### Abstract

Response properties of vertical (VC) and horizontal (HC) canal/otolith- convergent vestibular nuclei neurons were studied in decerebrate rats during stimulation with sinusoidal linear accelerations (0.2-1.4 Hz) along different directions in the head horizontal plane. A novel characteristic of the majority of tested neurons was the nonzero response often elicited during stimulation along the 'null' direction (i.e., the direction perpendicular to the maximum sensitivity vector, S(max)). The tuning ratio (S(min) gain/S(max) gain), a measure of the two-dimensional spatial sensitivity, depended on stimulus frequency. For most vestibular nuclei neurons, the tuning ratio was small at the lowest stimulus frequencies and progressively increased with frequency. Specifically, HC neurons were characterized by a flat S(max) gain and an approximately 10-fold increase of S(min) gain per frequency decade. Thus, these neurons encode linear acceleration when stimulated along their maximum sensitivity direction, and the rate of change of linear acceleration (jerk) when stimulated along their minimum sensitivity direction. While the S(max) vectors were distributed throughout the horizontal plane, the S(min) vectors were concentrated mainly ipsilaterally with respect to head acceleration and clustered around the nasooccipital head axis. The properties of VC neurons were distinctly different from those of HC cells. The majority of VC cells showed decreasing S(max) gains and small, relatively flat, S(min) gains as a function of frequency. The S(max) vectors were distributed ipsilaterally relative to the induced (apparent) head tilt. In type I anterior or posterior VC neurons, S(max) vectors were clustered around the projection of the respective ipsilateral canal plane onto the horizontal head plane. These distinct spatial and temporal properties of HC and VC neurons during linear acceleration are compatible with the spatiotemporal organization of the horizontal and the vertical/torsional ocular responses, respectively, elicited in the rat during linear translation in the horizontal head plane. In addition, the data suggest a spatially and temporally specific and selective otolith/canal convergence. We propose that the central otolith system is organized in canal coordinates such that there is a close alignment between the plane of angular acceleration (canal) sensitivity and the plane of linear acceleration (otolith) sensitivity in otolith/canal-convergent vestibular nuclei neurons.

Original language | English (US) |
---|---|

Pages (from-to) | 1403-1417 |

Number of pages | 15 |

Journal | Journal of Neuroscience |

Volume | 13 |

Issue number | 4 |

State | Published - Jan 1 1993 |

### Fingerprint

### Keywords

- convergence
- eye movements
- linear acceleration
- otolith
- otolith-ocular reflex
- spatial tuning
- vestibular
- vestibulo-ocular reflex

### ASJC Scopus subject areas

- Neuroscience(all)

### Cite this

*Journal of Neuroscience*,

*13*(4), 1403-1417.

**Two-dimensional spatiotemporal coding of linear acceleration in vestibular nuclei neurons.** / Angelaki, Dora; Bush, G. A.; Perachio, A. A.

Research output: Contribution to journal › Article

*Journal of Neuroscience*, vol. 13, no. 4, pp. 1403-1417.

}

TY - JOUR

T1 - Two-dimensional spatiotemporal coding of linear acceleration in vestibular nuclei neurons

AU - Angelaki, Dora

AU - Bush, G. A.

AU - Perachio, A. A.

PY - 1993/1/1

Y1 - 1993/1/1

N2 - Response properties of vertical (VC) and horizontal (HC) canal/otolith- convergent vestibular nuclei neurons were studied in decerebrate rats during stimulation with sinusoidal linear accelerations (0.2-1.4 Hz) along different directions in the head horizontal plane. A novel characteristic of the majority of tested neurons was the nonzero response often elicited during stimulation along the 'null' direction (i.e., the direction perpendicular to the maximum sensitivity vector, S(max)). The tuning ratio (S(min) gain/S(max) gain), a measure of the two-dimensional spatial sensitivity, depended on stimulus frequency. For most vestibular nuclei neurons, the tuning ratio was small at the lowest stimulus frequencies and progressively increased with frequency. Specifically, HC neurons were characterized by a flat S(max) gain and an approximately 10-fold increase of S(min) gain per frequency decade. Thus, these neurons encode linear acceleration when stimulated along their maximum sensitivity direction, and the rate of change of linear acceleration (jerk) when stimulated along their minimum sensitivity direction. While the S(max) vectors were distributed throughout the horizontal plane, the S(min) vectors were concentrated mainly ipsilaterally with respect to head acceleration and clustered around the nasooccipital head axis. The properties of VC neurons were distinctly different from those of HC cells. The majority of VC cells showed decreasing S(max) gains and small, relatively flat, S(min) gains as a function of frequency. The S(max) vectors were distributed ipsilaterally relative to the induced (apparent) head tilt. In type I anterior or posterior VC neurons, S(max) vectors were clustered around the projection of the respective ipsilateral canal plane onto the horizontal head plane. These distinct spatial and temporal properties of HC and VC neurons during linear acceleration are compatible with the spatiotemporal organization of the horizontal and the vertical/torsional ocular responses, respectively, elicited in the rat during linear translation in the horizontal head plane. In addition, the data suggest a spatially and temporally specific and selective otolith/canal convergence. We propose that the central otolith system is organized in canal coordinates such that there is a close alignment between the plane of angular acceleration (canal) sensitivity and the plane of linear acceleration (otolith) sensitivity in otolith/canal-convergent vestibular nuclei neurons.

AB - Response properties of vertical (VC) and horizontal (HC) canal/otolith- convergent vestibular nuclei neurons were studied in decerebrate rats during stimulation with sinusoidal linear accelerations (0.2-1.4 Hz) along different directions in the head horizontal plane. A novel characteristic of the majority of tested neurons was the nonzero response often elicited during stimulation along the 'null' direction (i.e., the direction perpendicular to the maximum sensitivity vector, S(max)). The tuning ratio (S(min) gain/S(max) gain), a measure of the two-dimensional spatial sensitivity, depended on stimulus frequency. For most vestibular nuclei neurons, the tuning ratio was small at the lowest stimulus frequencies and progressively increased with frequency. Specifically, HC neurons were characterized by a flat S(max) gain and an approximately 10-fold increase of S(min) gain per frequency decade. Thus, these neurons encode linear acceleration when stimulated along their maximum sensitivity direction, and the rate of change of linear acceleration (jerk) when stimulated along their minimum sensitivity direction. While the S(max) vectors were distributed throughout the horizontal plane, the S(min) vectors were concentrated mainly ipsilaterally with respect to head acceleration and clustered around the nasooccipital head axis. The properties of VC neurons were distinctly different from those of HC cells. The majority of VC cells showed decreasing S(max) gains and small, relatively flat, S(min) gains as a function of frequency. The S(max) vectors were distributed ipsilaterally relative to the induced (apparent) head tilt. In type I anterior or posterior VC neurons, S(max) vectors were clustered around the projection of the respective ipsilateral canal plane onto the horizontal head plane. These distinct spatial and temporal properties of HC and VC neurons during linear acceleration are compatible with the spatiotemporal organization of the horizontal and the vertical/torsional ocular responses, respectively, elicited in the rat during linear translation in the horizontal head plane. In addition, the data suggest a spatially and temporally specific and selective otolith/canal convergence. We propose that the central otolith system is organized in canal coordinates such that there is a close alignment between the plane of angular acceleration (canal) sensitivity and the plane of linear acceleration (otolith) sensitivity in otolith/canal-convergent vestibular nuclei neurons.

KW - convergence

KW - eye movements

KW - linear acceleration

KW - otolith

KW - otolith-ocular reflex

KW - spatial tuning

KW - vestibular

KW - vestibulo-ocular reflex

UR - http://www.scopus.com/inward/record.url?scp=0027513230&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=0027513230&partnerID=8YFLogxK

M3 - Article

C2 - 8463828

AN - SCOPUS:0027513230

VL - 13

SP - 1403

EP - 1417

JO - Journal of Neuroscience

JF - Journal of Neuroscience

SN - 0270-6474

IS - 4

ER -