2018
DOI: 10.1016/j.chemosphere.2018.04.082
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Tissue bioconcentration and effects of fluoxetine in zebrafish (Danio rerio) and red crucian cap (Carassius auratus) after short-term and long-term exposure

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Cited by 47 publications
(21 citation statements)
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“…Basic pharmaceuticals such as the selected serotonin reuptake inhibitors fluoxetine and sertraline, secondary amines with a pK a > 9.5 like the ionizable alkylamines studied here, accumulate to greater extents in the liver than in the muscle of fish exposed to sewage treatment plant effluents, 41,42 but not in fish subjected to controlled exposure. 43 Also amitriptyline, a phospholipophilic tertiary amine-based drug (pK a 9.8, log D MW 3.9) 44 showed higher accumulation in fish liver than in muscle (gilt-head bream) in a controlled bioconcentration study, 45 but the liver/plasma concentration ratios were not as high as the D L−B observed here. Higher values of D L−B compared to D Mus−B have also been observed for chloroquine, a basic pharmaceutical, and attributed to greater lysosomal sequestration in liver cells, 38 a process that has also been demonstrated for basic psychotropic drugs in slices of various rat tissues.…”
Section: ■ Resultsmentioning
confidence: 49%
“…Basic pharmaceuticals such as the selected serotonin reuptake inhibitors fluoxetine and sertraline, secondary amines with a pK a > 9.5 like the ionizable alkylamines studied here, accumulate to greater extents in the liver than in the muscle of fish exposed to sewage treatment plant effluents, 41,42 but not in fish subjected to controlled exposure. 43 Also amitriptyline, a phospholipophilic tertiary amine-based drug (pK a 9.8, log D MW 3.9) 44 showed higher accumulation in fish liver than in muscle (gilt-head bream) in a controlled bioconcentration study, 45 but the liver/plasma concentration ratios were not as high as the D L−B observed here. Higher values of D L−B compared to D Mus−B have also been observed for chloroquine, a basic pharmaceutical, and attributed to greater lysosomal sequestration in liver cells, 38 a process that has also been demonstrated for basic psychotropic drugs in slices of various rat tissues.…”
Section: ■ Resultsmentioning
confidence: 49%
“…Human excretion of up to 10% of FLX parent compound and conjugated FLX glucuronide via the urine [1] and/or improper disposal have been reported to result in untreated urban WWTP influent concentrations of FLX as high as 3 μg/L [11]. In exposed fish, bioconcentration occurs and can reach factors >100, especially in slightly alkaline water conditions [13,15,35]. Tissue concentrations of FLX and its active metabolite NFLX are highest in brain and liver of wild-caught fish, reaching levels as high as 10 ng/g for FLX and 20 ng/g for NFLX [11,12,14].…”
Section: Introductionmentioning
confidence: 99%
“…Pseudorasbora parva juveniles exposed for 42 days to 200 µg/L fluoxetine also displayed GST inhibition in the liver and gills [44]. The reduction in the activity of biotransformation enzymes could be related to the negative regulation of genes involved in the detoxification pathways, as observed by Cunha et al (2016) [40]. The effects of fluoxetine on antioxidant responses and biotransformation processes have been widely reported, with increased or decreased activity of enzymes belonging to these groups (CAT, SOD, GSH/GSSH, LPO/MDA, GST, and EROD activity).…”
Section: Discussionmentioning
confidence: 90%
“…The effects of fluoxetine on antioxidant responses and biotransformation processes have been widely reported, with increased or decreased activity of enzymes belonging to these groups (CAT, SOD, GSH/GSSH, LPO/MDA, GST, and EROD activity). The different fluoxetine concentrations tested, exposure lengths, species, and life stages tested may be related to the variability of responses [40][41][42][43][44]46]. However, all these studies evidence and support the potential of fluoxetine to promote long-term biochemical effects.…”
Section: Discussionmentioning
confidence: 96%
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