Cited by 28Glutathione Transferases and PolymorphismsSulfur Compounds in BiologyDrug Transport and Resistance Mechanisms

Formaldehyde induces rapid glutathione export from viable oligodendroglial OLN-93 cells

Tulpule, Ketki, Schmidt, Maike M., Boecker, Karolin, Goldbaum, Olaf, Richter-Landsberg, Christiane, Dringen, Ralf·2012·Neurochemistry International

Abstract

Formaldehyde is a neurotoxic environmental pollutant that can also be produced in the body by certain enzymatic reactions. To test for the potential consequences of an exposure of oligodendrocytes to formaldehyde, we used OLN-93 cells as a model system. Treatment with formaldehyde altered the cellular glutathione (GSH) content of these cells by inducing a rapid time- and concentration-dependent export of GSH. Half-maximal effects were observed for a formaldehyde concentration of about 0.2 mM. While the basal GSH efflux from OLN-93 cells was negligible even when the cellular GSH content was doubled by pre-incubation of the cells with cadmium chloride, the formaldehyde-stimulated export increased almost proportionally to the cellular GSH content. In addition, the stimulated GSH export required the presence of formaldehyde and was almost completely abolished after removal of the aldehyde. Analysis of kinetic parameters of the formaldehyde-induced GSH export revealed similar K(m) and V(max) values of around 100 nmol/mg and 40 nmol/(hmg), respectively, for both OLN-93 cells and cultured astrocytes. The transporter responsible for the formaldehyde-induced GSH export from OLN-93 cells is most likely the multidrug resistance protein 1 (Mrp1), since this transporter is expressed in these cells and since the inhibitor MK571 completely prevented the formaldehyde-induced GSH export. The rapid export of GSH from formaldehyde-treated viable oligodendroglial cells is likely to compromise th…

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Crossref · 10.1016/j.neuint.2012.09.007

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  • The KM-value for GSH export from astrocytes is in the higher millimolar range.

    “While the KM‐value for GSH export from astrocytes is in the higher millimolar range (Arend et al. 2024; Tulpule et al. 2012)”

    From Glutathione Metabolism of the Brain—The Role of Astrocytes (2025) · cites this paper as Tulpule et al. 2012

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Authors
Tulpule, K., Schmidt, M. M., Boecker, K., Goldbaum, O., Richter-Landsberg, C., & Dringen, R.
Affiliations
  • University of Bremen (DE)
  • Carl von Ossietzky Universität Oldenburg (DE)
Corresponding author
Dringen, Ralf
Venue
Neurochemistry International
Publisher
Elsevier BV
Published
2012-12
Volume
61
Issue
8
Pages
1302-1313
ISSN
0197-0186 (ISSN-L)
OpenAlex
W2067484084
Cited by
28
References
2
Citations by year
2025: 4 · 2023: 1 · 2021: 1 · 2020: 2 · 2019: 3 · 2018: 1 · 2017: 1 · 2015: 2 · 2014: 7 · 2013: 6
FWCI
1.93
Type
journal article
Language
en
Open access
closed
Locations
  • Neurochemistry International (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Glutathione Transferases and Polymorphisms
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Sulfur Compounds in Biology
  • Health Sciences › Medicine › Oncology › Drug Transport and Resistance Mechanisms
Keywords
formaldehyde, glutathione export, oligodendrocytes, OLN-93 cells, astrocytes, multidrug resistance protein 1, MRP1, MK571, neurotoxicity, oxidative stress, detoxification, cadmium chloride
MeSH terms
Animals, Astrocytes, Biological Transport, Active, Cell Line, Transformed, Cells, Cultured, Formaldehyde, Glutathione, Nerve Tissue Proteins, Oligodendroglia, Propionates, Quinolines, Rats, Wistar, ATP Binding Cassette Transporter, Subfamily B, Member 1, Rats, Primary Cell Culture

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