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Redistribution of glucose-6-phosphate dehydrogenase in response to cerebral ischemia in rat brain

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Abstract

Glucose-6-phosphate dehydrogenase (G6PD), a cytoplasmic enzyme, plays a protective role during oxidative stress in eucaryotic cells, since they provide coenzymes and substrates to the primary antioxidant enzymes. The redistribution of G6PD in the hippocampus was studied post-ischemia (PI). There was a characteristic localisation of G6PD in pyramidal cell layers of the rat hippocampus. In hippocampus CA1 cells were stained weakly whereas CA3 cells showed strong histochemical staining. Ischemia induced up-regulation of G6PD in the hippocampus was in a specific manner. First, the activity increased in the whole hippocampus (at 4 hours PI) which persisted 6 hrs PI in CA1 area. However G6PD activity decreased in the CA3 area & dentate gyrus. At 10 & 24 hrs PI, activity decreased in CA1 area but normalised in CA3 area & dentate gyrus compared to controls. This suggests that the sensitive CA1 neurons are transiently capable of generating an anti-oxidative arsenal to cope with the oxidative stress in the first few hours PI. We can conclude that the brain contains inducible endogenous mechanisms that are capable of enhancing the ability of neurons to withstand lethal ischemic challenge.

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References

  1. Juurlink, B. (1997) Response of glial cells to ischemia: roles of reactive oxygen species and glutathione. Neurosci. Biobehav. Rev. 21, 151–166.

    Article  PubMed  CAS  Google Scholar 

  2. Rosenberg, P. A. and Aizenman, E. (1989) Hundred fold increase in neuronal vulnerability to glutamate toxicity in astrocyte-poor cultures of rat cerebral cortex. Neurosci. Lett. 103(2), 162–168.

    Article  PubMed  CAS  Google Scholar 

  3. Murray, R.K. (1996) Harper's Biochemistry, 24th edn. Prentice-Hall International, Inc., USA p. 794–813.

    Google Scholar 

  4. Rami, A. and Krieglstein, J. (1993) Brain Damage caused by ischemia-pathophysiological and pharmacological aspects. Dementia 4, 21–31.

    Article  PubMed  CAS  Google Scholar 

  5. Sakamoto, A., Ohnishi, S. T., Ohnishi, T. and Ogawa, R. (1991) Relationship between free radical products and rapid lipid peroxidation during ischemia- reperfusion injury in the rat brain. Brain Res. 554(1–2), 186–192.

    Article  PubMed  CAS  Google Scholar 

  6. Schapira, A. H. (1995) Oxidative stress in Parkinson's disease. Neuropathol. Appl. Neurobiol. 21(1), 3–9.

    PubMed  CAS  Google Scholar 

  7. Vanella, A., Di Giacomo, C., Sorrenti, V., Russo, A., Castorina, C., Campisi, A., Renis, M. and Perez-Polo, J. R. (1993) Free radical scavenger depletion in post-ischemic reperfusion brain damage. Neurochem. Res. 18(12), 1337–1340.

    Article  PubMed  CAS  Google Scholar 

  8. Beutler, E., Vulliamy, T. and Luzzatto, L. (1996) Hematologically important mutations: glucose-6-phosphate dehydrogenase. Blood Cells Molecules Dis. 22(1), 49–76.

    Article  CAS  Google Scholar 

  9. Kletzien, R. F., Harris, P. K. and Foellmi, L. A. (1994) Glucose-6-phosphate dehydrogenase: a “housekeeping” enzyme subject to tissue-specific regulation by hormones, nutrients and oxidant stress. FASEB J. 8(2), 174–181.

    PubMed  CAS  Google Scholar 

  10. Cramer, C. T., Cooke, S., Ginsberg, L. C., Kletzien, R. F., Stapleton, S. R. and Ulrich, R. G. (1995) Upregulation of glucose-6-phosphate dehydrogenase in response to hepatocellular oxidative stress: studies with diquat. J. Biochem. Toxicol. 10(6), 293–298.

    Article  PubMed  CAS  Google Scholar 

  11. Salvemini, F., Franze, M., Iervolino, A., Filosa, S., Salzano, S. and Ursini, M.V. (1999) Enhanced glutathione levels of oxidoresistance mediated by increased glucose-6-phosphate dehydrogenase expression. J. Biol. Chem. 274(5), 2750–2757.

    Article  PubMed  CAS  Google Scholar 

  12. Smith, M. L., Bendek, G., Dahgren, N., Rosen, I., Wieloch, T. and Siesjo, B. K. (1984) Models for studying long term recovery following forebrain ischemia in the rat. A2-vessel occlusion model. Acta Neurol. Scand. 69(6), 385–401.

    Article  PubMed  CAS  Google Scholar 

  13. Ninfali, P., Aluigi, G., Balduini, W. and Pompella, A. (1997) Glucose-6-phosphate dehydrogenase activity is higher in the olfactory bulb than in other brain areas, Brain Res. 744(1), 138–142.

    Article  PubMed  CAS  Google Scholar 

  14. Rami, A., Rabie, A. and Winckler, J. (1998) Synergy between Chronic Corticosterone Treatment and Cerebral ischemia in Producing Damage in Noncalbindinergic Neurons. Exp. Neurol. 149, 439–446.

    Article  PubMed  CAS  Google Scholar 

  15. Seif-El-Nasr, M. and El-Fattah, A. A. (1995) Lipid peroxide, phospholipids, glutathione levels and superoxide dismutase activity in rat brain after ischemia: effect of ginko biloba extract. Phamacol. Res. 32(5), 273–278.

    Article  CAS  Google Scholar 

  16. Akai, F., Maeda, M., Suzuki, K., Inagaki, S., Takagi, H. and Tanigushi, N. (1990) Immunocytochemical localisation of manganese superoxide dismutase (Mn-SOD) in the hippocampus of the rat. Neurosci. Lett. 115(1), 19–23.

    Article  PubMed  CAS  Google Scholar 

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(Presently working in Vardhman Mahavir Medical College & Safdarjung Hospital, New Delhi)

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Agarwal, R., Rami, A. Redistribution of glucose-6-phosphate dehydrogenase in response to cerebral ischemia in rat brain. Indian J Clin Biochem 18, 64–70 (2003). https://doi.org/10.1007/BF02867369

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