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Mercury Induces Cell Cytotoxicity and Oxidative Stress and Increases β‐Amyloid Secretion and Tau Phosphorylation in SHSY5Y Neuroblastoma Cells
Author(s) -
Olivieri G.,
Brack Ch.,
MüllerSpahn F.,
Stähelin H. B.,
Herrmann M.,
Renard P.,
Brockhaus M.,
Hock C.
Publication year - 2000
Publication title -
journal of neurochemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.75
H-Index - 229
eISSN - 1471-4159
pISSN - 0022-3042
DOI - 10.1046/j.1471-4159.2000.0740231.x
Subject(s) - melatonin , cytotoxicity , glutathione , oxidative stress , neuroblastoma , chemistry , mtt assay , cell culture , neurotoxicity , amyloid beta , endocrinology , medicine , microbiology and biotechnology , toxicity , cell growth , biochemistry , in vitro , biology , peptide , enzyme , genetics , organic chemistry
Abstract: Concentrations of heavy metals, including mercury, have been shown to be altered in the brain and body fluids of Alzheimer’s disease (AD) patients. To explore potential pathophysiological mechanisms we used an in vitro model system (SHSY5Y neuroblastoma cells) and investigated the effects of inorganic mercury (HgCl 2 ) on oxidative stress, cell cytotoxicity, β‐amyloid production, and tau phosphorylation. We demonstrated that exposure of cells to 50 μg/L (180 n M ) HgCl 2 for 30 min induces a 30% reduction in cellular glutathione (GSH) levels (n = 13, p < 0.001). Preincubation of cells for 30 min with 1 μ M melatonin or premixing melatonin and HgCl 2 appeared to protect cells from the mercury‐induced GSH loss. Similarly, 3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide (MTT) cytotoxicity assays revealed that 50 μg/L HgCl 2 for 24 h produced a 50% inhibition of MTT reduction (n = 9, p < 0.001). Again, melatonin preincubation protected cells from the deleterious effects of mercury, resulting in MTT reduction equaling control levels. The release of β‐amyloid peptide (Aβ) 1‐40 and 1‐42 into cell culture supernatants after exposure to HgCl 2 was shown to be different: Aβ 1‐40 showed maximal (15.3 ng/ml) release after 4 h, whereas Aβ 1‐42 showed maximal (9.3 ng/ml) release after 6 h of exposure to mercury compared with untreated controls (n = 9, p < 0.001). Preincubation of cells with melatonin resulted in an attenuation of Aβ 1‐40 and Aβ 1‐42 release. Tau phosphorylation was significantly increased in the presence of mercury (n = 9, p < 0.001), whereas melatonin preincubation reduced the phosphorylation to control values. These results indicate that mercury may play a role in pathophysiological mechanisms of AD.