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Glutathione depletion in rat brain does not cause nigrostriatal pathway degeneration

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Summary

Nigral cell death in Parkinson's disease (PD) may involve oxidative stress and mitochondrial dysfunction initiated by a decrease in reduced glutathione (GSH) levels in substantia nigra. L-buthionine-(S,R)-sulphoximine (BSO; 4.8 and 9.6 mg/kg/day), an irreversible inhibitor of γ-glutamyl cysteine synthetase, was chronically infused into the left lateral ventricle of rats over a period of 28 days and markedly reduced GSH concentrations in substantia nigra (approx. 59% and 65% in 4.8 and 9.6 mg/kg/d BSO respectively) and the striatum (approx. 63% and 80% in 4.8 and 9.6 mg/kg/d BSO respectively). However, the number of tyrosine hydroxylase (TH)-positive cells in substantia nigra was not altered by BSO-treatment compared to control animals. Similarly, there was no difference in specific [3H]-mazindol binding in the striatum and nucleus accumbens of BSO-treated rats compared to control rats. In conclusion, depletion of GSH following chronic administration of BSO in the rat brain does not cause damage to the nigrostriatal pathway and suggests that loss of GSH alone is not responsible for nigrostriatal damage in PD. Rather, GSH depletion may enhance the susceptibility of substantia nigra to destruction by endogenous or exogenous toxins.

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References

  • Dexter DT, Sian J, Jenner P, Marsden CD (1993) Implications of alterations in trace elements in Parkinson's disease and other neurological disorders affecting the basal ganglia. Adv Neurol 60: 273–281

    PubMed  Google Scholar 

  • Dexter DT, Sian J, Rose S, Hindmarsh JG, Mann VM, Cooper JM, Wells FR, Daniel SE, Lees AJ, Schapira AHV, Jenner P, Marsden CD (1994) Indices of oxidative stress and mitochondrial function in individuals with incidental Lewy body disease. Ann Neurol 35: 38–44

    PubMed  Google Scholar 

  • Gibb WRG, Lees AJ (1988) The relevence of Lewy body to the pathogenesis of idiopathic Parkinson's disease. J Neurol Neurosurg Psychiatry 51: 745–752

    PubMed  Google Scholar 

  • Griffith OW (1982) Mechanism of action, metabolism and toxicity of buthionine sulphoximine and its higher homologues, potent inhibitors of glutathione synthesis. J Biol Chem 257: 13704–13712

    PubMed  Google Scholar 

  • Griffith OW, Meister A (1985) Origin and turnover of mitochondrial glutathione. PNAS 82: 4668–4672

    PubMed  Google Scholar 

  • Jain A, Martensson J, Stole E, Auld PA, Meister A (1991) Glutathione deficiency leads to mitochondrial damage in brain. PNAS 88: 1913–1917

    PubMed  Google Scholar 

  • Javitch JA, Strittmatter SM, Snyder SH (1985) Differential visualisation of dopamine and norepinephrine uptake sites in rat brain using [3H]-mazindol autoradiography. J Neurosci 5: 1513–1521

    PubMed  Google Scholar 

  • Jellinger K (1987) The pathology of parkinsonism, 1st edn. Movement disorders 2. Butterworths, London, pp 125–130

    Google Scholar 

  • Jenner P, Schapira AHV, Marsden CD (1992) New insights into the cause of Parkinson's disease. Neurology 42: 2241–2250

    PubMed  Google Scholar 

  • Mann VM, Cooper JM, Daniel SE, Srai K, Jenner P, Marsden CD, Schapira AHV (1994) Complex I, iron, and ferritin in Parkinson's disease substantia nigra. Ann Neurol 3: 876–881

    Google Scholar 

  • Meister A (1991) Glutathione deficiency produced by inhibition of its synthesis and its reversal: applications in research and therapy. Pharmacol Ther 51: 155–194

    PubMed  Google Scholar 

  • Paxinos G, Watson C (1986) The rat brain in stereotaxic co-ordinates, 2nd edn. Academic Press, San Diego

    Google Scholar 

  • Pellegrino LJ, Pellegrino AS, Cushman AJ (1979) Stereotaxic atlas of the rat brain, 2nd edn. Plenum Press, New York

    Google Scholar 

  • Perry TL, Godin DV, Hansen S (1982) Parkinson's disease: a disorder due to nigral glutathione deficiency? Neurosci Lett 33: 305–310

    PubMed  Google Scholar 

  • Pileblad E, Magnusson T (1989) Intracerebrovetricular administration of L-buthionine sulfoximine: a method for depleting brain glutathione. J Neurochem 53: 1878–1882

    PubMed  Google Scholar 

  • Pileblad E, Magnusson T, Fornstedt B (1989) Reduction of brain glutathione by L-buthionine sulfoximine potentiates the dopamine-depleting action of 6-hydroxydopamine in rat striatum. J Neurochem 52: 978–980

    PubMed  Google Scholar 

  • Reed DJ, Babson JR, Beatty PW, Brodie AE, Ellis WW, Potter DW (1980) High performance liquid chromatography analysis of nanomole levels of glutathione, glutathione disulphide, and related thiols and disulphides. Anal Biochem 106: 55–62

    PubMed  Google Scholar 

  • Riederer P, Sofic E, Rausch W, Schmidt B, Reynolds GP, Jellinger K, Youdim MBH (1988) Transition metals, ferritin, glutathione and ascorbic acid in parkinsonian brains. J Neurochem 52: 515–520

    Google Scholar 

  • Schapira AHV (1994) Evidence for mitochondrial dysfunction in Parkinson's disease: a critical appraisal. Mov Disord 9: 125–138

    PubMed  Google Scholar 

  • Seaton TA, Jenner P, Marsden CD (1996) Thioctic acid does not restore glutathione levels or protect against the potentiation of 6-hydroxydopamine toxicity induced by glutathione depletion in rat brain. J Neural Transm 103: 315–329

    PubMed  Google Scholar 

  • Sian J, Dexter DT, Lees AJ, Daniel S, Agid Y, Javoy-Agid F, Jenner P, Marsden CD (1994a) Alterations in glutathione levels in Parkinson's disease and other neurodegenerative disorders affecting basal ganglia. Ann Neurol 36: 348–355

    PubMed  Google Scholar 

  • Sian J, Dexter DT, Lees AJ, Daniel S, Jenner P, Marsden CD (1994b) Glutathionerelated enzymes in Parkinson's disease. Ann Neurol 36: 356–361

    PubMed  Google Scholar 

  • Sofic E, Paulus W, Jellinger P, Riederer P, Youdim MBH (1991) Selective increase of iron in substantia nigra zona compacta of parkinsonian brains. J Neurochem 56: 978–982

    PubMed  Google Scholar 

  • Wüllner U, Löschmann P-A, Eblen F, Klockgether (1995) Glutathione depletion potentiates MPP+ toxicity. J Neurol [Suppl 2] 242: 571

    Google Scholar 

  • Wüllner U, Löschmann P-A, Schulz JB, Schmid A, Dringen R, Eblen F, Turksi L, Klockgether T (1996) Glutathione depletion potentiates MPTP and MPP+ toxicity in nigral dopaminergic neurones. NeuroReport 7: 921–923

    PubMed  Google Scholar 

  • Youdim MBH, Ben Schahar D, Riederer P (1989) Is Parkinson's disease a progressive siderosis of substantia nigra resulting in increased iron and melanin induced neurodegeneration? Acta Neurol Scand 126: 47–54

    Google Scholar 

  • Zarow C, Chui HC (1991) A simple method for assessing neuronal number in the human substantia nigra. Soc Neurosci Abstr 17: 574.10

    Google Scholar 

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Toffa, S., Kunikowska, G.M., Zeng, B.Y. et al. Glutathione depletion in rat brain does not cause nigrostriatal pathway degeneration. J. Neural Transmission 104, 67–75 (1997). https://doi.org/10.1007/BF01271295

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  • DOI: https://doi.org/10.1007/BF01271295

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