Synthesis of Novel Selenocyanates and Evaluation of Their Effect in Cultured Mouse Neurons Submitted to Oxidative Stress

Author:

Frizon Tiago E. A.1ORCID,Cararo José H.2,Saba Sumbal3ORCID,Dal-Pont Gustavo C.2,Michels Monique4,Braga Hugo C.5,Pimentel Tairine6,Dal-Pizzol Felipe4ORCID,Valvassori Samira S.2ORCID,Rafique Jamal6ORCID

Affiliation:

1. Department of Energy and Sustainability, Federal University of Santa Catarina (UFSC), Araranguá, 88906-072 SC, Brazil

2. Translational Psychiatry Laboratory, Graduate Program in Health Sciences, University of Southern Santa Catarina (UNESC), Criciúma, 88806-000 SC, Brazil

3. Center for Natural and Human Sciences-CCNH, Federal University of ABC (UFABC), Santo André, 09210-580 SP, Brazil

4. Laboratory of Experimental Pathophysiology, Graduate Program in Health Sciences, Health Sciences Unit, University of Southern Santa Catarina (UNESC), Criciúma. 88806-000 SC, Brazil

5. Federal University of São Paulo (UNIFESP), São José dos Campos, 12231-280 SP, Brazil

6. Institute of Chemistry, Federal University of Mato Grosso do Sul (UFMS), Campo Grande, 79074-460 MS, Brazil

Abstract

Herein, we report the synthesis of novel selenocyanates and assessment of their effect on the oxidative challenge elicited by hydrogen peroxide (H2O2) in cultured mouse neurons. First, α-methylene-β-hydroxy esters were prepared as precursors of allylic bromides. A reaction involving the generated bromides and sodium selenocyanate was conducted to produce the desired selenocyanates (3a-f). We next prepared cultures of neurons from 7-day-old mice (n=36). H2O2 (10-5 M) was added into the culture flasks as an oxidative stress inducer, alone or combined with one of each designed compounds. (PhSe)2 was used as a positive control. It was carried out assessment of lipid (thiobarbituric acid reactive species, 4-hydroxy-2-nonenal, 8-isoprostane), DNA (8-hydroxy-2-deoxyguanosine), and protein (carbonyl) modification parameters. Finally, catalase and superoxide dismutase activities were also evaluated. Among the compounds, 3b, 3d, and 3f exhibited the most pronounced pattern of antioxidant activity, similar to (PhSe)2. These novel aromatic selenocyanates could be promising to be tried in most sophisticated in vitro studies or even at the preclinical level.

Funder

Federal University of Santa Catarina

Publisher

Hindawi Limited

Subject

Cell Biology,Ageing,General Medicine,Biochemistry

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