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Effects of antioxidants on the blood-brain barrier and postischemic hyperemia

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Summary

The role of free oxygen radicals in blood-brain barrier (BBB) disruption and postischemic hyperemia was evaluated in the rabbit model of focal cerebral ischemia-reperfusion.

Six groups of rabbits underwent clipping of the anterior cerebral, middle cerebral, and intracranial internal carotid arteries. Cerebral blood flow (CBF) was measured by using radiolabeled microspheres, before, during, and 15 minutes after 1-hour occlusion of these arteries. After 50 minutes of ischemia, Group 1 animals (control) received a placebo. Animals in Groups 2–4 received one of three drugs: catalase at 10 mg/kg, methimazole at 5 mg/kg, or indomethacin at 10 mg/kg. A fifth group received a tungsten-supplemented diet for 14 days before ischemia was induced, and a sixth group was sham operated. Microvascular integrity within the brain was determined by the presence or absence of Evan's Blue (EB)-albumin dye leakage across the BBB and was measured by microspectrofluorometry.

In the control group during ischemia, CBF dropped to 14%, 7%, and 11% of preischemic levels in rostral, middle, and caudal sections of the brain, respectively, as characterized by extensive EB-albumin dye leakage through the BBB into the ischemic hemisphere. During early reperfusion, postischemic hyperemia was associated with an increase in CBF of 128%, 123%, and 129% of control in the rostral, middle, and caudal sections of the brain, respectively. In all treated groups and in the group receiving a tungsten-supplemented diet, BBB integrity was protected during reperfusion without inhibition of postischemic hyperemia.

This study suggests that early disruption of the BBB to large molecules is mediated by free oxygen radicals, which inhibit rather than cause postischemic hyperemia.

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References

  1. Adkins WK, Taylor AE (1990) Role of xanthine oxidase and neutrophils in ischemia/reperfusion injury in rabbit lung. J Appl Physiol 69: 2012–2018

    PubMed  Google Scholar 

  2. Ager A, Gordon JL (1984) Differential effects of hydrogen peroxide on indices of endothelial cell function. J Exp Med 159: 592–603

    PubMed  Google Scholar 

  3. Asano T, Shigeno T, Johshita H, Usui M, Hanamura T (1987) A novel concept on the pathogenic mechanism underlying ischaemic brain oedema: relevance of free radicals and eicosanoids. Acta Neurochir (Wien) [Suppl] 41: 85–96

    Google Scholar 

  4. Balazs C, Kiss E, Leovey A, Farid NR (1986) The immunosuppressive effect of methimazole on cell-mediated immunity is mediated by its capacity to inhibit peroxidase and to scavenge free oxygen radicals. Clin Endocrinol (Oxf) 25: 7–16

    Google Scholar 

  5. Betz AL, Randall J, Martz D (1991) Xanthine oxidase is not a major source of free radicals in focal cerebral ischemia. Am J Physiol 260: H 563-H 568

    Google Scholar 

  6. Busto R, Dietrich WD, Globus MY-T, Valdés I, Scheinberg P, Ginsberg MD (1987) Small differences in intraischemic brain temperature critically determine the effect of ischemic neuronal injury. J Cereb Blood Flow Metab 7: 729–738

    PubMed  Google Scholar 

  7. Cohen G, Heikkila RE, Allis B, Cabbat F, Dembiec D, MacNamee D, Mytilineou C, Winston B (1976) Destruction of sympathetic nerve terminals by 6-hydroxydopamine: protection by 1-phenyl-3-(2-thiozyl)-2-thiourea, diethyldithiocarbamate, methimazole, cysteamine, ethanol and n-butanol. J Pharmacol Exp Ther 199: 336–352

    PubMed  Google Scholar 

  8. Dempsey RJ, Roy MW, Meyer KL, Donaldson DL (1985) Indomethacin-mediated improvement following middle cerebral artery occlusion in cats: effects of anesthesia. J Neurosurg 62: 874–881

    PubMed  Google Scholar 

  9. Dumuis A, Sebben M, Haynes L, Pin JP, Bockaert J (1988) NMDA receptors activate the arachidonic acid cascade system in striatal neurons. Nature 336: 68–70

    PubMed  Google Scholar 

  10. Gottesfeld Z, Garcia CJ, Chronister RB (1987) Perinatal, not adult, hypothyroidism suppresses dopaminergic axon sprouting in the deafferented olfactory tubercle of the adult rat. J Neurosci Res 18: 568–573

    PubMed  Google Scholar 

  11. Hallenbeck JM, Furlow TW Jr (1979) Prostaglandin l2, and indomethacin prevent impairment of post-ischemic brain reperfusion in the dog. Stroke 10: 629–637

    PubMed  Google Scholar 

  12. Hatashita S, Hoff JT (1990) Brain edema and cerebrovascular permeability during cerebral ischemia in rats. Stroke 21: 582–588

    PubMed  Google Scholar 

  13. Helfaer MA, Kirsch JR, Haun SE, Moore LE, Traystman RJ (1991) Polyethylene glycol-conjugated Superoxide dismutase fails to blunt postischemic reactive hyperemia. Am J Physiol 261: H 548-H 553

    Google Scholar 

  14. Heymann MA, Payne BD, Hoffman JIE, Rudolph AM (1977) Blood flow measurements with radionuclide-labeled particles. Prog Cardiovasc Dis 20: 55–79

    PubMed  Google Scholar 

  15. Ito U, Ohno K, Nakamura R, Suganuma F, Inaba Y (1979) Brain edema during ischemia and after restoration of blood flow. Measurement of water, sodium, potassium content and plasma protein permeability. Stroke 10: 542–547

    PubMed  Google Scholar 

  16. Ito U, Ohno K, Yamaguchi T, Takei H, Tomita H, Inaba Y (1980) Effect of hypertension on blood-brain barrier. Change after restoration of blood flow in post-ischemic gerbil brains. An electron microscopic study. Stroke 11: 606–611

    PubMed  Google Scholar 

  17. Johansson B, Nilsson B (1977) The pathophysiology of the blood-brain barrier dysfunction induced by severe hypercapnia and by epileptic brain activity. Acta Neuropathol (Berl) 38: 153–158

    Google Scholar 

  18. Johnson JL, Rajagopalan KV, Cohen HJ (1974) Molecular basis of the biological function of molybdenum. Effect of tungsten on xanthine oxidase and sulfite oxidase in the rat. J Biol Chem 249: 859–866

    PubMed  Google Scholar 

  19. Johshita H, Asano T, Hanamura T, Takakura K (1989) Effect of indomethacin and a free radical scavenger on cerebral blood flow and edema after cerebral artery occlusion in cats. Stroke 20: 788–794

    PubMed  Google Scholar 

  20. Kadota E (1988) Regional cerebral blood flow (rCBF) pattern analysis corresponds with albumin extravasation in experimental cerebral ischemia. Neurol Res 10: 225–231

    PubMed  Google Scholar 

  21. Kontos HA (1989) Oxygen radicals in cerebral ischemia. In: Ginsberg MD, Dietrich WD (eds) Cerebrovascular diseases, Vol 16. Raven, New York, pp365–371

    Google Scholar 

  22. Kraaier V, Van Huffelen AC, Wieneke GH, Van der Worp HB, BÄr PR (1992) Quantitative EEG changes due to cerebral vasoconstriction. Indomethacin versus hyperventilation-induced reduction in cerebral blood flow in normal subjects. Electroencephalogr Clin Neurophysiol 82: 208–212

    PubMed  Google Scholar 

  23. Marshall JJ, Kontos HA (1990) Endothelium-derived relaxing factors. A perspective from in vivo data. Hypertension 16: 371–386

    PubMed  Google Scholar 

  24. Ment LR, Stewart WB, Duncan CC, Scott DT, Lambrecht R (1983) Beagle puppy model of intraventricular hemorrhage: effect of indomethacin on cerebral blood flow. J Neurosurg 58: 857–862

    PubMed  Google Scholar 

  25. Norins NA, Wendelberger K, Hoffman RG, Keller PA, Madden JA (1992) Effects of indomethacin on myogenic contractile activation and responses to changes in O2 and CO2 in isolated feline cerebral arteries. J Cereb Blood Flow Metab 12: 866–872

    PubMed  Google Scholar 

  26. Olsson Y, Crowell RM, Klatzo I (1971) The blood-brain barrier to protein tracers in focal cerebral ischemia and infarction caused by occlusion of the middle cerebral artery. Acta Neuropathol (Berl) 18: 89–102

    Google Scholar 

  27. Palluy O, Bonne C, Modat G (1991) Hypoxial/reoxygenation alters endothelial prostacyclin synthesis-protection by superoxide dismutase. Free Radic Biol Med 11: 269–275

    PubMed  Google Scholar 

  28. Patt A, Harken AH, Burton LK, Rodell TC, Piermattei D, Schorr WJ, Parker NB, Berger EM, Horesh IR, Terada LS, Linas SL, Cheronis JC, Repine JE (1988) Xanthine oxidase-derived hydrogen peroxide contributes to ischemia reperfusion-induced edema in gerbil brains. J Clin Invest 81: 1556–1562

    PubMed  Google Scholar 

  29. Pellegrini-Giampietro DE, Cherici G, Alesiani M, Carla V, Morani F (1988) Exitatory amino acid release from rat hippocampal slices as a consequence of free-radical formation. J Neurochem 51: 1960–1963

    PubMed  Google Scholar 

  30. Petito CK, Pulsinelli WA, Jacobson G, Plum F (1982) Edema and vascular permeability in cerebral ischemia: comparison between ischemic neuronal damage and infarction. J Neuropathol Exp Neurol 41: 423–436

    PubMed  Google Scholar 

  31. Rubanyi GM, Vanhoutte PM (1986) Superoxide anions and hyperoxia inactivate endothelium-derived relaxing factor. Am J Physiol 250: H 822-H 827

    Google Scholar 

  32. Tasdemiroglu E, Christenberry PD, Ardell JL, Chronister RB, Curreri PW, Taylor AE (1989) Ischemia reperfusion injury in the rabbit brain. In: Hoff JT, Betz AL (eds) Intracranial pressure, Vol VII. Springer, Berlin Heidelberg New York Tokyo, pp922–924.

    Google Scholar 

  33. Tasdemiroglu E, Christenberry PD, Ardell JL, Chronister RB, Taylor AE (1993) Effect of Superoxide dismutase on acute reperfusion injury of the rabbit brain. Acta Neurochir (Wien) 120: 180–186

    Google Scholar 

  34. Taylor JJ, Willson RL, Kendall-Taylor P (1984) Evidence for direct interactions between methimazole and free radicals. FEBS Lett 176: 337–340

    Google Scholar 

  35. Weetman AP, Holt ME, Campbell AK, Hall R, McGregor AM (1984) Methimazole and generation of oxygen radicals by monocytes: potential role in immunosuppression. BMJ 288: 518–520

    PubMed  Google Scholar 

  36. Yamamoto K, Yoshimine T, Yanagihara T (1985) Cerebral ischemia in rabbit: a new experimental model with immunohistochemical investigation. J Cereb Blood Flow Metab 5: 529–536

    PubMed  Google Scholar 

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Tasdemiroglu, E., Christenberry, P.D., Ardell, J.L. et al. Effects of antioxidants on the blood-brain barrier and postischemic hyperemia. Acta neurochir 131, 302–309 (1994). https://doi.org/10.1007/BF01808631

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