Abstract
The aperture of the refracting system of the eye is controlled by the iris which behaves as a diaphragm, contracting or expanding as a result of the opposing actions of two muscles of ectodermal origin, namely the sphincter pupillae and the dilator pupillae. As classically described, the sphincter is an annular band of smooth muscle, 0.75 to 0.8 mm broad in man, encircling the pupillary border, which on contraction draws out the iris and constricts the pupillary aperture. At the pupillary border the muscle is closely associated with the pigment epithelium, so that, on contraction, the latter tends to be drawn on to the anterior surface of the iris. The sphincter is closely adherent to the adjacent connective tissue so that, after an iridectomy, it does not contract up, and the pupil remains reactive to light. Like the sphincter, the dilator muscle is of ectodermal origin, but in the sphincter the ectodermal cells have been transformed into true muscle fibres whereas the cells of the dilator retain their primitive characteristics and are called myoepithelial cells.
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References
Akert, K., Glicksman, M. A., Lang, W., Grob, P. & Huber, A. (1980) The Edinger-Westphal nucleus in the monkey. A retrograde tracer study. Brain Res. 184, 491–498.
Alexandridis, E. & Koeppe, E. R. (1969) Die spektrale Empfindlichkeit der für den Pupillenlichtreflex verantwortlichen Photoreceptoren beim Menschen. v. Graefs’ Arch. Ophthal. 177, 136–151.
Alpern, M. & Campbell, F. W. (1962) The spectral sensitivity of the consensual light reflex. J. Physiol. 164, 478–507.
Bennett, D. R., Reinke, D. A., Alpert, E., Baum, T. & Vasquez-Leon, H. (1961) The action of intraocularly administered adrenergic drugs on the iris. J. Pharmacol. 134, 190–198.
Bonvallet, M. & Zbrozyna, A. (1963) Les commandes reticulaires du système autonome et en particulier de l’innervation sympathique de la pupille. Arch. Ital. Biol. 101, 174–207.
Castiglioni, A. J., Gallaway, M. C. & Coulter, J. D. (1978) Spinal projections from the midbrain in monkey. J. Comp. Neurol. 178, 329–346.
Cavaggioni, A., Madarasz, I. & Zampollo, A. (1968) Photic reflex and pretectal region. Arch. ital. Biol. 106, 227–240.
De Groot, S. G. & Gebhard, J. W. (1952) Pupil size as determined by adapting luminance. J. Opt. Soc. Am. 42, 492–495.
Ehinger, B., Falck, B. & Persson, H. (1968) Function of cholinergic nerve fibres in the cat iris dilator. Acta Physiol. Scand. 72, 139–147.
Hartmann-von Monakow, K., Akert, K. & Künzle, H. (1979) Projections of precentral and premotor cortex to the red nucleus and other midbrain areas. Exp. Brain Res. 34, 91–105.
Hess, W. R. (1957) The Functional Organizatio of the Diencephalon. New York: Grune & Stratton.
Hultborn, H., Mori, K. & Tsukahara, N. (1978a) The neuronal pathway subserving the pupillary light reflex. Brain Res. 159, 255–267.
Hultborn, H., Mori, K. & Tsukahara, N. (1978b) Cerebellar influence on parasympathetic neurones innervating intraocular muscles. Brain Res. 159, 269–278.
Ijichi, Y., Kiyohara, T., Hosoba, M. & Tsukahara, N. (1977) The cerebellar control of the pupillary light reflex in the cat. Brain Res. 128, 69–79.
Jampel, R. S. & Mindel, J. (1967) The nucleus for accommodation in the midbrain of the macaque. Invest. Ophthal. 6, 40–50.
Loewy, A. D., Saper, C. B. & Yamodis. (1978) Re-evaluation of the efferent projections of the Edinger-Westphal nucleus in the cat. Brain Res. 141, 153–159.
Lowenstein, O. & Loewenfeld, I. E. (1958) Electronic pupillography. Arch. Ophthal. 59, 352–363.
Lowenstein, O. & Loewenfeld, I. E. (1959a) Scotopic and photopic thresholds of the pupillary light reflex in normal man. Am. J. Ophthal. 48, pt. 2, 87–98.
Lowenstein, O. & Loewenfeld,\ I. E. (1959b) Influence of retinal adaptation upon the pupillary reflex to light in normal man. Am. J. Ophthal. 48, pt. 2, 536–550.
Lowenstein, O. & Loewenfeld, I. E. (1969) The Pupil. In The Eye, 2nd ed., Ed. Davson, Vol. III, pt. 2. London & New York: Academic Press.
Magoun, H. W. & Ranson, S. W. (1953) The central path of the light reflex. Arch. Ophthal. 13, 791–811.
Nishida, S. & Sears, M. (1969a) Fine structural innervation of the dilator muscle of the iris of the albino guinea pig studied with permanganate fixation. Exp. Eye Res. 8, 292–296.
Nishida, S. & Sears, M. (1969b) Dual innervation of the iris sphincter muscle of the albino guinea pig. Exp. Eye Res. 8, 467–469.
Passatore, M. (1976) Physiological characterization of efferent cervical sympathetic fibers influenced by changes of illumination. Exp. Neurol. 53, 71–81.
Passatore, M. & Pettorossi, V. E. (1976) Efferent fibers in the cervical sympathetic nerve influenced by light. Exp. Neurol. 52, 66–82.
Patil, P. N. (1969) Adrenergic receptors of the bovine iris sphincter. J. Pharmacol. 166, 299–307.
Pierson, R. J. & Carpenter, M. B. (1974) Anatomical analysis of pupillary reflex pathways in the rhesus monkey. J. comp. Neurol. 158, 121–143.
Richardson, K. C. (1964) The fine structure of the albino rabbit iris with special reference to the identification of adrenergic and cholinergic nerves and nerve endings in its intrinsic muscles. Am. J. Anat. 114, 173–184.
Scalia, F. (1972) The termination of retinal axons in the pretectal region of mammals. J. comp. Neurol. 145, 223–245.
Schweitzer, N. M. J. (1956) Threshold measurements on the light reflex of the pupil in the dark adapted eye. Doc. Ophthal. 10, 1–78.
Sillito, A. M. (1968) The location and activity of pupilloconstrictor neurones in the mid-brain of the cat. J. Physiol. 194, 39–40 P.
Sillito, A. M. & Zbrozyna, A. W. (1970) The localization of pupilloconstrictor function within the mid-brain of the cat. J. Physiol. 211, 461–477.
Smith, J. D., Masek, G. A., Ichinose, L. Y., Watanabe, T. & Stark, L. (1970) Single neuron activity in the pupillary system. Brain Res. 24, 219–234.
Stark, L., Campbell, F. W. & Atwood, J. (1958) Pupil unrest: an example of noise in a biological servomechanism. Nature, Lond. 182, 857–858.
Suzuki., R., Oso, T. & Kobayashi, S. (1983) Cholinergic inhibitory response in the bovine iris muscle. Invest. Ophthal. 24, 760–765.
Swanson, L. W., Cowan, W. M. & Jones, E. G. (1974). An autoradiographic study of the efferent connections of the ventral lateral geniculate nucleus in the albino rat and the cat. J. Comp. Neurol. 156, 143–163.
Toyoshima, K., Kawana, E. & Sakai, H. (1980) On the neuronal origin of the afferents to the ciliary ganglion in cat. Brain Res. 185, 67–76.
Van Alphen, G. W. H. M., Kern, R. & Robinette, L. (1965) Adrenergic receptors of the intraocular muscles. Arch. Ophthal. N.Y. 74, 253–259.
Van Alphen, G. W. H. M., Robinette, S. L. & Macri, F. J. (1964) The adrenergic receptors of the intraocular muscles of the cat. Int. J. Neuropharmacol. 2, 259–272.
Westheimer, G. & Blair, S. M. (1973) The parasympathetic pathways to internal eye muscles. Invest. Ophthal. 12, 193–197.
Yoshitomi, T. & Ito, Y. (1986) Pre-synaptic action of noradrenaline on the dog ciliary muscle tissue. Exp. Brain Res. 43, 119–127.
Yoshitomi, T., Ito, Y. & Inomata, H. (1985) Adrenergic excitatory and cholinergic inhibitory innervation in the human iris dilator. Exp. Eye Res. 40, 453–459.
Zhang, S. Q., Butler, J. M., Ohara, K. & Cole, D. F. (1982) Sensory neural mechanisms in contraction of the isolated sphincter pupillae: the role for substance P and the effects of sensory denervation on the response to miotics. Exp. Eye Res. 35, 43–54.
Zhang, S. Q., Butler, J. M. & Cole, D. F. (1984) Sensory neural mechanisms in contraction of the rabbit isolated sphincter pupillae: analysis of the responses to capsaicin and electrical field stimulation. Exp. Eye Res. 38, 153–163.
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© 1990 Hugh Davson
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Davson, H. (1990). The Pupil. In: Physiology of the Eye. Palgrave, London. https://doi.org/10.1007/978-1-349-09997-9_26
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DOI: https://doi.org/10.1007/978-1-349-09997-9_26
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