laterality , Neocortex/physiology , Action Potentials , Anesthesia , Animals , Frontal Lobe/physiology , Male , Mice , Neurons/physiology , Occipital Lobe/physiology , Parietal Lobe/physiology , Patch-Clamp Techniques , Sleep Stages/physiology , Synapses/physiology
9.
J Neurophysiol ; 102(1): 636-43, 2009 Jul.
Article in English | MEDLINE | ID: mdl-19386760

ABSTRACT

We introduce a new method to unveil the network connectivity among dozens of neurons in brain slice preparations. While synaptic inputs were whole cell recorded from given postsynaptic neurons, the spatiotemporal firing patterns of presynaptic neuron candidates were monitored en masse with functional multineuron calcium imaging, an optical technique that records action potential-evoked somatic calcium transients with single-cell resolution. By statistically screening the neurons that exhibited calcium transients immediately before the postsynaptic inputs, we identified the presynaptic cells that made synaptic connections onto the patch-clamped neurons. To enhance the detection power, we devised the following points: 1) [K+]e was lowered and [Ca2+]e and [Mg2+]e were elevated, to reduce background synaptic activity and minimize the failure rate of synaptic transmission; and 2) a small fraction of presynaptic neurons was specifically activated by glutamate applied iontophoretically through a glass pipette that was moved to survey the presynaptic network of interest ("trawling"). Then we could theoretically detect 96% of presynaptic neurons activated in the imaged regions with a 1% false-positive error rate. This on-line probing technique would be a promising tool in the study of the wiring topography of neuronal circuits.


Subject(s)
Nerve Net/physiology , Neurons/physiology , Synapses/physiology , Synaptic Transmission/physiology , Animals , Brain Mapping , Calcium/metabolism , Egtazic Acid/analogs & derivatives , Egtazic Acid/metabolism , Glutamic Acid/pharmacology , Hippocampus/cytology , Mice , Mice, Inbred ICR , Models, Neurological , Neurons/drug effects , Optics and Photonics/methods , Organ Culture Techniques , Patch-Clamp Techniques , Rats , Rats, Wistar , Synapses/drug effects , Synaptic Transmission/drug effects , Time Factors
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