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Cerebrospinal fluid and extracellular fluid: their relationship to pressure and duration of canine hydrocephalus

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Abstract

Fifteen greyhound dogs were made hydrocephalic by the transsphenoidal injection of silicone into the basal cisterns at the level of the tentorial incisura. Six of these animals had ventriculocisternal perfusions 4 weeks later and six at 8 weeks, half at 150 and half at 100 mm H2O. Three 12-week dogs were perfused at 150 mm H2O. Serial sections of brain from the ependyma of the left frontal horn to the overlying pia were counted for14C inulin and3H methotrexate uptake. Tissue concentrations of both markers varied indirectly with distance from ependyma and from pia, and varied directly with perfusion pressure. The data indicate that the diffusional pathway between cere-brospinal fluid (CSF) and extracellular fluid (ECF) can be modified by CSF pressure changes, i.e., CSF flows from the ventricles and subarachnoid space into the extracellular space when CSF pressures are raised. Brain uptake of inulin and methotrexate was significantly increased in the dogs made hydrocephalic 4 weeks prior to perfusion, but was less so in the 8-week hydrocephalics. Uptake of the tracers in three 12-week animals was similar to that found previously in normal dogs at elevated pressures. These findings correspond in location and time to the periventricular lucencies that are seen by computed tomography in human subacute hydrocephalus. They are apparently due to pressure-related changes in the volume of the ECF.

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References

  1. Bering EA, Sata O (1963) Hydrocephalus: changes in formation and absorption of CSF within the cerebral ventricles. J Neurosurg 20:1050–1063

    Google Scholar 

  2. Blasberg RG, Patlak CS, Shapiro WR (1977) Distribution of MTX in the CSF and brain after intraventricular administration. Cancer Treat Rep 61:633–641

    Google Scholar 

  3. Brightman MW (1967) The intracerebral movement of proteins injected into blood and cerebrospinal fluid of mice. Prog Brain Res 29:19–37

    Google Scholar 

  4. Cserr HF, Cooper DN, Milhorat TH (1977) Flow of cerebral interstitial fluid as indicated by the removal of extracellular markers from rat caudate nucleus. Exp Eye Res [Suppl] 25:461–473

    Google Scholar 

  5. Cutler RWP, Barlow CF, Lorenzo AV (1967) The effect of brain-CSF diffusion gradients on the determination of ECS in cat brain. J Neuropathol Exp Neurol 26:167–169

    Google Scholar 

  6. Davson H, Welch K (1971) The permeations of several materials into the fluids of the rabbit's brain. J Physiol (Lond) 218:337

    Google Scholar 

  7. Davson H, Kleeman CF, Levin E (1963) The blood-brain barrier. In: Proceedings of the 1rst International Pharmacological Meetings, vol 4. Pergamon, Oxford, pp 71–94

    Google Scholar 

  8. Elliot KAC, Jasper HH (1949) Physiological salt solutions for brain surgery. J Neurosurg 6:140–152

    Google Scholar 

  9. Feldberg W, Fleischhauer K (1960) Penetration of bromophenol blue from the perfused cerebral ventricles into the brain tissue. J Physiol (Lond) 150:451–462

    Google Scholar 

  10. Fishman RA, Greer M (1963) Changes in the cerebrum associated with experimental obstructive hydrocephalus. Arch Neurol 8:156–171

    Google Scholar 

  11. Johanssen CE, Flotz FM, Thompson AM (1974) The clearance of urea and sucrose from isotonic and hypertonic fluids perfused through the ventriculocisternal system. Exp Brain Res 20:18–31

    Google Scholar 

  12. Katzman R, Graziani L, Kaplan R, Escriva A (1965) Exchange of CSF potassium with blood and brain. Arch Neurol 13:513–524

    Google Scholar 

  13. Kimmelberg HK, Ring D, Watson RE, Reiss FL, Biddlecome SM, Bourke RS (1978) Direct administration of methotrexate into the CNS of primates. J Neurosurg 48:883–894

    Google Scholar 

  14. Levin VA, Fenstermacher JD, Patlak CS (1970) Sucrose and inulin space measurements of cerebral cortex in four mammalian species. Am J Physiol 219:1528–1533

    Google Scholar 

  15. Lux WE Jr, Hochwald GM, Sahar A, Ransohoff J (1970) Periventricular water content. Effect of pressure in experimental chronic hydrocephalus. Arch Neurol 23:475–479

    Google Scholar 

  16. McLone DG, Bondaroff W, Raimondi AJ (1971) Brain edema in the hydrocephalic HY-3 mouse: submicroscopic morphology. J Neuropathol Exp Neurol 30:627–637

    Google Scholar 

  17. Milhorat TH (1969) Choroid plexus and cerebrospinal fluid production. Science 166:1514–1516

    Google Scholar 

  18. Milhorat TH, Clark RG, Hammocks MK, McGrath PP (1970) Structural, ultrastructural, and permeability changes in the ependyma and surrounding brain favoring equilibration in progressive hydrocephalus. Arch Neurol 22:397–407

    Google Scholar 

  19. Naidich TP, Epstein F, Lin JP, Kricheff II, Hochwald GM (1976) Evaluation of pediatric hydrocephalus by computed tomography (D.S.). Radiology 119:337–345

    Google Scholar 

  20. Page LK (1984) The relationship between cerebrospinal fluid and brain extracellular fluid in normal and hydrocephalic dogs. In: Shapiro K, Marmarou A, Portnay H (eds) Hydrocephalus. Raven Press, New York, pp 109–120

    Google Scholar 

  21. Page LK, White WP (1981) Transsphenoidal injection of silicone for the production of communicating or obstructive hydrocephalus in dogs. Surg Neurol 17:247–250

    Google Scholar 

  22. Pollay M, Kaplan RJ (1971) Effect of the CSF sink on sucrose diffusion gradients in the brain. Exp Neurol 30:54–65

    Google Scholar 

  23. Protig PJ, Sharman DF, Vogt M (1968) Release by tubocurarine of dopamine and homovanillic acid from the superfused caudate nucleus. J Physiol (Lond) 194:565–572

    Google Scholar 

  24. Rall DP, Oppelt WW, Patlak CS (1962) Extracellular space of brain as determined by diffusion of inulin from the ventricular system. Life Sci 1:43–48

    Google Scholar 

  25. Reed DJ, Woodbury DM (1963) Kinetics of movement of iodine, sucrose, inulin and radio-iodinated serum albumin in the CNS and CSF of the rat. J Physiol (Lond) 169:816–850

    Google Scholar 

  26. Reulen HJ, Graham R, Spatz M, Klatzo I (1977) Role of pressure gradients and bulk flow in dynamics of vasogenic brain edema. J Neurosurg 46:24–35

    Google Scholar 

  27. Rothman AR, Freireich EJ, Gaskins JR, Patlak CS, Rall DP (1961) Exchange of inulin and dextran between blood and CSF. Am J Physiol 201:1145–1148

    Google Scholar 

  28. Rubin R, Owens E, Rall D (1968) Transport of methotrexate by the choroid plexus. Cancer Res 28:689–694

    Google Scholar 

  29. Sheard MH, Zolovick AJ (1971) Serotonin: release in cat brain and CSF on stimulation of midbrain Raphe'. Brain Res 26:445–458

    Google Scholar 

  30. Wald A, Hochwald GM, Gandhi M (1978) Evidence for the movement of fluid macromolecules and ions from the brain extracellular space to the CSF. Brain Res 151:283–290

    Google Scholar 

  31. Weed LH (1914c) Studies on cerebrospinal fluid. IV. The dual source of cerebrospinal fluid. J Med Res 31:93–113

    Google Scholar 

  32. Welch K, Sadler K (1966) Permeability of the choroid plexus of the rabbit to several solutes. Am J Physiol 210:652–660

    Google Scholar 

  33. Woodward DL, Reed DJ, Woodbury DM (1967) Extracellular space of rat cerebral cortex. Am J Physiol 212:367–370

    Google Scholar 

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Page, L.K. Cerebrospinal fluid and extracellular fluid: their relationship to pressure and duration of canine hydrocephalus. Child's Nerv Syst 1, 12–17 (1985). https://doi.org/10.1007/BF00706724

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