Abstract
Fifteen rabbits were intrathecally perfused with horseradish peroxidase at normal cerebrospinal fluid pressures. Horseradish peroxidase was found in the subarachnoid space around the optic nerve; it permeated the pia and penetrated within the nerve, occupying extracellular spaces between myelinated axons and glial cells up to the area of the lamina cribrosa. Horseradish peroxidase also crossed the perineural sclera and the border tissue of Elschnig to spread into the choroid where it was mostly seen within choriocapillaris, venules, and veins crossing through interendothelial spaces. “Bulk” cerebrospinal fluid absorption in the eye appears to occur through venous drainage in the choroid and SAS.
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References
Anderson DR, Hoyt WF (1969) Ultrastructure of intraorbital portion of human and monkey optic nerve. Arch Ophthalmol 82: 506–530
Bill A (1966) Routes for bulk drainage of aqueous humor in rabbits with and without cyclodialysis. Doc Ophthalmol 20: 157–162
Bill A (1971) Aqueous humor dynamics in monkeys (Maccaca iris and Cercopithecus Ethiops). Exp Eye Res 12: 195–206
Bradford FK, Johnson PC (1962) Passage of intact iron-labeled erythrocytes from subarachnoid space to systemic circulation in dogs. J Neurosurg 19: 332–336
Butler AB, Van Landingham K, McComb JG (1983) Pressure-facilitated CSF flow across the arachnoid membrane. In: Ishii S, Nagai H, Brock M (eds) Intracranial pressure, V. Springer, Berlin Heidelberg New York, pp 598–604
Casley-Smith JR, Foldi-Borcsok E, Foldi M (1976). The prelymphatic pathways of the brain as revealed by cervical lymphatic obstruction and the passage of particles. Br J Exp Pathol 57: 179–188
Cohen AI (1973) Is there a potential defect in the blood retinal barrier at the choroidal level of the optic nerve canal? Invest Ophthalmol 12: 513–519
Cunha-Vaz JG, Shakib M, Ashton N (1966) Studies on the permeability of the blood-retinal barrier. I. On the existence, development and site of a blood retinal barrier. Br J Ophthalmol 50: 441–453
Davson H (1967) Physiology of the cerebrospinal fluid. Churchill Livingstone, Edinburgh London New York
Davson H, Hollingsworth G, Segal MB (1970) The mechanism of drainage of the cerebrospinal fluid. Brain 93: 665–678
De La Motte DJ (1978) Removal of horseradish peroxidase and fluorescein-labeled dextran from CSF spaces of rabbit optic nerve. A light and electron microscope study. Exp Eye Res 27: 585–594
Faber WM (1937) The nasal mucosa and the subarachnoid space. Am J Anat 62: 121–148
Field EJ, Brierley JB (1947) The lymphatic drainage of the spinal nerve roots in the rabbit. J Anat 81: 198–207
Field EJ, Brierley JB (1949) The retro-orbital tissues as a site of outflow of cerebrospinal fluid. Proc R Soc Med 42: 447–550
Fine BS, Yanoff M (1979). Ocular histology, 2nd ed. Harper & Row, New York
Fishman RA (1971) Cerebrospinal fluid in diseases of the nervous system. Saunders, Philadelphia
Foldi M, Csillik B, Zoltan OT (1968) Lymphatic drainage of the brain. Experientia 24: 1283
Gomez DG, Potts DG, Deonarine V, Reilly KF (1973) Effect of pressure gradient changes on the morphology of the arachnoid villi and granulations of the monkey. Lab Invest 28: 648–657
Gomez DG, Fenstermacher J, Manzo RP, Johnson D, Potts DG (1985) Cerebrospinal fluid absorption in the rabbit: olfactory pathways. Acta Otolaryngol (Stockh) 100: 429–436
Grayson MC, Laties AM (1971) Ocular localization of sodium fluorescein. Arch Ophthalmol 85: 600–609
Hayreh SS (1977) Fluids in the anterior part of the optic nerve in health and disease. Trans Ophthalmol Soc UK 97: 573–587
Hayreh SS (1977) Optic disc edema in raised intracranial pressure V. Pathogenesis. Arch Ophthalmol 95: 1553–1565
Hogan JH, Alvarado JA, Weddell JE (1971) Histology of the human eye. Saunders, Philadelphia
Ivanow G (1927) Über die Abflußwege aus den submeningeulen Räumen des Rückenmarks, part 2. Ges Exp Med 58: 1–21
Ilberg CV, Arnold W (1977) Lymphatic drainage of the inner ear. In: Mayall RC, Witte MH (eds) Progress in lymphology. Plenum Press, New York, pp 55–56
Key EAG, Retzius G (1875–1876) Studien in der Anatomie des Nervensystems und des Bindegenebes. Samson and Wallin, Stockholm part 1: 1–220; part 2: 1–228
Leak LV, Burke JF (1968) Ultrastructural studies on the lymphatic anchoring filaments. J Cell Biol 36: 129–149
Mann JP, Butler AB, Rosenthal JE, Maffeo CJ, Johnson RN, Bass NH (1978) Regulation of intracranial pressure in rat, dog, and man. Ann Neural 3: 156–165
McComb JG (1983) Recent research into the nature of cerebrospinal fluid formation and absorption. J Neurosurg 59: 369–383
Nabeshima S, Reese TS, Landis DMD, Brightman MW (1975) Junctions in the meninges and marginal glia. J Comp Neurol 164: 127–170
Nakagawa Y, Cervos-Navarro J, Artigas J (1985) Tracer study on a paracellular route in experimental hydrocephalus. Acta Neuropathol (Berl) 65: 247–254
Ogata J, Hochwald GM, Gravioto H, Ransohoff J (1972) Distribution of intraventricular peroxidase in normal and hydrocephalic cat brains. J Neuropathol Exp Neurol 31: 454–463
Okinami S, Ohkuma M, Tsukahara I (1976). Kuhnt intermediary tissue as a barrier between optic nerve and retina. Graefes' Arch Clin Exp Ophthalmol 201: 57–67
Peyman GA, Apple D (1972) Peroxidase diffusion processes in the optic nerve. Arch Ophthalmol 88: 650–654
Quincke H (1972) Zur Physiologie der Cerebrospinalflüssigkeit. Arch Anat Physiol (Leipzig), pp 153–157
Raviola G, Butler JM (1983) Unidirectional vesicular transport mechanism in retinal vessels. Invest Ophthalmol Vis Sci 24: 1465–1474
Rennels ML, Gregory TF, Blaumanis OR, Fujimoto T, Grady PA (1984) Evidence for a paravascular fluid circulation in the mammalian central nervous system, provided by the rapid distribution of tracer protein throughout the brain from the subarachnoid space. Brain Res 326: 47–63
Rhodin JAG (1968) Ultrastructure of mammalian venous capillaries, venules, and small collecting veins. J Ultrastruct Mol Struct Res 25: 452–500
Rodriguez-Peralta LA (1966) Hematic and fluid barriers in the optic nerve. J Comp Neurol 126: 109–122
Rodriguez-Peralta LA (1968) Hematic and fluid barriers of the retina and vitreous body. J Comp Neurol 132: 109–117
Schutta HS, Hedges TR (1971) Fine structure observations on experimental papilledema in the Rhesus monkey. J Neurol Sci 12: 1–14
Siebenman F (1894) Die Blutgefässe im Labyrinthe des menschlichen Ohres. Berkman, Wiesbaden
Simionescu N, Simionescu M, Palade GE (1978) Open junctions in the endothelium of the postcapillary venules of the diaphragm. J Cell Biol 79: 27–44
Tso MOM, Fine BS (1976) Electron microscopy study of human papilledema. Ophthalmology 82: 424–434
Tso MOM, Hayreh SS (1977) Optic disk edema in raised intracranial pressure. III. A pathologic study of experimental papilledema. Arch Ophthalmol 95: 1448–1457
Tso MOM, Shih CY, McLean IW (1975) Is there a blood brain barrier at the optic nerve head? Arch Ophthalmol 93: 815–825
Tsukahara I, Yamashita H (1975) An electron microscopic study in the blood-optic nerve and fluid-optic nerve barrier. Graefes' Arch Clin Exp Ophthalmol 196: 239–246
Van Deurs B (1977) Vesicular transport of horseradish peroxidase from brain to blood in segments of the cerebral microvasculature in adult mice. Brain Res 124: 1–8
Wagner HJ, Piggrim C, Brandl J (1974) Penetration and removal of horseradish peroxidase injected into the cerebrospinal fluid. Acta Neuropathol 27: 299–315
Worthen DM (1978). Intraocular pressure and its diurnal variation. In: Heilman K, Richardson KT (eds) Concepts of a disease. Saunders, Philadelphia, pp 54–66
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This work was supported by NIH Grant RO1 NS13844
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Gomez, D.G., Manzo, R.P., Fenstermacher, J.D. et al. Cerebrospinal fluid absorption in the rabbit. Graefe's Arch Clin Exp Ophthalmol 226, 1–7 (1988). https://doi.org/10.1007/BF02172707
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DOI: https://doi.org/10.1007/BF02172707