G.S. Rieder , T. Duarte , C.P. Delgado , A. Rodighiero , P.A. Nogara , L. Orian , M. Aschner , C.L. Dalla Corte , J.B.T. Da Rocha
{"title":"Interplay between diphenyl diselenide and copper: Impact on D. melanogaster survival, behavior, and biochemical parameters","authors":"G.S. Rieder , T. Duarte , C.P. Delgado , A. Rodighiero , P.A. Nogara , L. Orian , M. Aschner , C.L. Dalla Corte , J.B.T. Da Rocha","doi":"10.1016/j.cbpc.2024.109899","DOIUrl":null,"url":null,"abstract":"<div><p>Copper (Cu<sup>2+</sup>) is a biologically essential element that participates in numerous physiological processes. However, elevated concentrations of copper have been associated with cellular oxidative stress and neurodegenerative diseases. Organo‑selenium compounds such as diphenyl diselenide (DPDS) have in vitro and in vivo antioxidant properties. Hence, we hypothesized that DPDS may modulate the toxicity of Cu<sup>2+</sup> in <em>Drosophila melanogaster.</em> The acute effects (4 days of exposure) caused by a high concentration of Cu<sup>2+</sup> (3 mM) were studied using endpoints of toxicity such as survival and behavior in <em>D. melanogaster</em>. The potential protective effect of low concentration of DPDS (20 μM) against Cu<sup>2+</sup> was also investigated. Adult flies aged 1–5 days post-eclosion (both sexes) were divided into four groups: Control, DPDS (20 μM), CuSO<sub>4</sub> (3 mM), and the combined exposure of DPDS (20 μM) and CuSO<sub>4</sub> (3 mM). Survival, biochemical, and behavioral parameters were determined. Co-exposure of DPDS and CuSO<sub>4</sub> increased acetylcholinesterase (AChE) activity and the generation of reactive oxygen species (ROS as determined by DFCH oxidation). Contrary to our expectation, the co-exposure reduced survival, body weight, locomotion, catalase activity, and cell viability in relation to control group. Taken together, DPDS potentiated the Cu<sup>2+</sup> toxicity.</p></div>","PeriodicalId":10602,"journal":{"name":"Comparative Biochemistry and Physiology C-toxicology & Pharmacology","volume":null,"pages":null},"PeriodicalIF":3.9000,"publicationDate":"2024-03-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comparative Biochemistry and Physiology C-toxicology & Pharmacology","FirstCategoryId":"93","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S153204562400067X","RegionNum":3,"RegionCategory":"环境科学与生态学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOCHEMISTRY & MOLECULAR BIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
Copper (Cu2+) is a biologically essential element that participates in numerous physiological processes. However, elevated concentrations of copper have been associated with cellular oxidative stress and neurodegenerative diseases. Organo‑selenium compounds such as diphenyl diselenide (DPDS) have in vitro and in vivo antioxidant properties. Hence, we hypothesized that DPDS may modulate the toxicity of Cu2+ in Drosophila melanogaster. The acute effects (4 days of exposure) caused by a high concentration of Cu2+ (3 mM) were studied using endpoints of toxicity such as survival and behavior in D. melanogaster. The potential protective effect of low concentration of DPDS (20 μM) against Cu2+ was also investigated. Adult flies aged 1–5 days post-eclosion (both sexes) were divided into four groups: Control, DPDS (20 μM), CuSO4 (3 mM), and the combined exposure of DPDS (20 μM) and CuSO4 (3 mM). Survival, biochemical, and behavioral parameters were determined. Co-exposure of DPDS and CuSO4 increased acetylcholinesterase (AChE) activity and the generation of reactive oxygen species (ROS as determined by DFCH oxidation). Contrary to our expectation, the co-exposure reduced survival, body weight, locomotion, catalase activity, and cell viability in relation to control group. Taken together, DPDS potentiated the Cu2+ toxicity.
期刊介绍:
Part C: Toxicology and Pharmacology. This journal is concerned with chemical and drug action at different levels of organization, biotransformation of xenobiotics, mechanisms of toxicity, including reactive oxygen species and carcinogenesis, endocrine disruptors, natural products chemistry, and signal transduction with a molecular approach to these fields.