Arsenic-induced neurotoxicity in relation to toxicokinetics: Effects on sciatic nerve proteins

• Published in: Chemico-biological interactions Vol. 176; no. 2; pp. 188 - 195
• Main Authors: Vahidnia, A., Romijn, F., van der Voet, G.B., de Wolff, F.A.
• Format: Journal Article
• Language: English
• Published: Ireland Elsevier Ireland Ltd 25.11.2008
• Subjects: Animals; Arsenite; Arsenites - pharmacokinetics; Arsenites - toxicity; Arsenites - urine; Body Weight - drug effects; Calpain; Calpain - biosynthesis; Male; Microtubule-associated protein tau; Neurofilament; Neurofilament Proteins - biosynthesis; Neurofilament Proteins - metabolism; Neurotoxicity; Neurotoxins - pharmacokinetics; Neurotoxins - toxicity; Neurotoxins - urine; Peripheral Nervous System - drug effects; Peripheral Nervous System - metabolism; Phosphorylation; Rats; Rats, Wistar; Sciatic Nerve - drug effects; Sciatic Nerve - metabolism; Sodium Compounds - pharmacokinetics; Sodium Compounds - toxicity; Sodium Compounds - urine; Tissue Distribution; Calpain; Neurofilament; Neurotoxicity; Phosphorylation; Arsenite; Microtubule-associated protein tau
• ISSN: 0009-2797; 1872-7786
• DOI: 10.1016/j.cbi.2008.07.001

In our previous study in rats acutely exposed to As, we observed an effect of As on neurofilaments in the sciatic nerve. This study deals with the effects of inorganic As in Wistar rats on the cytoskeletal protein composition of the sciatic nerve after subchronic intoxication. Sodium meta-arsenite (NaAsO 2) dissolved in phosphate-buffered saline (PBS) was administered daily in doses of 0, 3 and 10 mg/kg body weight/day ( n = 9 rats/group) by intragastric route for 4, 8 and 12 week periods. Toxicokinetic measurements revealed a saturation of blood As in the 3- and 10-mg/kg dose groups at approximately 14 μg/ml, with an increase in renal clearance of As at increasing doses. After exsanguination, sciatic nerves were excised and the protein composition was analyzed. Analysis of the sciatic nerves showed compositional changes in their proteins. Protein expression of neurofilament Medium (NF-M) and High (NF-H) was unchanged. Neurofilament protein Low (NF-L) expression was reduced, while μ- and m-calpain protein expression was increased, both in a dose/time pattern. Furthermore, NF-H protein was hypophosphorylated, while NF-L and microtubule-associated protein tau (MAP-tau) proteins were (hyper)-phosphorylated. In conclusion, we show that expression of μ- and m-calpain protein is increased by exposure to As, possibly leading to increased NF-L degradation. In addition, hyperphosphorylation of NF-L and MAP-tau by As also contribute to destabilization and disruption of the cytoskeletal framework, which eventually may lead to axonal degeneration.