2008
DOI: 10.1016/j.aquatox.2007.10.014
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Copper-induced oxidative stress in rainbow trout gill cells

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Cited by 157 publications
(59 citation statements)
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“…Previous studies have shown that in response to . Previous studies have shown that in response to metal exposure, there is an increase in the formation of oxygen free radicals or reactive oxygen species (ROS) in rats, rainbow trout and M. rosenbergii (Stohs and Bagchi, 1995;Bopp et al, 2008); this can result in widespread damage to cells because of lipid peroxidation and genotoxicity. Respiratory burst, the release of reactive oxygen species (ROS) by haemocytes, is a critical step in the innate immune response.…”
Section: Discussionmentioning
confidence: 99%
“…Previous studies have shown that in response to . Previous studies have shown that in response to metal exposure, there is an increase in the formation of oxygen free radicals or reactive oxygen species (ROS) in rats, rainbow trout and M. rosenbergii (Stohs and Bagchi, 1995;Bopp et al, 2008); this can result in widespread damage to cells because of lipid peroxidation and genotoxicity. Respiratory burst, the release of reactive oxygen species (ROS) by haemocytes, is a critical step in the innate immune response.…”
Section: Discussionmentioning
confidence: 99%
“…According to Lee et al [36] this cell line allows the detailed study of both the cytotoxicity and biotransformation of chemicals that cause cytotoxicity, with a greater efficiency than an in vivo study of the gills. RTgill-W1 cells were used to evaluate the toxicity of industrial waste water, polycyclic aromatic hydrocarbons and heavy metals [37][38][39][40][41][42]. The lower sensitivity of the fish cells toward microcystins (compared to the mammalian cells) in our study could be explained with the absence of detectable mRNA levels of organic anion transporter polypeptides [43].…”
Section: Discussionmentioning
confidence: 66%
“…As many pesticides, diuron and copper may generate reactive oxygen species (ROS) and induce an overwhelming of the antioxidant system (Dautremepuits et al, 2004;Luna-Acosta et al, 2012). This oxidative stress could be accountable to reduction of cellular viability by increasing DNA strand breaks leading to apoptosis (Bopp et al, 2008) or decreasing functional integrity of the lysosomal membrane (Roméo et al, 2000;Krumschnabel et al, 2005) inducing necrosis by release of acid hydrolases (Holtzman, 1989). As discussed above, increase of cellular mortality could induce the observed impairment of phagocytosis capacity.…”
Section: Discussionmentioning
confidence: 99%