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1.
Nat Commun ; 15(1): 4782, 2024 Jun 05.
Article in English | MEDLINE | ID: mdl-38839747

ABSTRACT

During perceptually guided decisions, correlates of choice are found as upstream as in the primary sensory areas. However, how well these choice signals align with early sensory representations, a prerequisite for their interpretation as feedforward substrates of perception, remains an open question. We designed a two alternative forced choice task (2AFC) in which male mice compared stimulation frequencies applied to two adjacent vibrissae. The optogenetic silencing of individual columns in the primary somatosensory cortex (wS1) resulted in predicted shifts of psychometric functions, demonstrating that perception depends on focal, early sensory representations. Functional imaging of layer II/III single neurons revealed mixed coding of stimuli, choices and engagement in the task. Neurons with multi-whisker suppression display improved sensory discrimination and had their activity increased during engagement in the task, enhancing selectively representation of the signals relevant to solving the task. From trial to trial, representation of stimuli and choice varied substantially, but mostly orthogonally to each other, suggesting that perceptual variability does not originate from wS1 fluctuations but rather from downstream areas. Together, our results highlight the role of primary sensory areas in forming a reliable sensory substrate that could be used for flexible downstream decision processes.


Subject(s)
Choice Behavior , Optogenetics , Somatosensory Cortex , Vibrissae , Animals , Somatosensory Cortex/physiology , Male , Vibrissae/physiology , Choice Behavior/physiology , Mice , Neurons/physiology , Mice, Inbred C57BL
2.
Front Behav Neurosci ; 14: 159, 2020.
Article in English | MEDLINE | ID: mdl-33088265

ABSTRACT

Pupillometry, the measure of pupil size and reactivity, has been widely used to assess cognitive processes. Changes in pupil size have been shown to correlate with various behavioral states, both externally and internally induced such as locomotion, arousal, cortical state, and decision-making processes. Besides, these pupillary responses have also been linked to the activity of neuromodulatory systems that modulate attention and perception such as the noradrenergic and cholinergic systems. Due to the extent of processes the pupil reflects, we aimed at further resolving pupillary responses in the context of behavioral state and task performance while recording pupillary transients of mice performing a vibrotactile two-alternative forced-choice task (2-AFC). We show that before the presentation of task-relevant information, pre-stimulus, pupil size differentiates between states of disengagement from task performance vs. engagement. Also, when subjects have to attend to task stimuli to attain a reward, post-stimulus, pupillary dilations exhibit a difference between correct and error responses with this difference reflecting an internal decision variable. We hypothesize that this internal decision variable relates to response confidence, the internal perception of the confidence the subject has in its choice. As opposed to this, we show that in a condition of passive performance, when the stimulus has no more task relevance due to reward being provided automatically, pupillary dilations reflect the occurrence of stimulation and reward provision but not decisional variables as under active performance. Our results provide evidence that in addition to reflecting attentiveness under task performance rather than arousal per se, pupil dilations also reflect the confidence of the subject in his ensuing response. This confidence coding is overlaid within a more pronounced pupil dilation that reflects post-decision components that are related to the response itself but not to the decision. We also provide evidence as to how different behavioral states, imposed by task demands, modulate what the pupil is reflecting, presumably showing what the underlying cognitive network is coding for.

3.
J Neural Eng ; 16(6): 066031, 2019 11 06.
Article in English | MEDLINE | ID: mdl-31480027

ABSTRACT

OBJECTIVE: The restoration of vision in blind patients suffering from degenerative retinal diseases like retinitis pigmentosa may be obtained by local electrical stimulation with retinal implants. In this study, a very large electrode array for retinal stimulation (VLARS) was introduced and tested regarding its safety in implantation and biocompatibility. Further, the array's stimulation capabilities were tested in an acute setting. APPROACH: The polyimide-based implants have a diameter of 12 mm, cover approximately 110 mm2 of the retinal surface and carrying 250 iridium oxide coated gold electrodes. The implantation surgery was established in cadaveric porcine eyes. To analyze biocompatibility, ten rabbits were implanted with the VLARS device, and observed for 12 weeks using slit lamp examination, fundus photography, optical coherence tomography (OCT) as well as ultrasound imaging. After enucleation, histological examinations were performed. In acute stimulation experiments, electrodes recorded cortical field potentials upon retinal stimulation in the visual cortex in rabbits. MAIN RESULTS: Implantation studies in rabbits showed that the implantation surgery is safe but difficult. Retinal detachment induced by retinal tears was observed in five animals in varying severity. In five cases, corneal edema reduced the quality of the follow-up examinations. Findings in OCT-imaging and funduscopy suggested that peripheral fixation was insufficient in various animals. Results of the acute stimulation demonstrated the array's ability to elicit cortical responses. SIGNIFICANCE: Overall, it was possible to implant very large epiretinal arrays. On retinal stimulation with the VLARS responses in the visual cortex were recorded. The VLARS device offers the opportunity to restore a much larger field of visual perception when compared to current available retinal implants.


Subject(s)
Biocompatible Materials/administration & dosage , Electrodes, Implanted , Prosthesis Implantation/methods , Retina/physiology , Visual Cortex/physiology , Animals , Follow-Up Studies , Microelectrodes , Prosthesis Implantation/instrumentation , Rabbits , Swine
4.
Cereb Cortex ; 27(1): 863-876, 2017 01 01.
Article in English | MEDLINE | ID: mdl-26628563

ABSTRACT

Stimulus-specific adaptation (SSA) to repetitive stimulation has been proposed to separate behaviorally relevant features from a stream of continuous sensory information. However, the exact mechanisms giving rise to SSA and cortical deviance detection are not well understood. We therefore used an oddball paradigm and multicontact electrodes to characterize single-neuron and local field potential responses to various deviant stimuli across the rat somatosensory cortex. Changing different single-whisker stimulus features evoked robust SSA in individual cortical neurons over a wide range of stimulus repetition rates (0.25-80 Hz). Notably, SSA was weakest in the granular input layer and significantly stronger in the supra- and infragranular layers, suggesting that a major part of SSA is generated within cortex. Moreover, we found a small subset of neurons in the granular layer with a deviant-specific late response, occurring roughly 200 ms after stimulus offset. This late deviant response exhibited true-deviance detection properties that were not explained by depression of sensory inputs. Our results show that deviant responses are actively amplified within cortex and contain an additional late component that is sensitive for context-specific sensory deviations. This strongly implicates deviance detection as a feature of intracortical stimulus processing beyond simple sensory input depression.


Subject(s)
Neurons/physiology , Somatosensory Cortex/physiology , Touch Perception/physiology , Action Potentials , Animals , Electrodes, Implanted , Female , Models, Neurological , Rats, Sprague-Dawley , Vibrissae/physiology
5.
Biomed Opt Express ; 6(11): 4228-37, 2015 Nov 01.
Article in English | MEDLINE | ID: mdl-26600989

ABSTRACT

We present a cost-effective in vivo two-photon microscope with a highly flexible frontend for in vivo research. Our design ensures fast and reproducible access to the area of interest, including rotation of imaging plane, and maximizes space for auxiliary experimental equipment in the vicinity of the animal. Mechanical flexibility is achieved with large motorized linear stages that move the objective in the X, Y, and Z directions up to 130 mm. 360° rotation of the frontend (rotational freedom for one axis) is achieved with the combination of a motorized high precision bearing and gearing. Additionally, the modular design of the frontend, based on commercially available optomechanical parts, allows straightforward updates to future scanning technologies. The design exceeds the mobility of previous movable microscope designs while maintaining high optical performance.

6.
Neuroimage ; 115: 52-63, 2015 Jul 15.
Article in English | MEDLINE | ID: mdl-25934471

ABSTRACT

The rodent whisker system is a preferred model for studying plasticity in the somatosensory cortex (barrel cortex). Contrarily, only a small amount of research has been conducted to characterize the stability of neuronal population activity in the barrel cortex. We used the mouse whisker system to address the neuronal basis of stable perception in the somatosensory cortex. Cortical representation of periodic whisker deflections was studied in populations of neurons in supragranular layers over extended time periods (up to 3 months) with long-term two-photon Ca(2+) imaging in anesthetized mice. We found that in most of the neurons (87%), Ca(2+) responses increased sublinearly with increasing number of contralateral whisker deflections. The imaged population of neurons was activated in a stereotypic way over days and for different deflection rates (pulse frequencies). Thus, pulse frequencies are coded by response strength rather than by distinct neuronal sub-populations. A small population of highly responsive neurons (~3%) was sufficient to decode the whisker stimulus. This conserved functional map, led by a small set of highly responsive neurons, might form the foundation of stable sensory percepts.


Subject(s)
Somatosensory Cortex/physiology , Vibrissae/innervation , Absorptiometry, Photon , Afferent Pathways , Anesthesia , Animals , Electrodes, Implanted , Female , Mice , Mice, Inbred C57BL , Neuroimaging , Neuronal Plasticity/physiology , Physical Stimulation , Sensory Receptor Cells/physiology , Touch/physiology , Touch Perception/physiology , Vibrissae/physiology
7.
Nat Neurosci ; 17(11): 1567-73, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25242306

ABSTRACT

Neocortical responses typically adapt to repeated sensory stimulation, improving sensitivity to stimulus changes, but possibly also imposing limitations on perception. For example, it is unclear whether information about stimulus frequency is perturbed by adaptation or encoded by precise response timing. We addressed this question in rat barrel cortex by comparing performance in behavioral tasks with either whisker stimulation, which causes frequency-dependent adaptation, or optical activation of cortically expressed channelrhodopsin-2, which elicits non-adapting neural responses. Circumventing adaption by optical activation substantially improved cross-hemispheric discrimination of stimulus frequency. This improvement persisted when temporal precision of optically evoked spikes was reduced. We were able to replicate whisker-driven behavior only by applying adaptation rules mimicking sensory-evoked responses to optical stimuli. Conversely, in a change-detection task, animals performed better with whisker than optical stimulation. Our results directly demonstrate that sensory adaptation critically governs the perception of stimulus patterns, decreasing fidelity under steady-state conditions in favor of change detection.


Subject(s)
Adaptation, Physiological/physiology , Behavior, Animal/physiology , Neocortex/physiology , Pattern Recognition, Physiological/physiology , Action Potentials/physiology , Animals , Female , Rats, Sprague-Dawley , Somatosensory Cortex/physiology , Touch/physiology , Vibrissae/physiology
8.
J Neurosci ; 33(35): 14193-204, 2013 Aug 28.
Article in English | MEDLINE | ID: mdl-23986253

ABSTRACT

Vibrissae-related sensorimotor cortex controls whisking movements indirectly via modulation of lower-level sensorimotor loops and a brainstem central pattern generator (CPG). Two different whisker representations in primary motor cortex (vM1) affect whisker movements in different ways. Prolonged microstimulation in RF, a larger anterior subregion of vM1, gives rise to complex face movements and whisker retraction while the same stimulation evokes large-amplitude rhythmic whisker movement in a small caudo-medial area (RW). To characterize the motor cortex representation of explorative whisking movements, here we recorded RW units in head-fixed rats trained to contact a moving object with one whisker. RW single units were found to encode two aspects of whisker movement independently, albeit on slow time scales (hundreds of milliseconds). The first is whisker position. The second consists of speed (absolute velocity), intensity (instantaneous power), and frequency (spectral centroid). The coding for the latter three parameters was tightly correlated and realized by a continuum of RW responses-ranging from a preference of movement to a preference of rest. Information theory analysis indicated that RW spikes carry most information about position and frequency, while intensity and speed are less well represented. Further, investigating multiple and single RW units, we found a lack of phase locking, movement anticipation, and contact-related tactile responses. These findings suggest that RW neither programs detailed whisker trajectories nor initiates them. Nor does it play a role in processing object touch. Its relationship to whisking is thus indirect and may be related to movement monitoring, perhaps using feedback from the CPG.


Subject(s)
Motor Cortex/physiology , Movement , Vibrissae/physiology , Action Potentials , Animals , Central Pattern Generators/physiology , Female , Male , Motor Cortex/cytology , Neurons/physiology , Rats , Rats, Long-Evans , Rats, Sprague-Dawley , Touch , Vibrissae/innervation
9.
J Neurophysiol ; 109(1): 273-84, 2013 Jan.
Article in English | MEDLINE | ID: mdl-23054598

ABSTRACT

Rats and mice receive a constant bilateral stream of tactile information with their large mystacial vibrissae when navigating in their environment. In a two-alternative forced choice paradigm (2-AFC), head-fixed rats and mice learned to discriminate vibrotactile frequencies applied simultaneously to individual whiskers on the left and right sides of the snout. Mice and rats discriminated 90-Hz pulsatile stimuli from pulsatile stimuli with lower repetition frequencies (10-80 Hz) but with identical kinematic properties in each pulse. Psychometric curves displayed an average perceptual threshold of 50.6-Hz and 53.0-Hz frequency difference corresponding to Weber fractions of 0.56 and 0.58 in mice and rats, respectively. Both species performed >400 trials a day (>200 trials per session, 2 sessions/day), with a peak performance of >90% correct responses. In general, rats and mice trained in the identical task showed comparable psychometric curves. Behavioral readouts, such as reaction times, learning rates, trial omissions, and impulsivity, were also very similar in the two species. Furthermore, whisking of the animals before stimulus presentation reduced task performance. This behavioral paradigm, combined with whisker position tracking, allows precise stimulus control in the 2-AFC task for head-fixed rodents. It is compatible with state-of-the-art neurophysiological recording techniques, such as electrophysiology and two-photon imaging, and therefore represents a valuable framework for neurophysiological investigations of perceptual decision-making.


Subject(s)
Choice Behavior/physiology , Conditioning, Operant/physiology , Discrimination, Psychological/physiology , Touch Perception/physiology , Vibrissae/physiology , Animals , Behavior, Animal/physiology , Exploratory Behavior/physiology , Mice , Rats , Somatosensory Cortex/physiology , Touch/physiology
10.
Nat Neurosci ; 15(11): 1539-46, 2012 Nov.
Article in English | MEDLINE | ID: mdl-23086335

ABSTRACT

Sensory maps are reshaped by experience. It is unknown how map plasticity occurs in vivo in functionally diverse neuronal populations because activity of the same cells has not been tracked over long time periods. Here we used repeated two-photon imaging of a genetic calcium indicator to measure whisker-evoked responsiveness of the same layer 2/3 neurons in adult mouse barrel cortex over weeks, first with whiskers intact, then during continued trimming of all but one whisker. Across the baseline period, neurons displayed heterogeneous yet stable responsiveness. During sensory deprivation, responses to trimmed whisker stimulation globally decreased, whereas responses to spared whisker stimulation increased for the least active neurons and decreased for the most active neurons. These findings suggest that recruitment of inactive, 'silent' neurons is part of a convergent redistribution of population activity underlying sensory map plasticity. Sensory-driven responsiveness is a key property controlling experience-dependent activity changes in individual neurons.


Subject(s)
Brain Mapping , Cerebral Cortex/cytology , Neurons/physiology , Sensory Deprivation/physiology , Action Potentials/physiology , Animals , Calcium/metabolism , Computer Simulation , Female , Gene Expression Regulation , Luminescent Proteins/genetics , Luminescent Proteins/metabolism , Male , Mice , Mice, Inbred C57BL , Models, Biological , Neuropil/metabolism , Optics and Photonics , Physical Stimulation , Synapsins/genetics , Synapsins/metabolism , Time Factors , Transduction, Genetic , Vibrissae/innervation
11.
Neuroimage ; 56(2): 601-15, 2011 May 15.
Article in English | MEDLINE | ID: mdl-20406688

ABSTRACT

Conventional decoding methods in neuroscience aim to predict discrete brain states from multivariate correlates of neural activity. This approach faces two important challenges. First, a small number of examples are typically represented by a much larger number of features, making it hard to select the few informative features that allow for accurate predictions. Second, accuracy estimates and information maps often remain descriptive and can be hard to interpret. In this paper, we propose a model-based decoding approach that addresses both challenges from a new angle. Our method involves (i) inverting a dynamic causal model of neurophysiological data in a trial-by-trial fashion; (ii) training and testing a discriminative classifier on a strongly reduced feature space derived from trial-wise estimates of the model parameters; and (iii) reconstructing the separating hyperplane. Since the approach is model-based, it provides a principled dimensionality reduction of the feature space; in addition, if the model is neurobiologically plausible, decoding results may offer a mechanistically meaningful interpretation. The proposed method can be used in conjunction with a variety of modelling approaches and brain data, and supports decoding of either trial or subject labels. Moreover, it can supplement evidence-based approaches for model-based decoding and enable structural model selection in cases where Bayesian model selection cannot be applied. Here, we illustrate its application using dynamic causal modelling (DCM) of electrophysiological recordings in rodents. We demonstrate that the approach achieves significant above-chance performance and, at the same time, allows for a neurobiological interpretation of the results.


Subject(s)
Brain/physiology , Computer Simulation , Models, Neurological , Animals , Rats
12.
Somatosens Mot Res ; 27(4): 131-48, 2010.
Article in English | MEDLINE | ID: mdl-20954892

ABSTRACT

This paper describes experimental techniques with head-fixed, operantly conditioned rodents that allow the control of stimulus presentation and tracking of motor output at hitherto unprecedented levels of spatio-temporal precision. Experimental procedures for the surgery and behavioral training are presented. We place particular emphasis on potential pitfalls using these procedures in order to assist investigators who intend to engage in this type of experiment. We argue that head-fixed rodent models, by allowing the combination of methodologies from molecular manipulations, intracellular electrophysiology, and imaging to behavioral measurements, will be instrumental in combining insights into the functional neuronal organization at different levels of observation. Provided viable behavioral methods are implemented, model systems based on rodents will be complementary to current primate models--the latter providing highest comparability with the human brain, while the former offer hugely advanced methodologies on the lower levels of organization, for example, genetic alterations, intracellular electrophysiology, and imaging.


Subject(s)
Behavior, Animal , Head , Restraint, Physical/instrumentation , Restraint, Physical/methods , Animals , Conditioning, Operant/physiology , Rats , Rats, Long-Evans , Rats, Sprague-Dawley
13.
J Neurosci Methods ; 187(1): 67-72, 2010 Mar 15.
Article in English | MEDLINE | ID: mdl-20036690

ABSTRACT

The present work introduces an electrode microdrive system small enough to be placed into two distinct brain areas in head-fixed mice. To meet the space constraint imposed by the size of mice and the additional presence of a head post, the size and weight of the components were minimized. In the current version, an individual microdrive moves an array of four Reitboeck type electrodes. We report about successful implantation in rats and mice using one or two microdrives. Using two of these devices in individual mice/rats, the recording of parallel single and multi-unit as well as local field potential from prefrontal, motor, somatosensory cortex and hippocampus is demonstrated. The system can be easily constructed with machinery and equipment present in most neurophysiology labs.


Subject(s)
Electronics/instrumentation , Microelectrodes , Action Potentials , Animals , Behavior , Cerebral Cortex/physiology , Electronics/methods , Evoked Potentials , Head/surgery , Hippocampus/physiology , Mice , Mice, Inbred C57BL , Miniaturization , Motor Activity/physiology , Neurons/physiology , Rats , Rats, Long-Evans , Restraint, Physical , Wakefulness
14.
Nat Neurosci ; 13(1): 97-104, 2010 Jan.
Article in English | MEDLINE | ID: mdl-20010824

ABSTRACT

Little is known about the functional role of axotomized cortical neurons that survive spinal cord injury. Large thoracic spinal cord injuries in adult rats result in impairments of hindlimb function. Using retrograde tracers, we found that axotomized corticospinal axons from the hindlimb sensorimotor cortex sprouted in the cervical spinal cord. Mapping of these neurons revealed the emergence of a new forelimb corticospinal projection from the rostral part of the former hindlimb cortex. Voltage-sensitive dye (VSD) imaging and blood-oxygen-level-dependent functional magnetic resonance imaging (BOLD fMRI) revealed a stable expansion of the forelimb sensory map, covering in particular the former hindlimb cortex containing the rewired neurons. Therefore, axotomized hindlimb corticospinal neurons can be incorporated into the sensorimotor circuits of the unaffected forelimb.


Subject(s)
Brain Mapping , Hindlimb/physiopathology , Nerve Regeneration/physiology , Pyramidal Tracts/pathology , Spinal Cord Injuries/pathology , Spinal Cord Injuries/physiopathology , Animals , Axotomy/methods , Behavior, Animal , Cervical Vertebrae , Disease Models, Animal , Female , Fluorescent Dyes , Forelimb/physiopathology , Image Processing, Computer-Assisted/methods , Magnetic Resonance Imaging/methods , Membrane Potentials/physiology , Motor Cortex/blood supply , Motor Cortex/physiopathology , Oxygen/blood , Pyramidal Tracts/blood supply , Pyrazoles , Rats , Rats, Inbred Lew , Statistics, Nonparametric , Thiazoles
15.
J Neurosci ; 29(39): 12210-9, 2009 Sep 30.
Article in English | MEDLINE | ID: mdl-19793979

ABSTRACT

A lateral hemisection injury of the cervical spinal cord results in Brown-Séquard syndrome in humans and rats. The hands/forelimbs on the injured side are rendered permanently impaired, but the legs/hindlimbs recover locomotor functions. This is accompanied by increased use of the forelimb on the uninjured side. Nothing is known about the cortical circuits that correspond to these behavioral adaptations. In this study, on adult rats with cervical spinal cord lateral hemisection lesions (at segment C3/4), we explored the sensory representation and corticospinal projection of the intact (ipsilesional) cortex. Using blood oxygenation level-dependent functional magnetic resonance imaging and voltage-sensitive dye (VSD) imaging, we found that the cortex develops an enhanced representation of the unimpaired forepaw by 12 weeks after injury. VSD imaging also revealed the cortical spatio-temporal dynamics in response to electrical stimulation of the ipsilateral forepaw or hindpaw. Interestingly, stimulation of the ipsilesional hindpaw at 12 weeks showed a distinct activation of the hindlimb area in the intact, ipsilateral cortex, probably via the injury-spared spinothalamic pathway. Anterograde tracing of corticospinal axons from the intact cortex showed sprouting to recross the midline, innervating the spinal segments below the injury in both cervical and lumbar segments. Retrograde tracing of these midline-crossing axons from the cervical spinal cord (at segment C6/7) revealed the formation of a new ipsilateral forelimb representation in the cortex. Our results demonstrate profound reorganizations of the intact sensory-motor cortex after unilateral spinal cord injury. These changes may contribute to the behavioral adaptations, notably for the recovery of the ipsilesional hindlimb.


Subject(s)
Motor Cortex/physiology , Neuronal Plasticity/physiology , Recovery of Function/physiology , Somatosensory Cortex/physiology , Spinal Cord Injuries/physiopathology , Age Factors , Animals , Cervical Vertebrae , Female , Motor Cortex/anatomy & histology , Psychomotor Performance/physiology , Rats , Rats, Inbred Lew , Somatosensory Cortex/anatomy & histology , Spinal Cord Injuries/pathology
16.
Neuroimage ; 48(2): 339-47, 2009 Nov 01.
Article in English | MEDLINE | ID: mdl-19591950

ABSTRACT

Beta+-sensitive probes are useful tools for the measurement of radiotracer kinetics in small animals. They allow the cost-effective development of new PET tracers and offer the possibility to investigate a variety of cerebral processes. The study's main aim was the in vivo evaluation of a probe system for cerebral surface acquisitions. The detector system is a 0.2-mm thick scintillating disk of 3-mm diameter, positioned close to the cerebral surface. The study consists of 4 subparts: (1) simulation of the detection volume, (2) direct comparison with the classic intracortical beta probe regarding its capability to acquire kinetic data, (3) test of the ability to detect local tracer accumulations during infraorbital nerve (ION) electrostimulation and (4) demonstration of the feasibility to measure tracer kinetics in awake animals. Kinetic data acquired with 18F-fluorodeoxyglucose and 15O-H2O were fitted with standard compartment models. The surface probe measurements were in good agreement with those obtained using the intracortical scintillator. ION electrostimulation induced a marked increase in tracer accumulation adequately detected by the surface probe. In the head-fixed animal, a marked change in FDG kinetics was detected between the awake and anesthetized state. The novel surface probe system proved to be a valuable instrument for in vivo radiotracer studies of the cerebral cortex. Its main advantage is the absence of any tissue damage. In addition, serial acquisitions of tracer kinetics in the awake animal turned out to be feasible.


Subject(s)
Cerebral Cortex/diagnostic imaging , Positron-Emission Tomography/instrumentation , Positron-Emission Tomography/methods , Anesthesia , Animals , Calibration , Cerebral Cortex/physiology , Computer Simulation , Electric Stimulation , Equipment Design , Female , Fluorodeoxyglucose F18 , Glucose/metabolism , Kinetics , Models, Neurological , Oxygen Radioisotopes , Rats , Rats, Sprague-Dawley , Somatosensory Cortex/diagnostic imaging , Somatosensory Cortex/physiology , Time Factors , Touch Perception/physiology , Water
17.
J Neurosci ; 28(16): 4283-92, 2008 Apr 16.
Article in English | MEDLINE | ID: mdl-18417708

ABSTRACT

Microglial cells aggregate around amyloid plaques in Alzheimer's disease, but, despite their therapeutic potential, various aspects of their reactive kinetics and role in plaque pathogenesis remain hypothetical. Through use of in vivo imaging and quantitative morphological measures in transgenic mice, we demonstrate that local resident microglia rapidly react to plaque formation by extending processes and subsequently migrating toward plaques, in which individual transformed microglia somata remain spatially stable for weeks. The number of plaque-associated microglia increased at a rate of almost three per plaque per month, independent of plaque volume. Larger plaques were surrounded by larger microglia, and a subset of plaques changed in size over time, with an increase or decrease related to the volume of associated microglia. Far from adopting a more static role, plaque-associated microglia retained rapid process and membrane movement at the plaque/glia interface. Microglia internalized systemically injected amyloid-binding dye at a much higher rate in the vicinity of plaques. These results indicate a role for microglia in plaque maintenance and provide a model with multiple targets for therapeutic intervention.


Subject(s)
Amyloid/metabolism , Microglia/metabolism , Microglia/pathology , Plaque, Amyloid/metabolism , Plaque, Amyloid/pathology , Amyloid/genetics , Animals , Female , Male , Mice , Mice, Inbred C57BL , Mice, Transgenic , Plaque, Amyloid/genetics , Time Factors
18.
Neuron ; 56(5): 907-23, 2007 Dec 06.
Article in English | MEDLINE | ID: mdl-18054865

ABSTRACT

Tactile information is actively acquired and processed in the brain through concerted interactions between movement and sensation. Somatosensory input is often the result of self-generated movement during the active touch of objects, and conversely, sensory information is used to refine motor control. There must therefore be important interactions between sensory and motor pathways, which we chose to investigate in the mouse whisker sensorimotor system. Voltage-sensitive dye was applied to the neocortex of mice to directly image the membrane potential dynamics of sensorimotor cortex with subcolumnar spatial resolution and millisecond temporal precision. Single brief whisker deflections evoked highly distributed depolarizing cortical sensory responses, which began in the primary somatosensory barrel cortex and subsequently excited the whisker motor cortex. The spread of sensory information to motor cortex was dynamically regulated by behavior and correlated with the generation of sensory-evoked whisker movement. Sensory processing in motor cortex may therefore contribute significantly to active tactile sensory perception.


Subject(s)
Behavior, Animal/physiology , Motor Cortex/physiology , Somatosensory Cortex/physiology , Touch/physiology , Animals , Behavior, Animal/drug effects , Fluorescent Dyes , Genetic Vectors , Lentivirus/genetics , Membrane Potentials/physiology , Mice , Motor Cortex/anatomy & histology , Motor Cortex/cytology , Physical Stimulation , Reflex, Monosynaptic/physiology , Somatosensory Cortex/anatomy & histology , Somatosensory Cortex/cytology , Synapses/physiology , Vibrissae/innervation , Vibrissae/physiology
19.
J Neurosci Methods ; 161(1): 118-25, 2007 Mar 30.
Article in English | MEDLINE | ID: mdl-17178423

ABSTRACT

Stimulation mapping of motor cortex is an important tool for assessing motor cortex physiology. Existing techniques include intracortical microstimulation (ICMS) which has high spatial resolution but damages cortical integrity by needle penetrations, and transcranial stimulation which is non-invasive but lacks focality and spatial resolution. A minimally invasive epidural microstimulation (EMS) technique using chronically implanted polyimide-based thin-film microelectrode arrays (72 contacts) was tested in rat motor cortex and compared to ICMS within individual animals. Results demonstrate reliable mapping with high reproducibility and validity with respect to ICMS. No histological evidence of cortical damage and the absence of motor deficits as determined by performance of a motor skill reaching task, demonstrate the safety of the method. EMS is specifically suitable for experiments integrating electrophysiology with behavioral and molecular biology techniques.


Subject(s)
Brain Mapping , Electrodes, Implanted , Microelectrodes , Motor Cortex/physiology , Analysis of Variance , Animals , Behavior, Animal , Electric Stimulation/methods , Electrodes, Implanted/adverse effects , Extremities/innervation , Microelectrodes/adverse effects , Motor Cortex/radiation effects , Rats , Rats, Long-Evans , Reproducibility of Results
20.
Cereb Cortex ; 16(8): 1142-56, 2006 Aug.
Article in English | MEDLINE | ID: mdl-16221924

ABSTRACT

Palpatory movements ('active' touch) are an integral part of tactile sensing. It is known that tactile signals can be modulated in certain behavioral contexts, but it is still unresolved to what degree this modulation is related to movement kinematics and whether it stems from tactile receptors or from central sources. Using awake, head-fixed rats, trained to contact an object, we measured trajectories of muscle-propelled whisker movement precisely and compared tactile responses to contacts thus accomplished with 'passive' contacts (motionless whisker contacted by object). Multielectrode extracellular recordings in deep layers of barrel cortex revealed that when the animals moved their whiskers actively, tactile processing switched from high response amplitudes, wide cortical representation and low background firing, to low response amplitudes, narrow spatial representation and elevated background firing. Switching was fast (<100 ms) and unrelated to the degree of alertness as assessed by spectral analysis of pre-contact field potentials. Switching persisted when information about whisker kinematics was interrupted by transection of the infraorbital nerve and contacts were mimicked by peripheral electrical stimulation. Taken together, these characteristics render central signals derived from the motor system a likely contributor to the processing of active touch.


Subject(s)
Motor Cortex/physiology , Movement/physiology , Nerve Net/physiology , Somatosensory Cortex/physiology , Touch/physiology , Vibrissae/innervation , Vibrissae/physiology , Adaptation, Physiological/physiology , Animals , Female , Male , Rats , Rats, Long-Evans
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