In vitro toxicity of Tetrabromobisphenol-A on cerebellar granule cells: cell death, free radical formation, calcium influx and extracellular glutamate
Abstract
Tetrabromobisphenol-A (TBBPA) is one of the worlds most widely used brominated flame retardant. The present study reports effects of TBBPA on primary cultures of cerebellar granule cells (CGC). Using the trypan blue exclusion assay, we show that TBBPA induces death of CGC at low micro molar concentrations. Cell death was reduced by the NMDA receptor antagonist MK-801 (3 microM), the antioxidant vitamin E (50 microM), and in calcium-free buffer. We further demonstrate that TBBPA's toxicity was accompanied by apoptosis-like nuclear shrinkage, chromatin condensation, and DNA fragmentation. Other hallmarks of apoptosis such as caspase activity were, however, absent, indicating an atypical form of apoptosis. TBBPA increased intracellular free calcium in a concentration-dependent manner. TBBPA also induced an increase in extracellular glutamate in a time-dependent manner. TBBPA gave a concentration-dependent increase information reactive oxygen species (ROS) of measured with 2,7-dichlorofluorescein diacetate. The ROS formation was inhibited by the extracellular signal-regulated protein kinase (ERK) inhibitor U0126 (10 microM), the tyrosine kinase inhibitor erbstatin-A (25 microM), eliminating calcium from the buffer and by the superoxide dismutase inhibitor diethyldithio-carbamic acid (DDC, 100 microM). Further analysis with Western blot confirmed phosphorylation of ERK1/2 after exposure to TBBPA. We found that TBBPA induces ROS formation, increases intracellular calcium, extracell…
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TBBPA induces dose-dependent cytotoxicity in cerebellar granule cells, attributed to disturbed calcium currents together with increased oxidative stress.
“TBBPA, for instance, induces dose-dependent cytotoxicity in cerebellar granule cells, an effect attributed to disturbed calcium currents together with increased oxidative stress (Al-Mousa and Michelangeli, 2014; Reistad et al., 2007; Zieminska et al., 2017).”
From Environmental endocrine disruptors at the synapse: mechanisms linking chemical exposure to cognitive and behavioral dysfunction (2026) · cites this paper as Reistad et al., 2007
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Duncia, J. V., Santella, J. B., Higley, C. A., Pitts, W. J., Wityak, J., Frietze, W. E., Rankin, F. W., Sun, J.-H., Earl, R. A., Tabaka, A. C., et al. (1998) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/s0960-894x(98)00522-8 · Cited by 401 · see citing works
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Wojtowicz, A. K., Szychowski, K. A., & Kajta, M. (2014) · Neurotoxicity Research · doi:10.1007/s12640-013-9434-z · Cited by 62 · see citing works
Reistad, T., Fonnum, F., & Mariussen, E. (2013) · Toxicology Letters · doi:10.1016/j.toxlet.2013.01.006 · Cited by 61 · see citing works
Self-citationJocsak, G., Kiss, D. S., Alymbaeva, D., Diebald, A., Zsarnovszky, A., Heinzlmann, A., & Bartha, T. (2026) · Frontiers in Behavioral Neuroscience · doi:10.3389/fnbeh.2026.1821381 · Cited by 1 · see citing works
“TBBPA, for instance, induces dose-dependent cytotoxicity in cerebellar granule cells, an effect attributed to disturbed calcium currents together with increased oxidative stress (Al-Mousa and Michelangeli, 2014; Reistad et al., 2007; Zieminska et al., 2017).”
- Authors
- Reistad, T., Mariussen, E., Ring, A., & Fonnum, F.
- Affiliations
- Norwegian Defence Research Establishment (NO)
- NILU (NO)
- University of Oslo (NO)
- Corresponding author
- Reistad, T.
- ORCID
- Mariussen, E.
- Venue
- Toxicological Sciences
- Publisher
- Oxford University Press (OUP)
- Published
- 2006-10-31
- Volume
- 96
- Issue
- 2
- Pages
- 268-278
- ISSN
- 1096-0929 (ISSN-L)
- 1096-6080
- OpenAlex
- W2153466256
- Cited by
- 125
- References
- 1
- Citations by year
- 2026: 2 · 2025: 2 · 2024: 5 · 2023: 4 · 2022: 7 · 2021: 5 · 2020: 6 · 2019: 8 · 2018: 7 · 2017: 12 · 2016: 10 · 2015: 9 · 2014: 5 · 2013: 9 · 2012: 7
- FWCI
- 4.06
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Toxicological Sciences (publishedVersion)
- PubMed (publishedVersion)
- Funders
- Norges Forskningsråd
- Topics
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Toxic Organic Pollutants Impact
- Physical Sciences › Environmental Science › Health, Toxicology and Mutagenesis › Effects and risks of endocrine disrupting chemicals
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cell death mechanisms and regulation
- Keywords
- tetrabromobisphenol A, brominated flame retardants, cerebellar granule cells, neurotoxicity, apoptosis, reactive oxygen species, intracellular calcium, extracellular glutamate, ERK1/2 phosphorylation, NMDA receptor, vitamin E, caspase-independent cell death, environmental toxins
- MeSH terms
- Animals, Aspartic Acid, Calcium, Cell Nucleus, Cell Survival, Cells, Cultured, Cerebellum, Cytoplasmic Granules, Dose-Response Relationship, Drug, Enzyme Activation, Extracellular Space, Glutamates, Intracellular Fluid, Nucleosomes, Polybrominated Biphenyls, Protein-Tyrosine Kinases, Vitamin E, Hazardous Substances, Dizocilpine Maleate, Cell Death, Reactive Oxygen Species, Okadaic Acid, Caspases, Mitogen-Activated Protein Kinase 3, Rats, DNA Fragmentation, Caspase Inhibitors
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