Skip to main content

Upregulation of NAD(P)H:Quinone Oxidoreductase (NQO1) in Glial Cells of 6-Hydroxydopamine-Lesioned Substantia Nigra in the Rat

  • Conference paper
  • First Online:
The Basal Ganglia IX

Part of the book series: Advances in Behavioral Biology ((ABBI,volume 58))

Abstract

Dopamine quinone toxicity has been implicated in the degeneration of nigral dopaminergic (DA) neurons in Parkinson’s disease (PD). NAD(P)H:quinone oxidoreductase (NQO1) may protect against this quinone toxicity. In Parkinsonian brains, levels of NQO1 are increased in reactive glia cells that are located around the remaining DA neurons in the substantia nigra pars compacta (SNc), suggesting a neuroprotective role of NQO1.

It is not known at which stage of the disease process the upregulation of glial NQO1 starts. Furthermore, it is at present not clear whether NQO1 indeed plays a neuroprotective role in the disease process. As a first step to experimentally study a potential neuroprotective role of NQO1, it was examined whether activation of glia cells and changes in the distribution of NQO1-positive glia cells and the expression levels of glial NQO1, as seen in PD brains, also occurred in a 6-hydroxydopamine (6-OHDA) rat model of PD.

Our results show that astroglia cells and microglia cells were activated. Furthermore, NQO1 was upregulated in astroglia cells in the SNc in those areas in which DA neurons degenerated. The time course and pattern of upregulation of NQO1 paralleled those of the degeneration of DA neurons. Activated microglia were seen at a later stage during the course of degeneration of DA neurons.

In conclusion, in the present model, astroglia cells and microglia cells are activated in response to 6-OHDA-induced oxidative stress. Furthermore, levels of NQO1 are increased in astroglia cells. The findings in the present model are in line with the findings as seen in parkinsonian brains. The 6-OHDA rat model of PD is, therefore, suitable for further research to examine a potential neuroprotective role of NQO1.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 259.00
Price excludes VAT (USA)
  • Available as EPUB and PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 329.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info
Hardcover Book
USD 329.99
Price excludes VAT (USA)
  • Durable hardcover edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

References

  • Bindoli A, Rigobello MP and Deeble DJ (1992) Biochemical and toxicological properties of the oxidation products of catecholamines. Free Radic Biol Med 13: 391–405.

    Article  CAS  PubMed  Google Scholar 

  • Blum D, Torch S, Lambeng N, Nissou M, Benabid AL, Sadoul R and Verna JM (2001) Molecular pathways involved in the neurotoxicity of 6-OHDA, dopamine and MPTP: contribution to the apoptotic theory in Parkinson’s disease. Prog Neurobiol 65: 135–172.

    Article  CAS  PubMed  Google Scholar 

  • Damier P, Hirsch EC, Zhang P, Agid Y and Javoy-Agid F (1993) Glutathione peroxidase, glial cells and Parkinson’s disease. Neuroscience 52: 1–6.

    Article  CAS  PubMed  Google Scholar 

  • Depino AM, Earl C, Kaczmarczyk E, Ferrari C, Besedovsky H, del Rey A, Pitossi FJ and Oertel WH (2003) Microglial activation with atypical proinflammatory cytokine expression in a rat model of Parkinson’s disease. Eur J Neurosci 18: 2731–2742.

    Article  PubMed  Google Scholar 

  • Drukarch B and van Muiswinkel FL (2000) Drug treatment of Parkinson’s disease. Time for phase II. Biochem Pharmacol 59: 1023–1031.

    Article  CAS  PubMed  Google Scholar 

  • Friling RS, Bensimon A, Tichauer Y and Daniel V (1990) Xenobiotic-inducible expression of murine glutathione-S-transferase Ya subunit gene is controlled by an electrophile-responsive element. Proc Natl Acad Sci USA 87: 6258–6262.

    Article  CAS  PubMed  Google Scholar 

  • Hirsch E, Graybiel AM and Agid YA (1988) Melanized dopaminergic neurons are differentially susceptible to degeneration in Parkinson’s disease. Nature 334: 345–348.

    Article  CAS  PubMed  Google Scholar 

  • Hirsch EC (2000) Glial cells and Parkinson’s disease. J Neurol 247 Suppl 2: 1158–1162.

    Google Scholar 

  • Jakel RJ, Kern JT, Johnson DA and Johnson JA (2005) Induction of the protective antioxidant response element pathway by 6-hydroxydopamine in vivo and in vitro. Toxicol Sci 87: 176–186.

    Article  CAS  PubMed  Google Scholar 

  • Kelly VP, Ellis EM, Manson MM, Chanas SA, Moffat GJ, McLeod R, Judah DJ, Neal GE and Hayes JD (2000) Chemoprevention of aflatoxin B1 hepatocarcinogenesis by coumarin, a natural benzopyrone that is a potent inducer of aflatoxin B1-aldehyde reductase, the glutathione S-transferase A5 and P1 subunits, and NAD(P)H:quinone oxidoreductase in rat liver. Cancer Res 60: 957–969.

    CAS  PubMed  Google Scholar 

  • Kohutnicka M, Lewandowska E, Kurkowska-Jastrzebska I, Czlonkowski A and Czlonkowska A (1998) Microglial and astrocytic involvement in a murine model of Parkinson’s disease induced by 1-methyl-4-phenyl-1,2,3,6-tetrahydropyridine (MPTP). Immunopharmacology 39: 167–180.

    Article  CAS  PubMed  Google Scholar 

  • Kreutzberg GW (1996) Microglia: a sensor for pathological events in the CNS. Trends Neurosci 19: 312–318.

    Article  CAS  PubMed  Google Scholar 

  • Murphy TH, So AP and Vincent SR (1998) Histochemical detection of quinone reductase activity in situ using LY 83583 reduction and oxidation. J Neurochem 70: 2156–2164.

    Article  CAS  PubMed  Google Scholar 

  • Napolitano A, Pezzella A and Prota G (1999) New reaction pathways of dopamine under oxidative stress conditions: nonenzymatic iron-assisted conversion to norepinephrine and the neurotoxins 6-hydroxydopamine and 6, 7-dihydroxytetrahydroisoquinoline. Chem Res Toxicol 12: 1090–1097.

    Article  CAS  PubMed  Google Scholar 

  • Nguyen T, Yang CS and Pickett CB (2004) The pathways and molecular mechanisms regulating Nrf2 activation in response to chemical stress. Free Radic Biol Med 37: 433–441.

    Article  CAS  PubMed  Google Scholar 

  • Orr CF, Rowe DB and Halliday GM (2002) An inflammatory review of Parkinson’s disease. Prog Neurobiol 68: 325–340.

    Article  CAS  PubMed  Google Scholar 

  • Paxinos G and Watson C (1998) The Rat Brain in Stereotaxic Coordinates, New York: Academic Press

    Google Scholar 

  • Rushmore TH and Pickett CB (1990a) Transcriptional regulation of the rat glutathione S-transferase Ya subunit gene. Characterization of a xenobiotic-responsive element controlling inducible expression by phenolic antioxidants. J Biol Chem 265: 14648–14653.

    CAS  PubMed  Google Scholar 

  • Rushmore TH, King RG, Paulson KE and Pickett CB (1990b) Regulation of glutathione S-transferase Ya subunit gene expression: identification of a unique xenobiotic-responsive element controlling inducible expression by planar aromatic compounds. Proc Natl Acad Sci USA 87: 3826–3830.

    Article  CAS  PubMed  Google Scholar 

  • Rushmore TH, Morton MR and Pickett CB (1991a) The antioxidant responsive element. Activation by oxidative stress and identification of the DNA consensus sequence required for functional activity. J Biol Chem 266: 11632–11639.

    CAS  PubMed  Google Scholar 

  • Rushmore TH and Pickett CB (1991b) Xenobiotic responsive elements controlling inducible expression by planar aromatic compounds and phenolic antioxidants. Methods Enzymol 206: 409–420.

    Article  CAS  PubMed  Google Scholar 

  • Schmued LC and Hopkins KJ (2000) Fluoro-Jade B: a high affinity fluorescent marker for the localization of neuronal degeneration. Brain Res 874: 123–130.

    Article  CAS  PubMed  Google Scholar 

  • Smythies J and Galzigna L (1998) The oxidative metabolism of catecholamines in the brain: a review. Biochim Biophys Acta 1380: 159–162.

    CAS  PubMed  Google Scholar 

  • Spencer JP, Jenner P, Daniel SE, Lees AJ, Marsden DC and Halliwell B (1998) Conjugates of catecholamines with cysteine and GSH in Parkinson’s disease: possible mechanisms of formation involving reactive oxygen species. J Neurochem 71: 2112–2122.

    Article  CAS  PubMed  Google Scholar 

  • Stokes AH, Hastings TG and Vrana KE (1999) Cytotoxic and genotoxic potential of dopamine. J Neurosci Res 55: 659–665.

    Article  CAS  PubMed  Google Scholar 

  • Teismann P and Schulz JB (2004) Cellular pathology of Parkinson’s disease: astrocytes, microglia and inflammation. Cell Tissue Res 318: 149–161.

    Article  PubMed  Google Scholar 

  • Tsuchida M, Miura T and Aibara K (1987) Lipofuscin and lipofuscin-like substances. Chem Phys Lipids 44: 297–325.

    Article  CAS  PubMed  Google Scholar 

  • van Muiswinkel FL, de Vos RA, Bol JG, Andringa G, Jansen Steur EN, Ross D, Siegel D and Drukarch B (2004) Expression of NAD(P)H:quinone oxidoreductase in the normal and Parkinsonian substantia nigra. Neurobiol Aging 25: 1253–1262.

    Article  PubMed  Google Scholar 

  • Zhang P, Anglade P, Hirsch EC, Javoy-Agid F and Agid Y (1994) Distribution of manganese-dependent superoxide dismutase in the human brain. Neuroscience 61: 317–330.

    Article  CAS  PubMed  Google Scholar 

  • Zuch CL, Nordstroem VK, Briedrick LA, Hoernig GR, Granholm AC and Bickford PC (2000) Time course of degenerative alterations in nigral dopaminergic neurons following a 6-hydroxydopamine lesion. J Comp Neurol 427: 440–454.

    Article  CAS  PubMed  Google Scholar 

Download references

Acknowledgments

The excellent drawing skills of Mr. Dirk de Jong in preparing the figures are gratefully acknowledged.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Pieter Voorn .

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 2009 Springer Science+Business Media, LLC

About this paper

Cite this paper

Kil, A.C., Drukarch, B., Jonker, A.J., Groenewegen, H.J., Voorn, P. (2009). Upregulation of NAD(P)H:Quinone Oxidoreductase (NQO1) in Glial Cells of 6-Hydroxydopamine-Lesioned Substantia Nigra in the Rat. In: Groenewegen, H., Voorn, P., Berendse, H., Mulder, A., Cools, A. (eds) The Basal Ganglia IX. Advances in Behavioral Biology, vol 58. Springer, New York, NY. https://doi.org/10.1007/978-1-4419-0340-2_32

Download citation

  • DOI: https://doi.org/10.1007/978-1-4419-0340-2_32

  • Published:

  • Publisher Name: Springer, New York, NY

  • Print ISBN: 978-1-4419-0339-6

  • Online ISBN: 978-1-4419-0340-2

  • eBook Packages: MedicineMedicine (R0)

Publish with us

Policies and ethics