2019
DOI: 10.1016/j.scitotenv.2018.10.079
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Evaluation of the estrogen receptor alpha as a possible target of bifenthrin effects in the estrogenic and dopaminergic signaling pathways in zebrafish embryos

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Cited by 28 publications
(10 citation statements)
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“…50,55−57 Furthermore, reduced DHA affects ion channels and several neurotransmitter receptors, such as those involved in the dopaminergic pathway, 58,59 which have previously been reported to be dysregulated following bifenthrin treatment. 13,14,20,27 Adenine levels were significantly reduced in steelhead exposed to both 60 and 120 ng/L bifenthrin. Purine ribonucleoside degradation and adenine and adenosine salvage I and III were among the top predicted canonical pathways impaired in steelhead treated with bifenthrin.…”
Section: ■ Discussionmentioning
confidence: 96%
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“…50,55−57 Furthermore, reduced DHA affects ion channels and several neurotransmitter receptors, such as those involved in the dopaminergic pathway, 58,59 which have previously been reported to be dysregulated following bifenthrin treatment. 13,14,20,27 Adenine levels were significantly reduced in steelhead exposed to both 60 and 120 ng/L bifenthrin. Purine ribonucleoside degradation and adenine and adenosine salvage I and III were among the top predicted canonical pathways impaired in steelhead treated with bifenthrin.…”
Section: ■ Discussionmentioning
confidence: 96%
“…DHA, also acting as the primary ligand for the activation of the retinoid X receptor (RXR), was a top canonical pathway predicted to be affected in chlorpyrifos-methyl-exposed Atlantic salmon (Salmo salar). Increased RXR receptor activation may alter lipid metabolism and inflammatory responses . Decreased levels of DHA reduced the escape behavior in gilthead sea bream (Sparus aurata), where decreased levels may be related to reduced sensory perception, stimulus transmission, and neuronal-specific responses, cognitive function, and olfactory function. , Furthermore, reduced DHA affects ion channels and several neurotransmitter receptors, such as those involved in the dopaminergic pathway, , which have previously been reported to be dysregulated following bifenthrin treatment. ,,, …”
Section: Discussionmentioning
confidence: 99%
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“…The primary mode of action for bifenthrin is binding to and disrupting voltage-gated Na + channels, impairing neuronal function by altering the release of neurotransmitters [ 25 , 26 , 27 ]. Bifenthrin is a known endocrine disruptor in fish [ 28 , 29 , 30 , 31 , 32 ], dysregulating the hypothalamic-pituitary-gonadal (HPG) and hypothalamic-pituitary-thyroid (HPT) axis in salmonids by acting upon the dopaminergic pathway [ 20 , 21 , 22 , 31 ]. Bifenthrin is also capable of dysregulating Ca 2+ homeostasis by impairing signaling molecules, as recently reported in inland silversides ( Menidia beryllina ) and zebrafish ( Danio rerio ) following bifenthrin treatment (<10 ng/L) [ 33 , 34 ].…”
Section: Introductionmentioning
confidence: 99%