Interchangeable Role of Motor Cortex and Reafference for the Stable Execution of an Orofacial Action

Animals interact with their environment through mechanically active, mobile sensors. The efficient use of these sensory organs implies the ability to track their position; otherwise, perceptual stability or prehension would be profoundly impeded. The nervous system may keep track of the position of a sensorimotor organ via two complementary feedback mechanisms—peripheral reafference (external, sensory feedback) and efference copy (internal feedback). Yet, the potential contributions of these mechanisms remain largely unexplored. By training male rats to place one of their vibrissae within a predetermined angular range without contact, a task that depends on knowledge of vibrissa position relative to their face, we found that peripheral reafference is not required. The presence of motor cortex is not required either, except in the absence of peripheral reafference to maintain motor stability. Finally, the red nucleus, which receives descending inputs from motor cortex and cerebellum and projects to facial motoneurons, is critically involved in the execution of the vibrissa positioning task. All told, our results point toward the existence of an internal model that requires either peripheral reafference or motor cortex to optimally drive voluntary motion. SIGNIFICANCE STATEMENT How does an animal know where a mechanically active, mobile sensor lies relative to its body? We address this basic question in sensorimotor integration using the motion of the vibrissae in rats. We show that rats can learn to reliably position their vibrissae in the absence of sensory feedback or in the absence of motor cortex. Yet, when both sensory feedback and motor cortex are absent, motor precision is degraded. This suggests the existence of an internal model able to operate in closed- and open-loop modes, requiring either motor cortex or sensory feedback to maintain motor stability.

[1]  D. Kleinfeld,et al.  The whisking oscillator circuit , 2022, Nature.

[2]  D. Yanagihara,et al.  A Model of Predictive Postural Control Against Floor Tilting in Rats , 2021, Frontiers in Systems Neuroscience.

[3]  D. Kleinfeld,et al.  A vibrissa pathway that activates the limbic system , 2021, bioRxiv.

[4]  Eiman Azim,et al.  Modulation of tactile feedback for the execution of dexterous movement , 2021, bioRxiv.

[5]  D. Feldman,et al.  Cortical Coding of Whisking Phase during Surface Whisking , 2020, Current Biology.

[6]  Samuel Andrew Hires,et al.  The Sensorimotor Basis of Whisker-Guided Anteroposterior Object Localization in Head-Fixed Mice , 2019, Current Biology.

[7]  Elisabeth A. Murray,et al.  Lesion Studies in Contemporary Neuroscience , 2019, Trends in Cognitive Sciences.

[8]  Daniel M Wolpert,et al.  Internal Models in Biological Control , 2019, Annu. Rev. Control. Robotics Auton. Syst..

[9]  D. Angelaki,et al.  Genetically eliminating Purkinje neuron GABAergic neurotransmission increases their response gain to vestibular motion , 2019, Proceedings of the National Academy of Sciences.

[10]  Rodrigo S. Maeda,et al.  Feedforward and Feedback Control Share an Internal Model of the Arm's Dynamics , 2018, The Journal of Neuroscience.

[11]  Mark T. Harnett,et al.  Active dendritic integration and mixed neocortical network representations during an adaptive sensing behavior , 2018, Nature Neuroscience.

[12]  Robert H Wurtz,et al.  Corollary Discharge Contributions to Perceptual Continuity Across Saccades. , 2018, Annual review of vision science.

[13]  Kyle S Severson,et al.  Coding of whisker motion across the mouse face , 2019, eLife.

[14]  Danique Jeurissen,et al.  Focal optogenetic suppression in macaque area MT biases direction discrimination and decision confidence, but only transiently , 2018, eLife.

[15]  Bence P Ölveczky,et al.  The promise and perils of causal circuit manipulations , 2018, Current Opinion in Neurobiology.

[16]  M. Farrell,et al.  The DREADD agonist clozapine N-oxide (CNO) is reverse-metabolized to clozapine and produces clozapine-like interoceptive stimulus effects in rats and mice , 2018, Scientific Reports.

[17]  Fan Wang,et al.  Circuits in the Rodent Brainstem that Control Whisking in Concert with Other Orofacial Motor Actions , 2018, Neuroscience.

[18]  Brandon K. Harvey,et al.  Chemogenetics revealed: DREADD occupancy and activation via converted clozapine , 2017, Science.

[19]  Jianing Yu,et al.  Mechanisms underlying a thalamocortical transformation during active tactile sensation , 2017, PLoS Comput. Biol..

[20]  Kyle S Severson,et al.  Active Touch and Self-Motion Encoding by Merkel Cell-Associated Afferents , 2017, Neuron.

[21]  C. Petersen,et al.  Movement Initiation Signals in Mouse Whisker Motor Cortex , 2016, Neuron.

[22]  Michael Brecht,et al.  Vibrissa motor cortex activity suppresses contralateral whisking behavior , 2016, Nature Neuroscience.

[23]  D. Kleinfeld,et al.  Circuits in the Ventral Medulla That Phase-Lock Motoneurons for Coordinated Sniffing and Whisking , 2016, Neural plasticity.

[24]  J. Izawa,et al.  The cerebro-cerebellum: Could it be loci of forward models? , 2016, Neuroscience Research.

[25]  George J Augustine,et al.  The cerebellum linearly encodes whisker position during voluntary movement , 2016, eLife.

[26]  E. Ahissar,et al.  On-going computation of whisking phase by mechanoreceptors , 2016, Nature Neuroscience.

[27]  Juliana Y. Rhee,et al.  Acute off-target effects of neural circuit manipulations , 2015, Nature.

[28]  Jean-Christophe Comte,et al.  Whisking-Related Changes in Neuronal Firing and Membrane Potential Dynamics in the Somatosensory Thalamus of Awake Mice. , 2015, Cell reports.

[29]  D. Kleinfeld,et al.  Vibrissa Self-Motion and Touch Are Reliably Encoded along the Same Somatosensory Pathway from Brainstem through Thalamus , 2015, PLoS biology.

[30]  Amy J Bastian,et al.  Cerebellar damage impairs internal predictions for sensory and motor function , 2015, Current Opinion in Neurobiology.

[31]  David Kleinfeld,et al.  Juxtacellular Monitoring and Localization of Single Neurons within Sub-cortical Brain Structures of Alert, Head-restrained Rats. , 2015, Journal of visualized experiments : JoVE.

[32]  Anthony Leonardo,et al.  Internal models direct dragonfly interception steering , 2014, Nature.

[33]  Varun Sreenivasan,et al.  Parallel pathways from motor and somatosensory cortex for controlling whisker movements in mice , 2014, The European journal of neuroscience.

[34]  Bryan L. Roth,et al.  Silencing Synapses with DREADDs , 2014, Neuron.

[35]  L. Abbott,et al.  Presynaptic inhibition of spinal sensory feedback ensures smooth movement , 2014, Nature.

[36]  David Kleinfeld,et al.  Spectral methods for functional brain imaging. , 2014, Cold Spring Harbor protocols.

[37]  Zengcai V. Guo,et al.  Flow of Cortical Activity Underlying a Tactile Decision in Mice , 2014, Neuron.

[38]  B. Alstermark,et al.  The lateral reticular nucleus: a precerebellar centre providing the cerebellum with overview and integration of motor functions at systems level. A new hypothesis , 2013, The Journal of physiology.

[39]  David Kleinfeld,et al.  Hierarchy of orofacial rhythms revealed through whisking and breathing , 2013, Nature.

[40]  Xiang Zhou,et al.  New Modules Are Added to Vibrissal Premotor Circuitry with the Emergence of Exploratory Whisking , 2013, Neuron.

[41]  J. Delgado-García,et al.  Red Nucleus Neurons Actively Contribute to the Acquisition of Classically Conditioned Eyelid Responses in Rabbits , 2012, The Journal of Neuroscience.

[42]  Lin Tian,et al.  Activity in motor-sensory projections reveals distributed coding in somatosensation , 2012, Nature.

[43]  T. Hadlock,et al.  The convergence of facial nerve branches providing whisker pad motor supply in rats: Implications for facial reanimation study , 2012, Muscle & nerve.

[44]  A. Keller,et al.  Vibrissae motor cortex unit activity during whisking. , 2012, Journal of neurophysiology.

[45]  D. Kleinfeld,et al.  Neuronal Basis for Object Location in the Vibrissa Scanning Sensorimotor System , 2011, Neuron.

[46]  Daniel N. Hill,et al.  Primary Motor Cortex Reports Efferent Control of Vibrissa Motion on Multiple Timescales , 2011, Neuron.

[47]  Karel Svoboda,et al.  Long-Range Neuronal Circuits Underlying the Interaction between Sensory and Motor Cortex , 2011, Neuron.

[48]  Nathan G. Clack,et al.  Vibrissa-Based Object Localization in Head-Fixed Mice , 2010, The Journal of Neuroscience.

[49]  Christophe Bourdin,et al.  Force-field adaptation without proprioception: Can vision be used to model limb dynamics? , 2010, Neuropsychologia.

[50]  Bijan Pesaran,et al.  Chronux: a platform for analyzing neural signals , 2009, BMC Neuroscience.

[51]  D. Kleinfeld,et al.  Phase-to-rate transformations encode touch in cortical neurons of a scanning sensorimotor system , 2009, Nature Neuroscience.

[52]  M. Sommer,et al.  Corollary discharge across the animal kingdom , 2008, Nature Reviews Neuroscience.

[53]  Michael Brecht,et al.  Whisker movements evoked by stimulation of single motor neurons in the facial nucleus of the rat. , 2008, Journal of neurophysiology.

[54]  J. Krakauer,et al.  A computational neuroanatomy for motor control , 2008, Experimental Brain Research.

[55]  D. Kleinfeld,et al.  Active Spatial Perception in the Vibrissa Scanning Sensorimotor System , 2007, PLoS biology.

[56]  Per Magne Knutsen,et al.  Haptic Object Localization in the Vibrissal System: Behavior and Performance , 2006, The Journal of Neuroscience.

[57]  J. Vercher,et al.  Internally driven control of reaching movements: A study on a proprioceptively deafferented subject , 2006, Brain Research Bulletin.

[58]  E. Ahissar,et al.  Parallel Thalamic Pathways for Whisking and Touch Signals in the Rat , 2006, PLoS biology.

[59]  Martin Deschênes,et al.  Feedforward Inhibitory Control of Sensory Information in Higher-Order Thalamic Nuclei , 2005, The Journal of Neuroscience.

[60]  B. Webb Neural mechanisms for prediction: do insects have forward models? , 2004, Trends in Neurosciences.

[61]  Martin Deschênes,et al.  Single‐cell study of motor cortex projections to the barrel field in rats , 2003, The Journal of comparative neurology.

[62]  Stephen H. Scott,et al.  Overlap of internal models in motor cortex for mechanical loads during reaching , 2002, Nature.

[63]  D. Kleinfeld,et al.  Adaptive Filtering of Vibrissa Input in Motor Cortex of Rat , 2002, Neuron.

[64]  Rune W. Berg,et al.  Coherent electrical activity between vibrissa sensory areas of cerebellum and neocortex is enhanced during free whisking. , 2002, Journal of neurophysiology.

[65]  A. Keller,et al.  Functional circuitry involved in the regulation of whisker movements , 2002, The Journal of comparative neurology.

[66]  Zoubin Ghahramani,et al.  Computational principles of movement neuroscience , 2000, Nature Neuroscience.

[67]  D. Wolpert,et al.  Why can't you tickle yourself? , 2000, Neuroreport.

[68]  D M Merfeld,et al.  Humans use internal models to estimate gravity and linear acceleration , 1999, Nature.

[69]  M. A. Goodale,et al.  The role of visual feedback of hand position in the control of manual prehension , 1999, Experimental Brain Research.

[70]  D. Wolpert,et al.  Internal models in the cerebellum , 1998, Trends in Cognitive Sciences.

[71]  D Kleinfeld,et al.  Central versus peripheral determinants of patterned spike activity in rat vibrissa cortex during whisking. , 1997, Journal of neurophysiology.

[72]  M. Brecht,et al.  Functional architecture of the mystacial vibrissae , 1997, Behavioural Brain Research.

[73]  R. Parenti,et al.  The Projections of the Lateral Reticular Nucleus to the Deep Cerebellar Nuclei. An Experimental Analysis in the Rat , 1996, The European journal of neuroscience.

[74]  C. Bard,et al.  Control of single-joint movements in deafferented patients: evidence for amplitude coding rather than position control , 1996, Experimental Brain Research.

[75]  Michael I. Jordan,et al.  An internal model for sensorimotor integration. , 1995, Science.

[76]  J. Billard,et al.  The interposito-rubrospinal system. Anatomical tracing of a motor control pathway in the rat , 1987, Neuroscience Research.

[77]  D. Sparks,et al.  Corollary discharge provides accurate eye position information to the oculomotor system. , 1983, Science.

[78]  B J Richmond,et al.  Vision during saccadic eye movements. II. A corollary discharge to monkey superior colliculus. , 1980, Journal of neurophysiology.

[79]  N. Tsukahara,et al.  Physiological properties of the newly formed cortico-rubral synapses of red nucleus neurons due to collateral sprouting , 1976, Brain Research.

[80]  R. Bowden,et al.  The functional significance of the pattern of innervation of the muscle quadratus labii superioris of the rabbit, cat and rat. , 1956, Journal of anatomy.

[81]  P. Cz. Handbuch der physiologischen Optik , 1896 .

[82]  Internal Models , 2020, Encyclopedia of Creativity, Invention, Innovation and Entrepreneurship.

[83]  G. Aston-Jones,et al.  Methylphenidate modifies the motion of the circadian clock Lamotrigine in mood disorders and cocaine dependence Cortical glutamate in postpartum depression CNO Evil ? Considerations for the Use of DREADDs in Behavioral Neuroscience , 2018 .

[84]  Fan Wang,et al.  The Brainstem Oscillator for Whisking and the Case for Breathing as the Master Clock for Orofacial Motor Actions. , 2014, Cold Spring Harbor symposia on quantitative biology.

[85]  N. Tsukahara,et al.  Sprouting of cortico-rubral synapses in red nucleus neurones after destruction of the nucleus interpositus of the cerebellum , 2005, Experientia.

[86]  B. Komisaruk,et al.  Difference in projections to the lateral and medial facial nucleus: anatomically separate pathways for rhythmical vibrissa movement in rats , 2004, Experimental Brain Research.

[87]  E. Dietrichs,et al.  An ipsilateral projection from the red nucleus to the lateral reticular nucleus in the cat , 2004, Anatomy and Embryology.

[88]  Rune W. Berg,et al.  Rhythmic whisking by rat: retraction as well as protraction of the vibrissae is under active muscular control. , 2003, Journal of neurophysiology.

[89]  David Kleinfeld,et al.  Closed-loop neuronal computations: focus on vibrissa somatosensation in rat. , 2003, Cerebral cortex.

[90]  D Kleinfeld,et al.  Anatomical loops and their electrical dynamics in relation to whisking by rat. , 1999, Somatosensory & motor research.

[91]  J. Azerad,et al.  Reciprocal connections between the red nucleus and the trigeminal nuclei: a retrograde and anterograde tracing study. , 1998, Physiological research.

[92]  M. Jacquin,et al.  Trigeminal orosensation and ingestive behavior in the rat. , 1983, Behavioral neuroscience.

[93]  W. Welker,et al.  Coding of somatic sensory input by vibrissae neurons in the rat's trigeminal ganglion. , 1969, Brain research.

[94]  W. Welker Analysis of Sniffing of the Albino Rat 1) , 1964 .