2015
DOI: 10.1016/j.ecoenv.2015.03.010
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Toxicological effects and oxidative stress responses in freshwater snail, Lanistes carinatus, following exposure to chlorpyrifos

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Cited by 52 publications
(19 citation statements)
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References 36 publications
(31 reference statements)
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“…The results observed in the present study imply that probably in the metabolism of chlorpryifos in the freshwater snails H. duryi, ROS were indeed produced and probably that caused the defense mechanism of the snails to be activated (indicated by activation of CAT, GPX and GST) probably as an adaptive mechanism to overcome the oxidative stress induced effects of chlorpyrifos. Our results are supported by Khalil [32] who also reported induction of CAT, GPX and GST in the freshwater snail Lanistes carinatus exposed to the organophosphorus insecticide chlorpyrifos.…”
Section: Discussionsupporting
confidence: 81%
“…The results observed in the present study imply that probably in the metabolism of chlorpryifos in the freshwater snails H. duryi, ROS were indeed produced and probably that caused the defense mechanism of the snails to be activated (indicated by activation of CAT, GPX and GST) probably as an adaptive mechanism to overcome the oxidative stress induced effects of chlorpyrifos. Our results are supported by Khalil [32] who also reported induction of CAT, GPX and GST in the freshwater snail Lanistes carinatus exposed to the organophosphorus insecticide chlorpyrifos.…”
Section: Discussionsupporting
confidence: 81%
“…They indirectly protect cells against the adverse effects of xenobiotics, carcinogens and toxic radicals (Griffith, 1999). Lipid peroxidation has been suggested to play a role in metal toxicity, with numerous studies undertaken using malondialdehyde (MDA) as biomarker of oxidative stress (Steven and Nerishi, 1992;Khalil, 2015 andOgunka-Nnoka et al, 2018).…”
Section: Discussionmentioning
confidence: 99%
“…After 96 h exposure, shrimps of each experimental tank were collected, and brain, hepatopancreas, gills, and muscles were dissected, cleaned and immediately washed with ice-cold saline. Samples were weighed and homogenized in ice-cold Potassium Phosphate Buffer (50mM, pH 7.5, EDTA 60mM) [25] containing protease inhibitor (Sigma P2714) by using a glass homogenizer. Then, the homogenate was centrifuged at 3600 rpm for 15 min at 4˚C [KUBOTA (3700), Japan] and the supernatant corresponding to the post-mitochondrial fraction was used to evaluate enzymatic (CAT, GR, GST) and lipid peroxidation levels (LPO).…”
Section: Tissue Preparation For Antioxidant Enzymes Assaysmentioning
confidence: 99%
“…chlorpyrifos [60][61][62]. The observed LPO resulting from exposure to chlorpyrifos may lead to cell death [25]. Hence, L vannamei can be used as a test organism for in situ assessment of lipid oxidation.…”
Section: Plos Onementioning
confidence: 99%