Bedoukian   RussellIPM   RussellIPM   Piezoelectric Micro-Sprayer


Home
Animal Taxa
Plant Taxa
Semiochemicals
Floral Compounds
Semiochemical Detail
Semiochemicals & Taxa
Synthesis
Control
Invasive spp.
References

Abstract

Guide

Alphascents
Pherobio
InsectScience
E-Econex
Counterpart-Semiochemicals
Print
Email to a Friend
Kindly Donate for The Pherobase

« Previous AbstractHow climate change and wildlife management affect population structure in wild boars    Next AbstractThe main and accessory olfactory systems of female mice are activated differentially by dominant versus subordinate male urinary odors »

Toxicol In Vitro


Title:"Analysis of oxidative stress in SK-N-MC neurons exposed to styrene-7,8-oxide"
Author(s):Vettori MV; Caglieri A; Goldoni M; Castoldi AF; Dare E; Alinovi R; Ceccatelli S; Mutti A;
Address:"ISPESL Research Center at the University of Parma, via Gramsci 14, Parma 43100, Italy. mariavittoria.vettori@unipr.it"
Journal Title:Toxicol In Vitro
Year:2005
Volume:19
Issue:1
Page Number:11 - 20
DOI: 10.1016/j.tiv.2004.04.015
ISSN/ISBN:0887-2333 (Print) 0887-2333 (Linking)
Abstract:"Styrene-7,8-oxide (SO) is the main metabolite of styrene, a neurotoxic volatile organic compound used industrially. Here we report the novel observation that several markers of oxidative stress were affected in SK-N-MC cells exposed for 16 h to concentrations of SO that induce apoptotic cell death. The production of Thiobarbituric Acid Reactive Substances (TBARS), rose from 69.1 +/- 15.7 nmol/g protein (control) to 119.3 +/- 39.2 and 102.0 +/- 17.3 nmol/g protein after exposure to 0.3 and 1 mM SO, respectively. Carbonyl group levels were significantly enhanced by SO at both concentrations. The lower dose also decreased sulphydryl groups. SO caused a marked oxidative DNA damage, as shown by a fivefold increase in 8-hydroxy-2(')-deoxyguanosine (8-OHdG). In addition, SO exposure resulted in alterations of scavenging abilities, given the reduction of both glutathione (GSH) and glutathione-S-transferase (GST) activity. Induction of expression of the oxidative stress response gene heme-oxygenase-1 (HO-1) and an increased HO-1 activity were also observed. These data provide compelling evidence that oxidative stress significantly contributes to SO toxicity in neuronal cells"
Keywords:"8-Hydroxy-2'-Deoxyguanosine Biomarkers/metabolism Carcinogens/*toxicity Cell Line, Tumor DNA Damage Deoxyguanosine/*analogs & derivatives/metabolism Dose-Response Relationship, Drug Epoxy Compounds/*toxicity Free Radical Scavengers/metabolism Glutathione/;"
Notes:"MedlineVettori, M V Caglieri, A Goldoni, M Castoldi, A F Dare, E Alinovi, R Ceccatelli, S Mutti, A eng Research Support, Non-U.S. Gov't England 2004/12/08 Toxicol In Vitro. 2005 Feb; 19(1):11-20. doi: 10.1016/j.tiv.2004.04.015"

 
Back to top
 
Citation: El-Sayed AM 2024. The Pherobase: Database of Pheromones and Semiochemicals. <http://www.pherobase.com>.
© 2003-2024 The Pherobase - Extensive Database of Pheromones and Semiochemicals. Ashraf M. El-Sayed.
Page created on 29-06-2024