Antioxidant activity of the organotellurium compound 3-[4-(N,N-dimethylamino)benzenetellurenyl]propanesulfonic acid against oxidative stress in synaptosomal membrane systems and neuronal cultures

Jaroslaw Kanski, Jennifer Drake, Marina Aksenova, Lars Engman, D. Allan Butterfield

Research output: Contribution to journalArticlepeer-review

45 Scopus citations

Abstract

Antioxidant activities of 3-[4-(N,N-dimethylamino) benzenetellurenyl]propanesulfonic acid sodium salt (NDBT) were evaluated in solution, red blood cells, synaptosomal membranes, and cultured hippocampal neuronal cells after exposure to peroxynitrite (ONOO-) and hydroxyl radicals. The organotellurium compound NDBT possesses significant activity towards hydrogen peroxide and/or the hydroxyl radical in solution, demonstrated by inhibition of hydroxylation of terephthalic acid. In addition, the compound displayed great antioxidant abilities as shown by: reduction of ONOO--induced 2,7-dichlorofluorescein (DCF) fluorescence in synaptosomes; complete prevention of lipid peroxidation in synaptosomes caused by OH radicals (TBARS), and significant prevention of protein oxidation caused by ONOO- and OH, indexed by the levels of protein carbonyls in synaptosomes and neuronal cells. The presence of the compound abolished neuronal cell death caused by ONOO-. Further, the compound was effective in preventing the oxidative changes in synaptosomal membrane protein conformation and crosslinking (EPR spin labeling). Finally, the organotellurium molecule attenuated peroxynitrite-induced, luminol-dependent chemiluminescence in red blood cells - an index of cellular oxidation. These findings demonstrate the great potential of the antioxidant and are consistent with the notion that NDBT may have a role to play in modulating oxidative stress in neurodegenerative disorders, including Alzheimer's disease.

Original languageEnglish
Pages (from-to)12-21
Number of pages10
JournalBrain Research
Volume911
Issue number1
DOIs
StatePublished - Aug 17 2001

Bibliographical note

Funding Information:
The authors would like to acknowledge Dr Sylvia Daunert for use of the luminometer instrument and Dr James W. Geddes for neuronal cell culture assistance. This work was supported in part by the NIH grants to D.A.B. [AG-05119; AG-10836; AG-12423].

Funding

The authors would like to acknowledge Dr Sylvia Daunert for use of the luminometer instrument and Dr James W. Geddes for neuronal cell culture assistance. This work was supported in part by the NIH grants to D.A.B. [AG-05119; AG-10836; AG-12423].

FundersFunder number
National Institutes of Health (NIH)AG-05119, AG-10836
National Institute on AgingR01AG012423

    Keywords

    • Antioxidant
    • Chemiluminescence
    • DCF flourescence
    • EPR
    • Neuronal culture
    • Organotellurium compound
    • Oxidative stress
    • Peroxynitrite
    • Reactive oxygen species
    • Synaptosomal membrane

    ASJC Scopus subject areas

    • General Neuroscience
    • Molecular Biology
    • Clinical Neurology
    • Developmental Biology

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