Control of orienting gaze shifts by the tectoreticulospinal system in the head-free cat. III. Spatiotemporal characteristics of phasic motor discharges
- PMID: 1765799
- DOI: 10.1152/jn.1991.66.5.1642
Control of orienting gaze shifts by the tectoreticulospinal system in the head-free cat. III. Spatiotemporal characteristics of phasic motor discharges
Abstract
1. In this paper we describe the movement-related discharges of tectoreticular and tectoreticulospinal neurons [together called TR (S) Ns] that were recorded in the superior colliculus (SC) of alert cats trained to generate orienting movements in various behavioral situations; the cats' heads were either completely unrestrained (head free) or immobilized (head fixed). TR (S) Ns are organized into a retinotopically coded motor map. These cells can be divided into two groups, fixation TR (S) Ns [f TR (S) Ns] and orientation TR (S) Ns [oTR(S)Ns], depending on whether they are located, respectively, within or outside the zero (or area centralis) representation of the motor map in the rostral SC. 2. oTR(S)Ns discharged phasic motor bursts immediately before the onset of gaze shifts in both the head-free and head-fixed conditions. Ninety-five percent of the oTR(S)Ns tested (62/65) increased their rate of discharge before a visually triggered gaze shift, the amplitude and direction of which matched the cell's preferred movement vector. For movements along the optimal direction, each cell produced a burst discharge for gaze shifts of all amplitudes equal to or greater than the optimum. Hence, oTR(S)Ns had no distal limit to their movement fields. The timing of the burst relative to the onset of the gaze shift, however, depended on gaze shift amplitude: each TR(S)N reached its peak discharge when the instantaneous position of the visual axis relative to the target (i.e., instantaneous gaze motor error) matched the cell's optimal vector, regardless of the overall amplitude of the movement. 3. The intensity of the movement-related burst discharge depended on the behavioral context. For the same vector, the movement-related increase in firing was greatest for visually triggered movements and less pronounced when the cat oriented to a predicted target, a condition in which only 76% of the cells tested (35/46) increased their discharge rate. The weakest movement-related discharges were associated with spontaneous gaze shifts. 4. For some oTR(S)Ns, the average firing frequency in the movement-related burst was correlated to the peak velocity of the movement trajectory in both head-fixed and head-free conditions. Typically, when the head was unrestrained, the correlation to peak gaze velocity was better than that to either peak eye or head velocity alone. 5. Gaze shifts triggered by a high-frequency train of collicular microstimulation had greater peak velocities than comparable amplitude movements elicited by a low-frequency train of stimulation.(ABSTRACT TRUNCATED AT 400 WORDS)
Similar articles
-
Control of orienting gaze shifts by the tectoreticulospinal system in the head-free cat. II. Sustained discharges during motor preparation and fixation.J Neurophysiol. 1991 Nov;66(5):1624-41. doi: 10.1152/jn.1991.66.5.1624. J Neurophysiol. 1991. PMID: 1765798
-
Control of orienting gaze shifts by the tectoreticulospinal system in the head-free cat. I. Identification, localization, and effects of behavior on sensory responses.J Neurophysiol. 1991 Nov;66(5):1605-23. doi: 10.1152/jn.1991.66.5.1605. J Neurophysiol. 1991. PMID: 1765797
-
Fixation and orientation control by the tecto-reticulo-spinal system in the cat whose head is unrestrained.Rev Neurol (Paris). 1989;145(8-9):567-79. Rev Neurol (Paris). 1989. PMID: 2554460
-
How visual inputs to the ponto-bulbar reticular formation are used in the synthesis of premotor signals during orienting.Prog Brain Res. 1989;80:159-70; discussion 127-8. doi: 10.1016/s0079-6123(08)62209-8. Prog Brain Res. 1989. PMID: 2699363 Review.
-
Studies of the role of the paramedian pontine reticular formation in the control of head-restrained and head-unrestrained gaze shifts.Ann N Y Acad Sci. 2002 Apr;956:85-98. doi: 10.1111/j.1749-6632.2002.tb02811.x. Ann N Y Acad Sci. 2002. PMID: 11960796 Review.
Cited by
-
Post-spike facilitation of neck EMG by cat tectoreticulospinal neurones during orienting movements.J Physiol. 1995 Jan 15;482 ( Pt 2)(Pt 2):455-66. doi: 10.1113/jphysiol.1995.sp020532. J Physiol. 1995. PMID: 7714836 Free PMC article.
-
Effects of caudate nucleus stimulation on substantia nigra cell activity in monkey.Exp Brain Res. 1993;95(3):457-72. doi: 10.1007/BF00227139. Exp Brain Res. 1993. PMID: 8224072
-
Modeling eye-head gaze shifts in multiple contexts without motor planning.J Neurophysiol. 2016 Oct 1;116(4):1956-1985. doi: 10.1152/jn.00605.2015. Epub 2016 Jul 20. J Neurophysiol. 2016. PMID: 27440248 Free PMC article.
-
Adult plasticity of spatiotemporal receptive fields of multisensory superior colliculus neurons following early visual deprivation.Restor Neurol Neurosci. 2010;28(2):259-70. doi: 10.3233/RNN-2010-0488. Restor Neurol Neurosci. 2010. PMID: 20404413 Free PMC article.
-
Monocular visual activation patterns in albinism as revealed by functional magnetic resonance imaging.Hum Brain Mapp. 2004 Sep;23(1):40-52. doi: 10.1002/hbm.20046. Hum Brain Mapp. 2004. PMID: 15281140 Free PMC article.
Publication types
MeSH terms
LinkOut - more resources
Full Text Sources
Miscellaneous