TY - JOUR
T1 - Protective effects of novel organic selenium compounds against oxidative stress in the nematode Caenorhabditis elegans
AU - Stefanello, Sílvio Terra
AU - Gubert, Priscila
AU - Puntel, Bruna
AU - Mizdal, Caren Rigon
AU - de Campos, Marli Matiko Anraku
AU - Salman, Syed M.
AU - Dornelles, Luciano
AU - Avila, Daiana Silva
AU - Aschner, Michael
AU - Soares, Félix Alexandre Antunes
N1 - Funding Information:
This work was carried out with funds from Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq Universal #472669/2011-7 and #475896/2012-2), Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES for providing fellowship to S.T.S. and P.G.) and Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul (Programa de Apoio a Núcleos emergentes - PRONEM/FAPERGS #11/2029-1, for providing fellowship to B.P.). Prof. Michael Aschner was supported in part by grants from the National Institute of Environmental Health Sciences (NIEHS) R01 ES10563 and R01 ES 07731.
Publisher Copyright:
© 2015.
PY - 2015/7/6
Y1 - 2015/7/6
N2 - Organic selenium compounds possess numerous biological properties, including antioxidant activity. Yet, the high toxicity of some of them, such as diphenyl diselenide (DPDS), is a limiting factor in their current usage. Accordingly, we tested four novel organic selenium compounds in the non-parasite nematode Caenorhabditis elegans and compared their efficacy to DPDS. The novel organic selenium compounds are β-selenoamines 1-phenyl-3-(p-tolylselanyl)propan-2-amine (C1) and 1-(2-methoxyphenylselanyl)-3-phenylpropan-2-amine (C2) and analogs of DPDS 1,2-bis(2-methoxyphenyl)diselenide (C3) and 1,2-bis. p-tolyldiselenide (C4). Synchronized worms at the L4 larval stage were exposed for one hour in M9 buffer to these compounds. Oxidative stress conditions were induced by juglone (200. μM) and heat shock (35. °C). Moreover, we evaluated C. elegans behavior, GST-4::GFP (glutathione S-transferase) expression and the activity of acetylcholinesterase (AChE). All tested compounds efficiently restored viability in juglone stressed worms. However, DPDS, C2, C3 and C4 significantly decreased the defecation cycle time. Juglone-induced GST-4::GFP expression was not attenuated in worms pretreated with the novel compounds, except with C2. Finally, AChE activity was reduced by DPDS, C2, C3 and C4. To our knowledge, this is study firstly showed the effects of C1, C2, C3 and C4 selenium-derived compounds in C. elegans. Low toxic effects were noted, except for reduction in the defecation cycle, which is likely associated with AChE inhibition. The juglone-induced stress (reduced viability) was fully reversed by compounds to control animal levels. C2 was also efficient in reducing the juglone-induced GST-4::GFP expression, suggesting the latter may mediate the stress induced by this compound. Future studies could be profitably directed at addressing additional molecular mechanisms that mediate the protective effects of these novel organic selenium compounds.
AB - Organic selenium compounds possess numerous biological properties, including antioxidant activity. Yet, the high toxicity of some of them, such as diphenyl diselenide (DPDS), is a limiting factor in their current usage. Accordingly, we tested four novel organic selenium compounds in the non-parasite nematode Caenorhabditis elegans and compared their efficacy to DPDS. The novel organic selenium compounds are β-selenoamines 1-phenyl-3-(p-tolylselanyl)propan-2-amine (C1) and 1-(2-methoxyphenylselanyl)-3-phenylpropan-2-amine (C2) and analogs of DPDS 1,2-bis(2-methoxyphenyl)diselenide (C3) and 1,2-bis. p-tolyldiselenide (C4). Synchronized worms at the L4 larval stage were exposed for one hour in M9 buffer to these compounds. Oxidative stress conditions were induced by juglone (200. μM) and heat shock (35. °C). Moreover, we evaluated C. elegans behavior, GST-4::GFP (glutathione S-transferase) expression and the activity of acetylcholinesterase (AChE). All tested compounds efficiently restored viability in juglone stressed worms. However, DPDS, C2, C3 and C4 significantly decreased the defecation cycle time. Juglone-induced GST-4::GFP expression was not attenuated in worms pretreated with the novel compounds, except with C2. Finally, AChE activity was reduced by DPDS, C2, C3 and C4. To our knowledge, this is study firstly showed the effects of C1, C2, C3 and C4 selenium-derived compounds in C. elegans. Low toxic effects were noted, except for reduction in the defecation cycle, which is likely associated with AChE inhibition. The juglone-induced stress (reduced viability) was fully reversed by compounds to control animal levels. C2 was also efficient in reducing the juglone-induced GST-4::GFP expression, suggesting the latter may mediate the stress induced by this compound. Future studies could be profitably directed at addressing additional molecular mechanisms that mediate the protective effects of these novel organic selenium compounds.
KW - AChE
KW - Caenorhabditis elegans
KW - Diphenyl diselenide
KW - GST-4::GFP
KW - Juglone
KW - Novel organic selenium compounds
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U2 - 10.1016/j.toxrep.2015.06.010
DO - 10.1016/j.toxrep.2015.06.010
M3 - Article
AN - SCOPUS:84937239495
SN - 2214-7500
VL - 2
SP - 961
EP - 967
JO - Toxicology Reports
JF - Toxicology Reports
ER -