Changes in cerebral blood flow and distribution associated with acute increases in plasma sodium and osmolality of chronic hyponatremic rats

Experimental Neurology

Volumn 163, Issue 1, 2000, Pages 63-71

  Adler, Sheldon ^a   Verbalis, Joseph G ^b   Meyers, Susan ^a   Simplaceanu, Elena ^c   Williams, Donald S ^c  

^a UNIVERSITY OF PITTSBURGH SCHOOL OF MEDICINE   (United States)

^b GEORGETOWN UNIVERSITY SCHOOL OF MEDICINE   (United States)

^c CARNEGIE MELLON UNIVERSITY   (United States)

Author keywords

Blood brain barrier; Cerebral perfusion; Demyelination; Magnetic resonance flow imaging

Indexed keywords

CARBON DIOXIDE; SODIUM;

ANIMAL CELL; ANIMAL EXPERIMENT; ANIMAL TISSUE; ARTICLE; BLOOD BRAIN BARRIER; BRAIN BLOOD FLOW; CONTROLLED STUDY; DEMYELINATION; HYPONATREMIA; MALE; NONHUMAN; NUCLEAR MAGNETIC RESONANCE; OSMOLALITY; PRIORITY JOURNAL; RAT; SODIUM BLOOD LEVEL;

EID: 0034107291     PISSN: 00144886     EISSN: None     Source Type: Journal    
DOI: 10.1006/exnr.2000.7376     Document Type: Article

References (41)

1. Abdul-Rahman A., Dahlgren N., Johanesson B. B., Siesjo B. O. K. Increases in local cerebral blood flow induced by circulating adrenaline: Involvement of blood-brain barrier dysfunction. Acta Physiol. Scand. 107:1979;226-232.
2. Adler S., Verbalis J. G. Effect of hypertonic saline infusion on cerebral perfusion in normonatremic and hyponatremic rats. Soc. Neurosci. Abstr. 29:1994.
3. Adler S., Verbalis J. G., Williams D., Martinez A. J. Relationship between demyelination (DM) and blood brain barrier (BBB) disruption following rapid correction of hyponatremia. Soc. Neurosci. Abstr. 22:1996.
4. Adler S., Williams D., Verbalis J. G. Effect of acute and chronic hyponatremia on blood brain barrier function in the rat. NMR Biomed. 6:1993;119-124.
5. Adler S., Martinez A. J., Williams D. S., Verbalis J. G. Positive association between blood brain barrier disruption and osmotically-induced demyelination. Multiple Sclerosis. 6:2000;24-31.
6. Belova T. I., Johnson G. Blood-brain barrier permeability and immobilization stress. Acta Physiol. Scan. 116:1982;21-29.
7. Berl T. Treating hyponatremia: Damned if we do and damned if we don't. Kidney Int. 37:1990;1006-1018.
8. Bruhwyler J., Chleide E., Keogeosi J. G., Carreer F. Nitric oxide: A new messenger in the brain. Neurosci. Behavioral Res. 17:1993;363-384.
9. Compston A., Scolding N., Wren D., Noble M. The pathogenesis of demyelinating disease: Insights from cell biology. TINS. 14:1991;175-182.
10. Constable P. D., Muri W. W. III, Binkley P. F. Hypertonic saline is a negative isotropic agent in normovolumic dogs. Am. J. Physiol. 267:1994;H667-H677.
11. Deakin A. M., Payne A. N., Whittle B. J., Moncada S. The modulation of IL-2 and TNF-alpha release by nitric oxide following stimulation of J774 cells with LPS and IFN-gamma. Cytokine. 7:1995;408-416.
12. Dinarello C. A., Gelfand J. A., Wolff S. M. Anticytokine strategies in the treatment of the systemic inflammatory response syndrome. J. Am. Med. Assoc. 269:1993;1829-1835.
13. Ginsberg M. D. Autoradiographic measurement of local cerebral blood flow. Wood J. H. Cerebral Blood Flow: Physiologic and Clinical Aspects. 1987;299-308 McGraw-Hill, New York.
14. Gjedde A., de la Monte S. M., Caronna J. J. Cerebral blood flow and oxygen consumption in rat measured with microspheres or Xenon. Acta Physiol. Scand. 100:1977;273-281.
15. Grundl P. D., Biagas K. V., Kochanek P. M., Schiding A. J. K., Barmada M. A., Nemoto E. M. Early cerebrovascular response to head injury in immature and mature rats. J. Neurotrauma. 11:1994;135-148.
16. Hansen T. D., Warner D. S., Todd M. M., Vust L. T. Effects of nitrous oxide and volatile anesthetics on cerebral blood flow. Br. J. Anaesthesiol. 63:1989;290-295.
17. Hartung H. P., Jung S., Stoll G., Zielasak J., Schmidt B., Archelos J. J. U. Inflammatory mediators in demyelinating disorders of the CNS and PNS. J. Neuroimmunol. 40:1992;194-210.
18. Hemmingsen R., Hertz M. M., Barry D. I. The effect of propranolol on cerebral oxygen consumption and blood flow in the rat: Measurements during normocapnia and hypercapnia. Acta Physiol. Scand. 105:1979;274-281.
19. Henderson L. Ultrafiltration with peritoneal dialysis. Nolph K. D. Peritoneal Dialysis. 1985;162-177 Kluwer, Kornrecht.
20. Iadecola C., Pelligrino D. A., Moskowitz M. A., Lessen N. A. Nitric oxide synthase inhibition and cerebrovascular regulation. J. Cereb. Blood Flow Metab. 14:1994;175-192.
21. Pappius H. M., Savaki H. E., Fieschi C., Rapoport S. I., Sokoloff L. Osmotic opening of the blood-brain barrier and local cerebral glucose utilization. Ann. Neurol. 5:1970;211-219.
22. Pellerin L., Magistretti P. J. Glutamate uptake into astrocytes stimulates aerobic glycolysis: A mechanism coupling neuronal activity to glucose utilization. Proc. Natl. Acad. Sci. USA. 91:1994;10625-10629.
23. Pickard J. D. Role of prostaglandins and arachidonic acid derivatives in the coupling of cerebral blood flow to cerebral metabolism. J. Cereb. Blood Flow Metab. 1:1981;361-384.
24. Robinson P. J. Measurement of blood-brain barrier permeability. Clin. Exp. Pharmacol. Physiol. 17:1990;829-840.
25. Scolding N. J., Morgan B. P., Houston A., Campbell A. K., Linington C., Compston D. A. S. Normal rat serum cytotoxicity against syngeneic oligodendrocytes: Complement activation and attack in the absence of anti-myelin antibodies. J. Neurol. Sci. 89:1989;289-300.
26. Sharief M. K., Thompson E. J. In vivo relationship of tumor necrosis factor-alpha to blood-brain barrier damage in patients with active multiple sclerosis. J. Neuroimmunol. 38:1992;27-34.
27. Sterns R. H., Capuccio J. D., Silver S. M., Cohen E. P. Neurologic sequelae after treatment of severe hyponatremia: A multicenter perspective. J. Am. Soc. Nephrol. 4:1994;1522-1530.
28. Sterns R. H., Riggs J. E., Schocker S. S. Osmotic demyelination syndrome following correction or hyponatremia. N. Engl. J. Med. 314:1986;1535-1542.
29. Strandgaard S., Panlson O. B. Regulation of cerebral blood flow in health and disease. J. Cardiovas. Pharmacol. 19:1992;589-539.
30. Toda N., Ayajiki J., Okamura T. Hypercapnia relaxes cerebral arteries and potentiates neurally-induced relaxation. J. Cereb. Blood Flow Metab. 16:1996;1068-1074.
31. Vanguri P., Kolski C. L., Silverman B., Shin M. L. Complement activation by isolated myelin: Activation of the classical pathway in the absence of myelin specific antibodies. Proc. Natl. Acad. Sci. USA. 79:1982;3290-3294.
32. Vara E., Arias-Diza J., Garcia C., Hernandez T., Balibra J. T. TNF-alpha-induced inhibition of PC synthesis by human type II pneumocytes is sequentially mediated by PGE2 and NO. Am. J. Physiol. 271:1996;L359-L365.
33. Verbalis J. G., Drutarosky M. D. Adaptation to chronic hypoosmolality in rats. Kidney Int. 34:1988;351-360.
34. Verbalis J. G., Martinez A. J. Neurological and neuropathological sequelae of controlled correction of hypoosmolality in chronically hyponatremic rats. Kidney Int. 39:1991;1274-1282.
35. Verbalis J. G., Baker E. A., Tian Y., Adler S. Immunocytochemical evidence in support of blood brain barrier disruption and complement activation in the brain following rapid correction of chronic hyponatremia in rats. Soc. Neurosci. Abstr. 23:1997;886.3.
36. Verbalis J. G., Gullan S. R. Rapid correction of hyponatremia produces differential effects on brain osmolyte and electrolyte reaccumulation in rats. Brain Res. 606:1993;19-27.
37. Warner D. S., Kassell N. F., Boarini D. J. Microsphere cerebral blood flow determination. Wood J. H. Cerebral Blood Flow: Physiologic and Clinical Aspects. 1987;288-296 McGraw-Hill, New York.
38. Williams D. S., Detre J. D., Leigh J. S., Koretsky A. P. Magnetic resonance imaging of perfusion using spin inversion of arterial water. Proc. Natl. Acad. Sci. USA. 89:1992;212-216.
39. Wing M. G., Zajicke J., Seilly D. J., Compston D. A., Lachman P. J. Oligodendrocytes lack glycolipid anchored proteins which protect them against complement lysis: Restoration of resistance to lysis by incorporation of CD 59. Immunology. 76:1992;140-145.
40. Wren D. R., Noble M. Oligodendrocytes and oligodendrocyte/type-2 astrocyte progenitor cells of adult rats are specifically susceptible to the lytic effects of complement in the absence of antibody. Proc. Natl. Acad. Sci. USA. 86:1989;9025-9029.
41. Zhang W., Williams D. S., Koretsky A. P. Measurement of rat brain perfusion by NMR using spin labeling of arterial water in vivo determination of the degree of arterial spin labeling. Magn. Reson. Med. 29:1993;416-421.