Literature DB >> 1908956

Oxygen toxicity in the nervous tissue: comparison of the antioxidant defense of rat brain and sciatic nerve.

F J Romero1, E Monsalve, C Hermenegildo, F J Puertas, V Higueras, E Nies, J Segura-Aguilar, J Romá.   

Abstract

Nervous tissue, central and peripheral, is, as any other, subject to variations in oxygen tension, and to the attack of different xenobiotics; these situations may promote the generation of activated oxygen species of free radical character. Results are presented showing that the content of total glutathione (GSH) in brain is 10-fold that found in the sciatic nerve of the rat (2620 vs. 261 nmol/g wet weight, respectively). The existence of a relatively high superoxide dismutase activity in peripheral nervous tissue, when compared with brain or liver, in combination with the DT-diaphorase activity detected in the sciatic nerve might represent an effective defense mechanism against quinone toxicity, as is also discussed. Nervous tissue, both central and peripheral lack Se-independent GSH peroxidase activity. Finally, the activities of other glutathione-related enzymes studied in the sciatic nerve are very low, when compared with the central nervous tissue, thus suggesting a higher susceptibility of peripheral tissue to oxidative stress damage, since GSH concentration and/or any GSH-related enzymatic activities, e.g. GSH peroxidase or glutathione disulfide reductase, might become limiting.

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Year:  1991        PMID: 1908956     DOI: 10.1007/bf00965704

Source DB:  PubMed          Journal:  Neurochem Res        ISSN: 0364-3190            Impact factor:   3.996


  32 in total

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Authors:  D Jamieson; B Chance; E Cadenas; A Boveris
Journal:  Annu Rev Physiol       Date:  1986       Impact factor: 19.318

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Journal:  FEBS Lett       Date:  1986-07-28       Impact factor: 4.124

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Journal:  Comp Biochem Physiol C       Date:  1981

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Authors:  U Reiss; D Gershon
Journal:  Biochem Biophys Res Commun       Date:  1976-11-22       Impact factor: 3.575

5.  Metabolism of benzo(a)pyrene-3,6-quinone and 3-hydroxybenzo(a)pyrene in liver microsomes from 3-methylcholanthrene-treated rats. A possible role of DT-diaphorase in the formation of glucuronyl conjugates.

Authors:  C Lind; H Vadi; L Ernster
Journal:  Arch Biochem Biophys       Date:  1978-09       Impact factor: 4.013

6.  On the mechanism of the Mn3(+)-induced neurotoxicity of dopamine:prevention of quinone-derived oxygen toxicity by DT diaphorase and superoxide dismutase.

Authors:  J Segura-Aguilar; C Lind
Journal:  Chem Biol Interact       Date:  1989       Impact factor: 5.192

Review 7.  Careful consideration of the effects induced by glutathione depletion in rat liver and heart. The involvement of cytosolic and mitochondrial glutathione pools.

Authors:  F J Romero; J Romá
Journal:  Chem Biol Interact       Date:  1989       Impact factor: 5.192

8.  Reversible inactivation of Saccharomyces cerevisiae glutathione reductase under reducing conditions.

Authors:  M C Pinto; A M Mata; J Lopez-Barea
Journal:  Arch Biochem Biophys       Date:  1984-01       Impact factor: 4.013

9.  Structure-activity relationships of 4-hydroxyalkenals in the conjugation catalysed by mammalian glutathione transferases.

Authors:  U H Danielson; H Esterbauer; B Mannervik
Journal:  Biochem J       Date:  1987-11-01       Impact factor: 3.857

10.  Dopamine sulfoconjugation in the rat brain: regulation by monoamine oxidase.

Authors:  N T Buu
Journal:  J Neurochem       Date:  1985-08       Impact factor: 5.372

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  11 in total

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3.  Postnatal expression of glucose-6-phosphate dehydrogenase in different brain areas.

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4.  Management of oxidative stress in the CNS: the many roles of glutathione.

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5.  The heme precursor delta-aminolevulinate blocks peripheral myelin formation.

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6.  Stereological analysis of sciatic nerve in chickens following neonatal pinealectomy: an experimental study.

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7.  Decreased glutathione peroxidase activity in sciatic nerve of alloxan-induced diabetic mice and its correlation with blood glucose levels.

Authors:  C Hermenegildo; A Raya; J Romá; F J Romero
Journal:  Neurochem Res       Date:  1993-08       Impact factor: 3.996

Review 8.  Glucose-6-phosphate dehydrogenase expression associated with NADPH-dependent reactions in cerebellar neurons.

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Journal:  Cerebellum       Date:  2003       Impact factor: 3.847

9.  Oxidative stress induced by loss of Cu,Zn-superoxide dismutase (SOD1) or superoxide-generating herbicides causes axonal degeneration in mouse DRG cultures.

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Review 10.  New treatments for diabetic neuropathy: pathogenetically oriented treatment.

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