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Cytochrome oxidase activity during acute focal ischaemia in rat brain

A pathophysiology of acute focal ischaemia: Part 2

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Summary

An enzyme-histochemical technique was used to examine the changes in cytochrome oxidase activity during acute focal ischaemia in the rat. In the somatosensory cortex, the enzyme activity began to increase significantly (p < 0.01) 1 hour after middle cerebral artery occlusion (MCAO) and continued to increase up to 3 hours, during which ischaemic cell damage was not detected. In the striatum, the enzyme activity increased significantly (p < 0.01) 1 hour after MCAO in the absence of morphological evidence of ischaemic cell damage; a peak activity was reached at 2 hours, and began to decline 3 hours after MCAO when moderate ischaemic change was detected. In both cortical and subcortical areas, the enzyme activity tended to decrease from 4 hours after MCAO, and was reduced to a level similar to or below that of the non-ischaemic hemisphere 5 hours after MCAO, when severe ischaemic damage was demonstrated. The relation of this transient increase of cytochrome oxidase activity in the early stage of acute ischaemia and the hypermetabolism of neuronal cells during ischaemic insult was discussed.

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References

  1. Aoki C, Milner TA, Berger SB, Sheu KFR, Blass JP, Pickel VM (1987) Glial glutamate dehydrogenase: ultrastructural localization and regional distribution in relation to the mitochondrial enzyme, cytochrome oxidase. J Neurosci Res 18: 305–318

    PubMed  Google Scholar 

  2. Clark JB, Nicklas WJ (1970) The metabolism of rat brain mitochondria. Preparation and characterization. J Biol Chem 245: 4724–4731

    PubMed  Google Scholar 

  3. Dagani F, Marzatico F, Curti D, Zanada F, Benzi G (1984) Effect of prolonged and intermittent hypoxia on some cerebral enzymatic activities related to energy transduction. J Cereb Blood Flow Metab 4: 615–624

    PubMed  Google Scholar 

  4. Darriet D, Der T, Collins RC (1986) Distribution of cytochrome oxidase in rat brain studies with diaminobenzidine histochemistry in vitro and [14C] cyanide tissue labelling in vivo. J Cereb Blood Flow Metab 6: 8–14

    PubMed  Google Scholar 

  5. Dimlich RVW, Showers MJ, Shipley MT (1990) Densitometric analysis of cytochrome oxidase in ischemie rat brain. Brain Res 516: 181–191

    PubMed  Google Scholar 

  6. Duckrow RB, LaManna JC, Rosenthal M (1981) Direct electrical stimulation of the cerebral cortex suggests that vascular as well as metabolic factors determine the oxidative response. Neuroscience Abs 7: 787

    Google Scholar 

  7. Farooqui AA, Horrocks LA (1991) Excitatory amino acid receptors, neural membrane phospholipid metabolism and neurological disorders. Brain Res Rev 16: 171–191

    PubMed  Google Scholar 

  8. Fridovich I, Handler P, Xanthine oxidase (1962) V. Differential inhibition of the reduction of various electron acceptors. J Biol Chem 237: 916–920

    PubMed  Google Scholar 

  9. Ginsberg MD, Mela L, Wrobel-Kuhl W, Reivich M (1977) Mitochondrial metabolism following bilateral cerebral ischemia in the gerbil. Ann Neurol 1: 519–527

    PubMed  Google Scholar 

  10. Hamberger A, Hyden H (1963) Inverse enzymatic changes in neurons and glia during increased function and hypoxia. J Biol Chem 16: 521–525

    Google Scholar 

  11. Hillered L (1986) Mechanisms of mitochondrial damage in brain ischemia. In: Fiskum G (ed.), Mitochondrial physiology and pathology. Van Nostrand Reinhold, New York, pp 120–146

    Google Scholar 

  12. Kageyama GH, Wong-Riley MTT (1982) Histochemical localization of cytochrome oxidase in the hippocampus: correlation with specific neuronal types and afferent pathways. Neuroscience 7: 2337–2361

    PubMed  Google Scholar 

  13. McCord JM, Fridovich I (1986) The reduction of cytochrome C by milk xanthine oxidase. J Biol Chem 243: 5753–5760

    Google Scholar 

  14. Nakahara I, Kikuchi H, Taki W, Nishi S, Kito M, Yonekawa Y, Goto Y, Ogata N (1991) Degradation of mitochondrial phospholipids during experimental cerebral ischemia in rats. J Neurochem 57: 839–844

    PubMed  Google Scholar 

  15. Ozawa K, Seta K, Araki H, Handa H (1967) The effect of ischemia on mitochondrial metabolism. J Biochem 61: 512–514

    PubMed  Google Scholar 

  16. Rehncrona S, Mela L, Siesjo BK (1979) Recovery of brain mitochondrial function in the rat after complete and incomplete cerebral ischemia. Stroke 10: 437–446

    PubMed  Google Scholar 

  17. Ribak CE (1981) The histochemical localization of cytochrome oxidase in the dentate gyrus of the rat hippocampus. Brain Res 212: 169–174

    PubMed  Google Scholar 

  18. Siesjo BK (1981) Cell damage in the brain a speculative synthase. J Cereb Blood Flow Metab 1: 155–185

    PubMed  Google Scholar 

  19. Siesjo BK (1984) Cerebral circulation and metabolism. J Neurosurg 60: 883–908

    PubMed  Google Scholar 

  20. Siesjo BK, Agardh CD, Bengtsson F (1989) Free radicals and brain damage. Cerebrovasc Brain Metab Rev 1: 165–211

    PubMed  Google Scholar 

  21. Smialek M, Hamberger A (1970) The effect of moderate hypoxia and ischemia on cytochrome oxidase activity and protein synthesis in brain mitochondria. Brain Res 17: 369–371

    PubMed  Google Scholar 

  22. Takeuchi Y, Morii H, Tamura M, Hayashi O, Watanabe Y (1991) A possible mechanism of mitochondrial dysfunction during cerebral ischemia: inhibition of mitochondrial respiration activity by arachidonic acid. Arch Biochem Biophys 289: 3–38

    Google Scholar 

  23. Tamura A, Graham DI, McCulloch J, Teasdale GM (1981) Focal cerebral ischemia in the rat: 1. Description of technique and early neurological consequences following middle cerebral artery occlusion. J Cereb Blood Flow Metab 1: 53–60

    PubMed  Google Scholar 

  24. Vandeplassche G, Hermans C, Thone F, Borgers M (1991) Stunned myocardium has increased mitochondrial NADH oxidase and ATP ase activities. Cardioscience 2: 47–53

    PubMed  Google Scholar 

  25. Wagner KR, Kleinholz M, Myers E (1990) Delayed onset of neurologic deterioration following anoxia/ischemia coincides with appearance of impaired brain mitochondrial respiration and decreased cytochrome oxidase activity. J Cereb Blood Flow Metab 10: 417–423

    PubMed  Google Scholar 

  26. Wong-Riley MTT (1976) Endogenous peroxidatic activity in brain stem neurons as demonstrated by their staining with diaminobenzidine in normal squirrel monkeys. Brain Res 108: 257–277

    PubMed  Google Scholar 

  27. Wong-Riley MTT, Merzenich MM, Leak PA (1978) Changes in endogeneous enzymatic reactivity to DAB induced by neuronal inactivity. Brain Res 141: 185–192

    PubMed  Google Scholar 

  28. Wong-Riley MTT (1978) Changes in the visual system of monocularly sutured or enucleated cats demonstrable with the cytochrome oxidase technique. Anat Rec 190: 586

    Google Scholar 

  29. Wong-Riley MTT (1979) Changes in the visual system of monocularly sutured or enucleated cats demonstrable with cytochrome oxidase histochemistry. Brain Res 171: 11–28

    Article  Google Scholar 

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Inoue, N., Goto, S., Korematsu, K. et al. Cytochrome oxidase activity during acute focal ischaemia in rat brain. Acta neurochir 138, 1126–1131 (1996). https://doi.org/10.1007/BF01412318

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