Int. J. Environ. Res. Public Health 2011, 8(1), 203-221; doi:10.3390/ijerph8010203
Article

Toxicity of Neurons Treated with Herbicides and Neuroprotection by Mitochondria-Targeted Antioxidant SS31

1email, 1email, 1email, 1email, 1email, 1email, 2email and 1,3,* email
Received: 31 December 2010; in revised form: 13 January 2011 / Accepted: 17 January 2011 / Published: 19 January 2011
(This article belongs to the Special Issue Advances in Environmental Neurotoxicology)
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Abstract: The purpose of this study was to determine the neurotoxicity of two commonly used herbicides: picloram and triclopyr and the neuroprotective effects of the mitochondria-targeted antioxidant, SS31. Using mouse neuroblastoma (N2a) cells and primary neurons from C57BL/6 mice, we investigated the toxicity of these herbicides, and protective effects of SS1 peptide against picloram and triclopyr toxicity. We measured total RNA content, cell viability and mRNA expression of peroxiredoxins, neuroprotective genes, mitochondrial- encoded electron transport chain (ETC) genes in N2a cells treated with herbicides and SS31. Using primary neurons from C57BL/6 mice, neuronal survival was studied in neurons treated with herbicides, in neurons pretreated with SS31 plus treated with herbicides, neurons treated with SS31 alone, and untreated neurons. Significantly decreased total RNA content, and cell viability in N2a cells treated with picloram and triclopyr were found compared to untreated N2a cells. Decreased mRNA expression of neuroprotective genes, and ETC genes in cells treated with herbicides was found compared to untreated cells. Decreased mRNA expression of peroxiredoxins 1–6 in N2a cells treated with picloram was found, suggesting that picloram affects the antioxidant enzymes in N2a cells. Immunofluorescence analysis of primary neurons revealed that decreased neuronal branching and degenerating neurons in neurons treated with picloram and triclopyr. However, neurons pretreated with SS31 prevented degenerative process caused by herbicides. Based on these results, we propose that herbicides—picloram and triclopyr appear to damage neurons, and the SS31 peptide appears to protect neurons from herbicide toxicity.
Keywords: Mitochondria-targeted antioxidant; herbicides; Picloram; Triclopyr; Szeto-Schiller peptide 31; mouse neuroblastoma cells; mouse primary hippocampal neurons; electron transport chain; oxidative stress
PDF Full-text Download PDF Full-Text [562 KB, uploaded 19 June 2014 02:45 CEST]

Export to BibTeX |
EndNote


MDPI and ACS Style

Reddy, T.P.; Manczak, M.; Calkins, M.J.; Mao, P.; Reddy, A.P.; Shirendeb, U.; Park, B.; Reddy, P.H. Toxicity of Neurons Treated with Herbicides and Neuroprotection by Mitochondria-Targeted Antioxidant SS31. Int. J. Environ. Res. Public Health 2011, 8, 203-221.

AMA Style

Reddy TP, Manczak M, Calkins MJ, Mao P, Reddy AP, Shirendeb U, Park B, Reddy PH. Toxicity of Neurons Treated with Herbicides and Neuroprotection by Mitochondria-Targeted Antioxidant SS31. International Journal of Environmental Research and Public Health. 2011; 8(1):203-221.

Chicago/Turabian Style

Reddy, Tejaswini P.; Manczak, Maria; Calkins, Marcus J.; Mao, Peizhong; Reddy, Arubala P.; Shirendeb, Ulziibat; Park, Byung; Reddy, P. Hemachandra. 2011. "Toxicity of Neurons Treated with Herbicides and Neuroprotection by Mitochondria-Targeted Antioxidant SS31." Int. J. Environ. Res. Public Health 8, no. 1: 203-221.

Int. J. Environ. Res. Public Health EISSN 1660-4601 Published by MDPI AG, Basel, Switzerland RSS E-Mail Table of Contents Alert