rotational stimulation
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2019 ◽  
Vol 2019.54 (0) ◽  
pp. 163
Author(s):  
Yuki KUROSAWA ◽  
Kenji KIKUCHI ◽  
Keiko NUMAYAMA ◽  
Takuji ISHIKAWA

2012 ◽  
Vol 148 (1) ◽  
pp. 176-177
Author(s):  
Faith W. Akin ◽  
Courtney D. Hall ◽  
Owen D. Murnane

2005 ◽  
Vol 37 (5-6) ◽  
pp. 379-387 ◽  
Author(s):  
G. Z. Mikhailova ◽  
N. R. Tiras ◽  
E. E. Grigor’yeva ◽  
D. A. Moshkov

2000 ◽  
Vol 10 (2) ◽  
pp. 93-98
Author(s):  
H. Fushiki ◽  
S. Takata ◽  
K. Yasuda ◽  
Y. Watanabe

We used optokinetic stimulation (OKS) in eighteen normal adults aged 18–30 years to investigate vertical self-motion perception. In order to induce self-rotation, either a stripe pattern or a random dot pattern was projected onto the inner wall of a hemispherical dome with a diameter of 150 cm. The pattern was rotated either about the subject’s vertical axis (yaw) or about the subject’s interaural axis (pitch) for 80 s at a constant acceleration of 1 deg / s 2 . Stimuli were randomly repeated three to four times in each direction. The latency of onset as well as the perceived intensity of circular vection (CV) was measured for each stimulus presentation. CV latencies for upward rotational stimulation were significantly longer than those for downward rotational stimulation under both types of stimulus conditions. There was no significant difference in CV latency between rightward and leftward rotational stimulation. For most subjects, the magnitudes of the perceived CV for rightward rotational stimulation were equal to those for leftward rotational stimulation, whereas the magnitudes of the perceived CV for vertical stimulation showed large intersubject variability. These results provide additional evidence that fundamental differences exist between different types of self-motion. Possible explanations for the directional asymmetry in vertical perception of self-motion will also be discussed.


1989 ◽  
Vol 62 (5) ◽  
pp. 1090-1101 ◽  
Author(s):  
J. D. Dickman ◽  
M. J. Correia

1. The horizontal semicircular canals of anesthetized (barbiturate/ketamine) pigeons were stimulated by rotational and by mechanical stimulation. 2. The mechanical stimulation consisted of making a small (less than 1 mm) fistula in the lateral part of the bony horizontal semicircular canal and, after inserting a probe coupled to a piezoelectric micropusher through the fistula, providing controlled indentation of the exposed membranous horizontal semicircular duct. 3. Extracellular action potentials from single horizontal semicircular canal primary afferent (HCA) fibers were recorded during sinusoidal rotational and during step, ramp, and sinusoidal mechanical stimulation. 4. The mean spontaneous discharge rate of 160 horizontal canal afferents was 86 +/- 4 (SE) spikes/s. This rate was not significantly different from that reported previously for pigeon HCA fibers recorded with the horizontal canal intact (i.e., no fistula introduced). 5. Sinusoidal mechanical indentation of the horizontal semicircular duct produced clearly entrained action potentials on 36 HCA fibers for a range of peak displacements from +/- 0.5 to +/- 30 microns. Action potentials were never modulated on afferents (n greater than 100) identified as innervating the anterior and posterior semicircular canals or the otolith organs during mechanical stimulation of the horizontal semicircular canal, even for displacements as large as 30 microns. 6. Intensity functions relating peak firing frequency (spikes per second) and peak probe displacement (micrometers) for 1.0-Hz sinusoidal mechanical stimulation were linear over the range 1.0-5.0 microns. The most sensitive units (6/36, 17%) showed response saturation as the stimulus magnitude was extended to 7 microns and beyond. 7. In 15 of 36 units, both mechanical and rotational sinusoidal stimulation (1.0 Hz) were applied to the same unit. The duct indentation magnitudes were 1.0, 2.5, 5.0, and 7.0 microns and the rotational velocities were 5, 10, and 20 deg/s. The constant of proportionality found to equate the peak response produced by rotational to that elicited by mechanical stimulation was 7.0 deg.sec-1/1.0 microns. 8. Bode plots and best-fit transfer functions of the frequency response (0.05-10.0 Hz) of 14 HCAs exposed to both mechanical and rotational stimulation were nearly identical. 9. Parameters for best-fit transfer functions, responses to step, and trapezoidal duct displacements were in excellent agreement with previous rotational studies carried out using the pigeon. 10. Although the mechanisms by which focal identation of the horizontal membranous duct produce responses have not yet been determined, primary afferent responses using this method of stimulation are directly comparable with rotatory stimulation.(ABSTRACT TRUNCATED AT 400 WORDS)


1988 ◽  
Vol 102 (1) ◽  
pp. 35-42 ◽  
Author(s):  
Brian L. Matthews ◽  
Kenneth A. Campbell ◽  
Sam A. Deadwyler

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