Abstract
It is reported that CNS hemorrage causes membrane dysfunction and may exacerbate this damage as a result of secondary ischemia or hypoxia. Since hyperbaric oxygenation improves oxygen metabolism, it may reduce this membrane damage. The present study was conducted to reveal whether hyperbaric oxygenation influences membrane alteration after hemorrhage. Thirty minutes after subarachnoid hemorrhage induction, rats were treated with hyperbaric oxygenation 2 ATA for 1 hour. Rats were decapitated 2 hours after subarachnoid hemorrhage induction. Na+, K+-ATPase activity measurement, and spin-label studies were performed on crude synpatosomal membranes. Subarachnoid hemorrhage decreased Na+, K+-ATPase activity. Spin label studies showed that hydrophobic portions of near the membrane surface became more rigid and the mobility of the membrane protein labeled sulfhydryl groups decreased after subarachnoid hemorrhage. Hyperbaric oxygenation significantly ameliorated most of the subarachnoid hemorrhage induced alterations. We conclude that hyperbaric oxygenation may be a beneficial treatment for acute subarachnoid hemorrhage.
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Miller, J. D., and Sullivan, H. 1979. Severe intracranial hypertension. Int-Anesthesiol-Clin. 17:19–75.
Neubauer, R. A., and End, E. 1980. Hyperbaric oxygenation as an adjunct therapy in strokes due to thrombosis: a review of 122 patients. Stroke 11:297–304.
Sukoff, M. H., and Ragatz, R. E. 1982. Hyperbaric oxygenation for the treatment of acute cerebral edema. Neurosurgery 10:29–38.
Kawamura, S., Ohta, H., Yasui, N., Nemoto, M., Hinuma, Y., and Suzuki, E. 1984. Effects of hyperbaric oxygenation in patients with subarachnoid hemorrhage evaluated with somatosensory evoked potentials. Pages 159–163, in Jacobson, J. H. (eds.), Proceedings of the Eighth International Congress on Hyperbaric Medicine, Best Publishing Company, San Pedolo.
Hubschmann, O. R., and Kornhauser, D. 1982. Effect of subarachnoid hemorrhage on the extracellular microenvinronment. J. Neurosurg. 56:216–221.
Hubschmann, O. R., and Nathanson, D. C. 1985. The role of calcium and cellular membrane dysfunction in experimental trauma and subarachnoid hemorrhage. J. Neurosurg. 62:698–703.
Marzatico, F. M., Gaetani, P., Rodriguez y Baena, R., Silavani, V., Paoletti, P., and Benzi, G. 1988. Bioenergetics of different brain areas after experimental subarachnoid hemorrhage in rats. Stroke 19:378–384.
Fischer, B., Jain, K. K., Braun, E., and Lehrl, S. 1988. chapter 14. hyperbaric oxygenation in disorders of the nervous system. Pages 134–175. in Fischer, B., Jain, K. K., Braun, E., Lehrl, S., (eds.), Handbook of hyperbaric oxygen theraphy, Springer-Verlag, Berlin Heiderberg.
Solomon, R. A., Antunes, J.L., Chen, R. Y. Z., Bland, L., and Chien, S. 1985. Decrease in cerebral blood flow in rats after experimental subarachnoid hemorrhage: a new animal model. Stroke 16:58–64.
Kamada, K. 1991. Experimental studies of cerebral blood gas changes with acute increased intracranial pressure under high pressure. Jpn. J. Hyperbar. Med. 26:65–74.
Glowinski, J., and Iversen, L. L. 1966. Regional studies of catecholamines in the rat brain—I. J. Neurochem. 13:665–669.
Gray, E. G., and Whittaker, V. P. 1962. The isolation of nerve endings from brain: an electron-microscopic study of cell fragments derived by homogenization and centrifugation. J. Anat. 96:79–87.
Leong, S. F., and Leung, T. K. C. 1991. Diabetes induced by streptozotocin causes reduced Na−K ATPase in the brain. Neurochem. Res. 16:1161–1165.
Nagy, K., Floyd, R., Simon, P., and Nagy, I. Z. 1985. Studies on the effect of iron overload on rat cortex synaptosomal membranes. Biochim. Biophys. Acta 820:216–222.
Eletr, S., and Inesi, G. 1972. Phase changes in the lipid moieties of sarcoplasmic reticulum membranes induced by temperature and protein conformational changes. Biochim. Biophys. Acta 290:178–185.
Hubbell, W. L., and McConnel, H. M. 1971. Molecular Motion in Spin-Labeled Phospholipids and Membranes. J. Am. Chem. Soc. 93:314–326.
Butterfield, D. A., Roses, A. D., Appel, S. H., and Chesnut, D. B. 1976. Electron spin resonance studies of membrane proteins in erythrocytes in myotonic muscular dystrophy. Arch. Biochem. Biophys. 177:226–234.
Chong, P. L. G., Fortes, P. A. G., and Jameson, D. M. 1985. Mechanisms of Inhibition of (Na,K)-ATPase by Hydrostatic Pressure Studied with Fluorescent Probes. J. Biol. Chem. 260:14484–14490.
Kimelberg, H. K., and Papahadjopoulos, D. 1972. Phospholipid requirement for (Na++K+)-ATPase activity: head-group specificity and fatty acid fluidity. Biochim Biophys. Acta 282:277–292.
Sandermann Jr., H. 1978. Regulation of membrane enzyme by lipids. Biochim. Biophys. Acta. 515:209–237.
Bralet, J., Beley, P., Jemaa, R., Bralet, A. M., and Beley, A. 1987. Lipid metabolism, cerebral metabolic rate, and some related enzyme activities after brain infarction in rats. Stroke 18:418–425.
Dagani, F., and Erecínska, M. 1987. Relationships among ATP synthesis, K+ gradients, and neurotransmitter amino acid levels in isolated rat brain synpatosomes. J. Neurochem. 49:1229–1240.
MacMillan, V. 1982. Cerebral Na+, K+-ATPase activity during exposure to and recovery from acute ischemia. J. Cereb. Blood Flow Metab. 2:457–465.
Nagy, K., Simon, P., and Zs.-Nagy, I. 1983. Spin label studies on synaptosomal membranes of rat brain cortex during aging. Biochim. Biophys. Res. Com. 117:688–694.
Zaleska-M., M., Nagy, K., and Floyd, R. A. 1989. Iron-induced lipid peroxidation and inhibition of dopamine synthesis in striatum synaptosomes. Neurochem. Res. 14:597–605.
Keith, A. D., Sharnoff, M., and Cohn, G. E. 1973. A summary and evaluation of spin labels used as probes for biological membrane structure. Biochim. Biophys. Acta. 300:379–419.
Schreier, S., Polnaszek, C. F., and Smith I. C. P. 1978. Spin labels in membranes: problems in practice. Biochim. Biophys. Acta. 515:375–436.
Sandberg, H. E., Bryant, R. G., and Piette, L. H. 1969. Studies on the location of sulfhydryl groups in erythrocyte membranes with magnetic resonance spin probes. Arch. Biochem. Biophys. 133:144–152.
Chien, K. R., Abrams, J., Serroni, A., Martin, J. T., and Farber, J.L. 1978. Accelerated phospholipid degradation and associated membrane dysfunction in irreversible, ischemic liver cell Injury. J. Biol. Chem. 253:4809–4817.
Gaetani, P., Marzatico, F., Rodriguez y Baena, R., Pacchiarini, L., Vigano, T., Grignani, G., Crivellari, M. T., and Benzi, G. 1990. Arachidonic Acid Metabolism and Pathophysiologic Aspects of Subarachnoid Hemorrhage in Rats. Stroke 21:328–332.
Marzatico, F., Gaetani, P., Rodriguez y Baena, R., Silvani, V., Fulle, I., Lombardi, D., Ferlenga, P., and Benzi, G. 1989. Experimental subarachnoid hemorrhage. Lipid peroxidation and Na+, K+-ATPase in different rat brain areas. Mol. Chem. Neuropathol 11:99–107.
Dana, J., and van den Brenk, H. A. S. 1963. Measurement of oxygen tensions in cerebral tissues of rats exposed to high pressures of oxygen. J. Appl. Physiol. 18:869–876.
White, P. F., Johnston, R. R., and Pudwill, C. R. 1975. Interaction of ketamine and halothane in rats. Anesthesiology 42:179–186.
Davis, D. W., Mans, A. M., Biebuyck, J. F., and Hawkins, R. A. 1988. The influence of ketamine on regional brain glucose use. Anesthesiology 69:199–205.
Dedrick, D. F., Scherer, Y. D., and Biebuyck, J. F. 1975. Use of a rapid brain-sampling technique in a physiologic preparation: Effects of morphine, ketamine, and halothane on tissue energy intermediates. Anesthesiology 42:651–657.
Sakaki, S., Ohta, S., Nakamura, H., and Takeda, S. 1988. Free radical reaction and biological defense mechanism in the pathogensis of prolonged vasospasm in experimental subarachnoid hemorrhage. J. Cereb. Blood Flow Metab. 8:1–8.
Watanabe, T., Sasaki, T., Asano, T., Takakura, K., Sano, K., Fuchinoue, T., Watanabe, K., Yoshimura, S., and Abe, K. 1988. Changes in glutathione peroxidase and lipid peroxides in cerebrospinal fluid and serum after subarachnoid hemorrhage: with special reference to the occurrence of cerebral vasospasm. Neurol. Med. Chir. (Tokyo). 28:645–649.
Noda, Y., McGeer, P. L., and McGeer, E. G. 1983. Lipid peroxide distribution in brain and the effect of hyperbaric oxygen. J. Neurochem. 40:1329–1332.
Mishra, O. P., Delivoria-Papadopoulos, M., Chaillane, G., and Wagerle, L. C. 1989. Lipid peroxidation as the mechanism of modification of the affinity of the Na+, K+-ATPase active sites for ATP, K+, Na+, and Strophanthidin in vitro. Neurochem. Res. 14:845–851.
Viani, P., Cervato, k G., Fiorilli, A., and Cestaro, B. 1991. Agerelated differences in synaptosomal peroxidative damage and membrane properties. J. Neurochem. 56:253–8.
Sadrzadeh, S. M. H., Graf, E., Panter, S. S., Hallaway, P. E., and Eaton, J. W. 1984. Hemoglobin: a biologic Fenton reagent. J. Biol. Chem. 259:14354–14356.
Sadrzadeh, S. M. H., Anderson, D. K., Panter, S. S., Hallaway, P. E., and Eaton, J. W. 1987. Hemoglobin potentiates central nervous system damage. J. Clin. Invest. 79:662–664.
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Yufu, K., Itoh, T., Edamatsu, R. et al. Effect of hyperbaric oxygenation on the Na+, K+-ATPase and membrane fluidity of cerebrocortical membranes after experimental subarachnoid hemorrhage. Neurochem Res 18, 1033–1039 (1993). https://doi.org/10.1007/BF00966765
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DOI: https://doi.org/10.1007/BF00966765