2001
DOI: 10.1006/pest.2001.2550
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Toxicokinetics of Malathion in Larval Stages of the Toad Bufo arenarum (Hensel): Effect of Exogenous Spermidine

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Cited by 16 publications
(7 citation statements)
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“…This is in line with the protective role classically attributed to CabEs on AChE activity, having more affinity for organophosphate binding and acting as a suicide molecule that avoids cholinesterase inactivation (Jokanović 2001;Ferrari et al 2011). Although we did not find oxidative stress induction as reported by other authors (Liendro et al 2015;Sotomayor et al 2015), we report an increase in GST activity as a detoxifying enzyme (Venturino et al 2001). In turn, GST induction might be associated with an antioxidant response that could prevent oxidative stress signs (Sotomayor et al 2015).…”
Section: Discussioncontrasting
confidence: 77%
See 1 more Smart Citation
“…This is in line with the protective role classically attributed to CabEs on AChE activity, having more affinity for organophosphate binding and acting as a suicide molecule that avoids cholinesterase inactivation (Jokanović 2001;Ferrari et al 2011). Although we did not find oxidative stress induction as reported by other authors (Liendro et al 2015;Sotomayor et al 2015), we report an increase in GST activity as a detoxifying enzyme (Venturino et al 2001). In turn, GST induction might be associated with an antioxidant response that could prevent oxidative stress signs (Sotomayor et al 2015).…”
Section: Discussioncontrasting
confidence: 77%
“…Each experimental unit consisting of 5 tadpoles per chamber was independently homogenized in 3 mL of 143 mM cold potassium phosphate buffer (pH 7.5) with 6.3 mM ethylenediaminetetraacetic acid and stored at –20 °C until processing. The following biomarkers were selected considering frequently used biochemical markers in anurans: 1) esterase activity (Venturino et al 2001) in supernatants of 10 000 g : a) acetylcholinesterase (AChE) activity, b) carboxylesterase (CabE) activity; 2) oxidative stress markers in crude homogenates: a) glutathione (GSH) levels, including reduced acid‐soluble thiols (Venturino et al 2001), b) lipid peroxide levels by thiobarbituric acid test (Venturino et al 2001); and 3) antioxidant enzymes kinetically measured in postmitochondrial supernatants at 10 000 g : a) catalase (CAT) activity (Beers and Sizer 1952; Ferrari et al 2008), b) glutathione S‐transferase (GST) activity (Habig et al 1974; Anguiano et al 2001).…”
Section: Methodsmentioning
confidence: 99%
“…However, the toxicokinetics of malathion has been reported in other species. Anuran larvae exposed to malathion in water had a comparable elimination rate, 0.0204/h, but a substantially faster absorption rate, 0.1598/min, than we found for Lumbricus [33]. Malathion is moderately hydrophobic, which can result in an increased rate of absorption from an aqueous medium in comparison to absorption from soil and the cutaneous structure of amphibian larvae is distinctly different from that of Lumbricus.…”
Section: Toxicokinetics Of Malathioncontrasting
confidence: 71%
“…However, the oxidative stress is overcome, as there is no effect on lipid peroxidation, and the ratio of reduced versus total glutathione does not change. GSH consumption is associated in this case with malathion demethylation through GST activity, which is not altered by malathion exposure in larvae (48 h) and accounts for 16% of the detoxification of this pesticide [43]. The stage-dependent increase in GSH-related antioxidant protection in the larvae is able to overcome the impact of malathion on oxidative stress in spite of the partial inactivation of GR and CAT proteins.…”
Section: Discussionmentioning
confidence: 97%