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Saccades reduce latency and increase velocity of ocular accommodation.

Horizontal vergence can be stimulated binocularly with disparity (disparity vergence) or monocularly with accommodation (accommodative vergence). The latter results from a neural cross-coupling that causes both horizontal vergence and accommodation to respond when either one is stimulated [Alpern, M., & Ellen, P. (1956). American Journal of Ophthalmology, 42, 289-303]. The velocity of disparity and accommodative vergence is enhanced when accompanied by saccades [Enright, J. T. (1984). Journal of Physiology (London) 350, 9-31; Enright, J. T. (1986). Journal of Physiology (London) 371, 69-89]. Based upon the coupling between accommodation and vergence, we predicted that accommodation should also be facilitated by saccades. An SRI Dual Purkinje Eyetracker was used to measure left and right eye position, and the accommodation of the left eye, in response to stimulation. Horizontal saccades were stimulated by targets separated by 2-6 degrees and accommodation was stimulated monocularly over a range of +/- 2 diopters (D). When saccades occurred within 0-400 ms following a monocular step stimulus to accommodation, latency of accommodation decreased and the associated accommodative-vergence response was synchronized with the saccade. Saccades also enhanced the velocity of accommodation and accommodative-vergence, and this facilitation increased with saccade amplitude. Transient vergence responses that are normally associated with saccades [Erkelens, C. J., Steinman, R. M., & Collewijn, H. (1989). Proceedings of the Royal Society of London B. Biological Sciences, 236, 441-465; Maxwell, J. S., & King, W. M. (1992). Journal of Neurophysiology, 68 (4), 1248-1260] did not affect accommodation when it was not stimulated by defocus. Because saccades and accommodation utilize separate plants and final common pathways, the synchronization of saccades and accommodation and the enhanced velocity of accommodation and accommodative-vergence must occur at more central sites. Possibilities include the superior colliculus, which represents both accommodation and saccades [Nagasaka, Y., & Ohtsuka, K., (1998). Investigative Ophthalmology AVRO supplement], vestibular nuclei which project to regions near the oculomotor nuclei [Lang, W., Buttner-Ennever, J. A., & Buttner, U. (1979). Brain Research, 177, 3-17], and interactions between omni pause neurons and near response cells of the mesencephalic reticular formation (MRF) [Mays, L. E., & Gamlin, P. D. R. (1995a). Current Opinions in Neurobiology, 5, 763-768; Mays, L. E., & Gamlin, P. D. R. (1995b). Eye movement research: Mechanisms, processes and applications. New York: Elsevier] which represent both accommodation and vergence [Judge, S. J., & Cumming, B. G. (1986). Journal of Neurophysiology, 55, 915-930; Zhang, Y., Mays, L. E., & Gamli, P. D. R. (1992). Journal of Neurophysiology, 67, 944-960].

Accommodation, Ocular↗

Subcortical neural circuits for ocular accommodation and vergence in primates.

Our current knowledge of the neural bases of vergence and accommodation has increased significantly over the past few years. The behavior of medial rectus motoneurons during vergence, which has been reported by a number of investigators, is described. The behavior of Edinger-Westphal neurons during accommodation is also described, as are the characteristics of midbrain near-response neurons in the supraoculomotor area. Evidence that some of these near-response neurons provide the vergence input to medial rectus motoneurons and possibly the accommodation input to Edinger-Westphal neurons is reviewed. Anatomical studies have shown that the midbrain near-response region receives input from two deep cerebellar nuclei, the posterior interposed and the fastigial nucleus. Single-unit recording in the posterior interposed nucleus has revealed cells that increase their activity during the far-response, and the behavior of these neurons is reviewed. In addition, studies of a precerebellar nucleus, the nucleus reticularis tegmenti pontis, have revealed some cells that increase their activity during the near-response and others that do so during the far-response. The behavior of these neurons is reviewed. This review documents the great strides that are occurring in our understanding of the anatomy and physiology of the neural pathways controlling vergence and accommodation in the primate.

Accommodation, Ocular↗

Ocular accommodation, personality, and autonomic balance.

The autonomic nervous system is made up of two subsystems: the parasympathetic (PNS) and the sympathetic (SNS). The balance between these systems regulates bodily functions during routine (PNS-dominant) and crisis (SNS-dominant) situations. It may also control visual accommodation: PNS activation for inward focus, and SNS activation for outward focus. Near- and far-sighted persons have been characterized as introverted and extraverted, respectively. These personality characteristics have been linked to autonomic balance: introversion and PNS-dominance, extraversion and SNS-dominance. Because autonomic balance may influence accommodation, the introversion of near-sighted and the extraversion of far-sighted persons may be related to the more general PNS-SNS balance rather than only to the difference in visual functioning. Research relevant to this hypothesis is reviewed.

Accommodation, Ocular↗

Cortical indices of impaired ocular accommodation and associated convergence mechanisms.

The accommodative and fusional vergence mechanisms were examined electrophysiologically in a juvenile suffering from a severe reduction in focusing ability. We used the visually evoked response (VER) to diagnose the accommodation-vergence insufficiency. The procedure is shown to be effective for monitoring longitudinally the ability of simple orthoptic techniques to restore normal accommodative function.

Accommodation, Ocular↗

Ultrasound measures of vitreous chamber depth during ocular accommodation.

The vitreous chamber decreased in depth about 0.12 mm as accommodative demand increased from 0.2 to 7 D in nine accommodative steps. The depth decreases matched movement of the posterior lens surface toward the retina. Accommodation caused no significant increases in axial length compared to cyclopleged controls. These results do not favor the active role for the vitreous in accommodation proposed by Coleman in 1970. Computer analysis of A-scan interval counts demonstrated that multiple retinal complex peaks might erroneously point to vitreous or axial lengthening. About 30% of total lens thickening during accommodation was accounted for by posterior lens surface displacement.

Accommodation, Ocular↗

Spectral bandwidth and ocular accommodation.

Previous studies have suggested that targets illuminated by monochromatic (narrow-band) light are less effective in stimulating the eye to change its focus than are black-white (broadband) targets. The present study investigates the influence of target spectral bandwidth on the dynamic accommodation response in eight subjects. The fixation target was a 3.5-cycle/deg square-wave grating illuminated by midspectral light of various bandwidths [10, 40, and 80 nm and white (CIE Illuminant B)]. The target was moved sinusoidally toward and away from the eye, and accommodation responses were recorded and Fourier analyzed. Accommodative gain increases, and phase lag decreases, with increasing spectral bandwidth. Thus the eye focuses more accurately on targets of wider spectral bandwidth. The visual system appears to have the ability to analyze polychromatic blur to determine the state of focus of the eye for the purpose of guiding the accommodation response.

Accommodation, Ocular↗

Using diplopia as a warning of an inappropriate visual (ocular) accommodative response (WIVAR).

BACKGROUND: Over-accommodation, a tendency to focus at a distance closer than the desired distance, has been previously shown to occur when using a head-up display (HUD). METHODS: A simple system was developed as a warning of an inappropriate visual accommodative response (WIVAR) during flight training. Two lines, which are seen as four low-contrast lines (physiological diplopia) if the user is focused in the distance due to the link between convergence and accommodation, are projected onto the pilot's HUD combiner. RESULTS: The results show that by using the WIVAR system the accommodative response can be kept more distant when viewing forward-looking infra-red imagery (by 0.12 +/- 0.04 D; p < 0.05), performing a high cognitive workload task (by 0.07 +/- 0.03 D; p < 0.05) and especially when viewing in a Ganzfeld (by 0.41 +/- 0.12 D; p < 0.01). CONCLUSION: While collimated HUD imagery stimulates the user to a more distant focus, the use of the WIVAR lines can cause additional relaxation of accommodation.

Accommodation, Ocular↗

[Effect of noise on ocular accommodation].

The goal of investigations was the determination of connection between the level of noise and the extra-auditory reaction of the organism--a change of the near point. Changes of accommodation determined by means of a black-and-white check-board test were monitored in the course and after 1 hour exposition to noise of 90 dB-A, 93 dB-A, 96 dB-A or 99 dB-A of the sound level. The results show that the deterioration of vision is a complicated exponential function of the intensity and time of the exposition to noise.

Accommodation, Ocular↗

Vestibular influences on ocular accommodation in cats.

Electrical stimulation of the utricle in C-1 transected cats (whose labyrinths remained sensitive to natural stimulation) induced bilateral pupillary dilatation and bilateral 0.4 to 3.0 diopter lens change in an anti-accommodative direction. Both effects could still be induced two weeks after cutting the ipsilateral cervical sympathetic trunk. It is concluded that these effects take place by inhibiting the parasympathetic pathway originating in the Edinger-Westphal nucleus. The mediating pathways from the vestibular complex to the Edinger-Westphal nucleus pass through the brain stem in the region outside the medial longitudinal fasciculi.

Accommodation, Ocular↗