Journal of Neurophysiology · 2008 · 54 citations · 41 references
External InputsMotor ControlSocial SciencesNeural MechanismKinesiologySensory NeuroscienceNeurodynamicsTrigeminal Ganglion NeuronsHealth SciencesSensorimotor ControlSensorimotor IntegrationNervous SystemAwake RatsNeurobiological MechanismNeurophysiologyNeuroanatomyActive SensingPhysiologySensorimotor TransformationNeuroscienceCentral Nervous System
Active sensing requires the brain to distinguish signals produced by external inputs from those generated by the animal's own movements. Because the rodent whisker musculature lacks proprioceptors, we asked whether trigeminal ganglion neurons encode the kinematics of the rat's own whisker movements in air. By examining the role of kinematics, we have extended previous findings showing that many neurons that respond during such movements do not do so consistently. Nevertheless, the majority ( approximately 70%) of trigeminal ganglion neurons display significant correlations between firing rate and a kinematic parameter, and a subset, approximately 30%, represent kinematics with high reliability. Preferential firing to movement direction was observed but was strongly modulated by movement amplitude and speed. However, in contrast to the precise time-locking that occurs in response to active whisker contacts, whisker movements in air generate temporally dispersed responses that are not time-locked to the onset of either protractions or retractions.
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Spike-triggered neural characterization
Odelia Schwartz, Jonathan W. Pillow, Nicole C. Rust et al. · Journal of Vision · 2006 · 455 citations · Full text
Cognitive Science, Instantaneous Firing Rate, Neurodynamics +12