2018
DOI: 10.1016/j.aquatox.2018.10.017
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Characterization of brain acetylcholinesterase of bentonic fish Hoplosternum littorale: Perspectives of application in pesticides and metal ions biomonitoring

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Cited by 20 publications
(9 citation statements)
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“…It acts as an analog of juvenile insect hormone, a growth regulator [Ishaaya and Horowitz, 1992;World Health Organization (WHO), 2006;Chłopecka et al, 2018]. Pyriproxyfen may also act as an acetylcholinesterase inhibitor in fish (Araújo et al, 2018;Maharajan et al, 2018).…”
Section: Introductionmentioning
confidence: 99%
“…It acts as an analog of juvenile insect hormone, a growth regulator [Ishaaya and Horowitz, 1992;World Health Organization (WHO), 2006;Chłopecka et al, 2018]. Pyriproxyfen may also act as an acetylcholinesterase inhibitor in fish (Araújo et al, 2018;Maharajan et al, 2018).…”
Section: Introductionmentioning
confidence: 99%
“…vannamei and C. rhizophorae using the Ellman method with modifications . The studied drug solutions were serially diluted, with concentrations ranging from 0 to 300 μM.…”
Section: Methodsmentioning
confidence: 99%
“…The AchE inhibition studies were carried out with the commercial AChE E. electricus and the extracts obtained from L. vannamei and C. rhizophorae using the Ellman method with modifications. 29 The studied drug solutions were serially diluted, with concentrations ranging from 0 to 300 μM. In a 96-well plate, 10 μL of the compounds was incubated at varying concentrations with 10 μL of the enzyme (1 μg/mL) at 298 K for 1 h. After that time, 200 μL of DTNB (0.25 mM) and 20 μL of the acetylthiocholine iodate substrate (62 mM) were added to each well of the plate to record the absorbance at 405 nm, in order to identify the product formed from the reaction between DTNB and the substrate used.…”
Section: Methodsmentioning
confidence: 99%
“…Recently, benzoylurea, a class of pesticide that in the past was not considered an acetylcholinesterase inhibitor, since its main mode of action is the inhibition of chitin biosynthesis in insects (which interrupts the incorporation of N-acetylglycosamine monomers), demonstrated anticholinesterase potential [19]. In 2011, this class of pesticides represented 3.6% of the world's pesticide market.…”
Section: Figure 2 Organophosphate Pesticides: (A) Methyl-paration (Triesters Of Phosphoric Acid) (B) Carbamate Carbofuran (Esters Derivedmentioning
confidence: 99%