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As a cycloaliphatic brominated flame retardant, hexabromocyclododecane (HBCD) has been widely used in building thermal insulation and fireproof materials. However, there is little information on the bioconcentration as well as effects with respect to HBCD exposure in the aquatic environment. To investigate the bioconcentration of HBCD in tissues (muscle and liver) and its biochemical and behavioural effects, juvenile crucian carp (Carassius auratus) were exposed to different concentrations of technical HBCD (nominal concentrations, 2, 20, 200 μg/L) for 7 days, using a flow-through exposure system. HBCD was found to concentrate in the liver and muscle with a terminal concentration of 0.60 ± 0.22 μg/g lw (lipid weight) and 0.18 ± 0.02 μg/g lw, respectively, at an environmentally-relevant concentration (2 μg/L). The total thyroxine and total triiodothyronine in the fish plasma were lowered as a result of exposure to the HBCD. Acetylcholinesterase activity in the brain was increased, while swimming activity was inhibited and shoaling inclination was enhanced after exposure to 200 μg/L HBCD. Feeding rate was suppressed in the 20 and 200 μg/L treatment groups. In summary, HBCD concentrations 10-100× higher than the current environmentally-relevant exposures induced adverse effects in the fish species tested in this study. These results suggest that increasing environmental concentrations and/or species with higher sensitivity than carp might be adversely affected by HBCD. [ABSTRACT FROM AUTHOR]

The presence of pharmaceuticals in the aquatic environment has received great attention due to their potential impacts on public health. The single, as well as the combined toxicities of erythromycin (ERY) and ketoconazole (KCZ) on the bioaccumulation, biochemical and behavioral responses, were examined in crucian carp. This study focused on the uptake of contaminants, acetylcholinesterase (AChE) activity in the brain, swimming and shoaling behavior of fish. After 14 days of binary exposure, the addition of KCZ at nominal concentrations of 0.2, 2 and 20 μg/L significantly increased the accumulation of ERY in the brain of the fish and the bioconcentration factor of 2.08 was 2.6-fold higher than that calculated from the ERY-alone exposure. The brain AChE activity was significantly inhibited by ERY and KCZ with a significant correlation with respect to the accumulative concentration of the contaminants. The inhibition rates of swimming activity to KCZ were increased with a corresponding increase in the exposure concentration of KCZ in the single exposure. However, this manner was altered by the combined exposure. In addition, shoaling was significantly enhanced by KCZ-alone exposure, which was significantly correlated with the swimming activity. This study indicates that the mixture of the contaminants may cause endocrine disrupting effects and behavior modification especially in fish with known ecological and evolutionary consequences. [ABSTRACT FROM AUTHOR]

The individual and combined biochemical responses of erythromycin and ketoconazole have been examined in an organism representative of the aquatic environment, crucian carp ( Carassius auratus). The possible interactions between erythromycin and ketoconazole were investigated on the bioaccumulation and the expression of biotransformation enzymes 7-ethoxyresorufin-O-deethylase (EROD) and glutathione S-transferase (GST), and an antioxidant defense enzyme superoxide dismutase (SOD) in fish tissues. After 14 days of combined exposure (erythromycin + ketoconazole), the addition of ketoconazole at nominal concentrations of 0.2, 2, and 20 μg/L significantly increased the accumulation of erythromycin in fish bile; however, elevated erythromycin accumulation levels were not observed in the other test tissues. The inductions of EROD and SOD activity to erythromycin were inhibited by the combined exposure of ketoconazole in most cases; however, the GST activity returned to normal with exposure time and concentration of combined administration. From the tested pharmaceutical mixtures, it indicated that certain specific combinations may pose some perturbations in biochemical responses in fish and also provide a better understanding of the effects of toxic mixtures. [ABSTRACT FROM AUTHOR]

The tissue distribution, bioconcentration, metabolism and biological effects of the antifungal medication ketoconazole were investigated in fish, crucian carp ( Carassius auratus ) were exposed to a series of nominal concentrations (0.2, 2 and 20 μg/L) for 14 days. The ultra-high performance liquid chromatography tandem triple quadrupole mass spectroscopy (UPLC/MS/MS) analysis was used to determine the bioconcentration of ketoconazole and its metabolites in fish. The highest tissue concentration of ketoconazole was observed in the liver with the bioconcentration factor of 257.2, which is lower than the estimated BCF value. The ability of crucian carp to metabolize ketoconazole was confirmed and the results pointed out the existence of seven metabolites likely formed via oxidation of imidazole ring and the metabolic alteration of the piperazine rings. In addition, acetylcholinesterase, 7-ethoxyresorufin O-deethylase, superoxide dismutase and glutathione S -transferase changed significantly after 3, 7 and 14 days of exposure ( P < 0.05), which indicated that the accumulation and metabolism of ketoconazole in fish tissues may account for the biological effects. [ABSTRACT FROM AUTHOR]

Pharmaceuticals have been recognized as a new class of environmental pollutants in recent years. But data about their potential for transfer and biomagnification in aquatic food chains are still lacking. In this study, bioaccumulation of the macrolide antibiotic roxithromycin (ROX) was determined in an experimental aquatic food chain involving the green algae Scenedesmus obliquus, the water flea Daphnia magna and the crucian carp Carassius auratus. After 48 h of exposure, S. obliquus accumulated ROX from media, with bioconcentration factors (BCFs) of 74.6, 46.3, and 24.5 l kg at nominal exposure concentrations of 4, 20, and 100 μg l, respectively. After 48 h of feeding ROX-contaminated algae, D. magna was able to accumulate ROX in all three concentration treatments, but biomagnification did not occur at this trophic level, as biomagnification factors (BMFs) varied from 0.21 to 0.29 in different concentration treatments were well below one. In tissues (muscle, gill, liver, and bile) of C. auratus fed with contaminated daphnia for 8 days, no biomagnification was observed. However, this species did accumulate a certain degree of ROX through food chain transfer, and the tissue burden was greatest in the liver > muscle > gill and lowest in the bile. This work suggests that the trophic transfer should be a matter of concern for ecological risk assessments of pharmaceutical substances in aquatic food webs. [ABSTRACT FROM AUTHOR]

In this study, the tissue distribution, bioconcentration, metabolism and biological effects of the macrolide antibiotic erythromycin (ERY) were investigated in fish using crucian carp ( Carassius auratus ) as a model. Crucian carp were exposed to various concentrations of ERY (4, 20, and 100 μg/L) for 28 days. The UPLC/MS/MS analysis of both water and tissue provided the bioconcentration of ERY and its metabolites in the fish body. The results from tissue samples showed that a maximum tissue concentration occurred in the muscle and that the bioconcentration factor (BCF) of 72.2 was lower than the theoretical BCF of 90.4 calculated from the octanol-water coefficient of ERY. A significant portion of the absorbed ERY was metabolized via demethylation and dehydration and observed in the form of descladinose in fish. In addition, the relevant biomarkers, including acetylcholinesterase in the brain, as well as 7-ethoxyresorufin O-deethylase and superoxide dismutase in the liver, changed significantly during 28 days of exposure ( P < 0.05). These results clearly indicated that ERY accumulated in fish and that similar metabolites as those observed in mammals were produced, resulting in the biochemical disturbance of biological systems. [ABSTRACT FROM AUTHOR]

Highlights: [•] ROX in water could accumulate in crucian carp, particularly in liver and bile. [•] Seventeen metabolites were detected in bile. [•] A plausible scheme for biotransformation pathways of ROX in fish was depicted. [•] ROX could induce change of biomarkers, which related to ROX or its metabolites. [ABSTRACT FROM AUTHOR]

The uptake and depuration kinetics of diclofenac and carbamazepine alone at an environmentally relevant nominal concentration of 2 μg/L and in combination at a concentration ratio of 1:1 with total concentration of 4 μg/L were evaluated in Carassius carassius after 7 d uptake and depuration. Also, the biochemical effects of both drugs alone at nominal concentrations of 2 and 10 μg/L as well as in combination with total concentrations of 4 and 20 μg/L were investigated in Carassius carassius after 7 d exposure followed by 10 d recovery. In the single treatments, steady-state BCFs measured after the 7 d exposure were 73.05, 49.71, 38.01 and 24.93 L/kg for diclofenac and 9.25, 8.99, 5.29 and 4.11 L/kg for carbamazepine in the liver, brain, gill and muscle of Carassius carassius, respectively. Comparatively lower BCFs were measured in the tissues of Carassius carassius for both drugs in the combined treatments. Acetylcholinesterase activity in the brain was significantly induced by diclofenac while carbamazepine and the mixtures significantly inhibited it during all the exposure days as well as after the 10 d recovery in all treatments. This indicates that Carassius carassius could not recover from the neurotoxic effects caused by carbamazepine unlike the inductive effect caused by diclofenac which was recoverable after 10 days. A significant increase in the activities of 7-ethoxyresorufin O-deethylase and glutathione s-transferase for individual and mixed pharmaceuticals suggest that metabolism and detoxification of both drugs took place in the liver of Carassius carassius. Also, a significant increase in the activities of superoxide dismutase, catalase, glutathione reductase and malondialdehyde contents in the individual and mixture treatments mean that the antioxidant defence system of Carassius carassius was triggered to fight against oxidative stress but lipid peroxidation still occurred. However, Carassius carassius recovered from all these increases (superoxide dismutase, catalase, glutathione reductase and malondialdehyde) after the 10 d recovery, suggesting that oxidative damage is reversible. Our results indicate that both drugs at environmentally relevant concentrations might cause adverse effects in Carassius carassius and other fish species. Image 1 • Aqueous exposure of diclofenac and carbamazepine led to accumulation in the tissues of Carassius carassius. • BCFs ranged from 15.44 to 73.05 L/kg for diclofenac and 3.55–9.25 L/kg for carbamazepine.. • Carbamazepine inhibited acetylcholinesterase activity in the brain of the fish and was non-recoverable. • Both drugs were metabolised and detoxified in the liver of the fish. • Exposure to both drugs triggered the antioxidant defence system. [ABSTRACT FROM AUTHOR]

Gut microbiota plays a fundamental role in host's physiology. However, the effect of organic UV filters, an emerging contaminant on gut microbiota is poorly understood. Here, fish (Carassius auratus) were exposed to 2, 20 and 200 μg/L of benzophenone-3 (BP3) for 28 days to explore the toxicological effects and its association with the changes in the gut microbiota. The BP3 accumulation is time and dose dependent in the liver and intestine. Under BP3 subchronic exposure, fish's body and intestinal weights, reactive oxygen species (ROS), immunoglobulin M (IgM) and vitellogenin (VTG) levels, as well as 7-benzyloxy-4-trifluoromethylcoumarin-O-debenzyloxylase (BFCOD) activities, were decreased. BP3 exposure has increased the abundance of Bacteroidetes phylum and Mycobacterium genus. Bioinformatic analysis revealed that the levels of ROS, IgM, estrogen receptor and VTG, activities of lysozyme, BFCOD and 7-ethoxyresorufin-O-deethylase were significantly correlated with the relative abundance of intestinal microbial genus (p < 0.05). These results highlight for the first time the association between the effects of organic UV filters on the antioxidant, immune, endocrine, and metabolic systems of the fish and changes in the gut microbiota, which extend knowledge of the role of gut microbiota in ecotoxicology. Unlabelled Image • BP3 accumulated in fish liver, intestine and brain, causing histopathological damage. • BP3 exposure changed the number of probiotics and pathogens in the intestine. • Changes in the gut microbiota affected the immune, endocrine and metabolic systems. • BP1, BP6, BP8, DHB and 4HB were identified as metabolites of BP3 in fish liver. [ABSTRACT FROM AUTHOR]

The ubiquitous existence of hexabromocyclododecane (HBCD) in environmental matrices has made it attractive to both field investigators as well as laboratory researchers. However, literature on the biological effects caused by HBCD on aquatic vertebrates seldom exist. This has inevitably increased the difficulty of toxicological assessment in the aquatic environment. Juvenile crucian carp ( Carassius carassius ) were exposed (flow-through) to different concentrations of technical HBCD (nominal 2, 20, 200 μg L −1 ) for 7 days to determine the responses of antioxidant and biotransformation enzymes. HBCD was found to be increasingly bioconcentrated in the fish livers as time proceeds. Also, the contribution of α-HBCD exhibited an enhancement from 13% in the exposure solutions to 24% in crucian carp, still much lower than in wild fishes (ca. 80%). HBCD induced activities of antioxidant enzymes in most cases, as well as increased level of lipid peroxidation. In contrast to the weak response of 7-ethoxyresorufin-O-deethylase (EROD), 7-pentoxyresorufin-O-depentylase (PROD) activity was generally induced in a time-dependent manner with peaks at day 2. Phase II enzyme Glutathione-S-transferase (GST) showed a dose-dependent induction with maximums in the 20 μg L −1 treatment at all the four timepoints of 1, 2, 4 and 7 days. Some enzymatic responses showed good associations, indicating coordinated functions. To sum up, tHBCD exposure in the present circumstance had produced an ecological stress to crucian carp. The low levels of biotransformation and slow rates of bioisomerization suggest a possible long-term toxic effect, especially around HBCD point sources. [ABSTRACT FROM AUTHOR]

The aim of this study was to evaluate the trophic transfer of the β-blocker propranolol (PRP) in an experimental aquatic food chain involving the green algae Scenedesmus obliquus , the water flea Daphnia magna and the crucian carp Carassius auratus , as well as the metabolism and effects of PRP in the liver of crucian carp. After a 48 h PRP aqueous exposure for algae, with a subsequent 48 h dietary exposure for daphnia and an 8 d dietary exposure for crucian carp, PRP was observed in each trophic level, despite significant bioaccumulation did not occur in daphnia and crucian carp. A portion of the absorbed PRP was metabolized by the crucian carp to N -desisopropylated propranolol, propranolol glucuronic acid, monohydroxylated propranolol, hydroxypropranolol glucuronide and dihydroxypropranolol glucuronide, which were similar to those in mammals. In addition, multiple biomarkers in the liver of crucian carp (7-ethoxyresorufin O -deethylase, EROD; 7-benzyloxyresorufin O -dealkylation, BROD; superoxide dismutase, SOD and malondialdehyde, MDA) were measured. BROD and MDA were not significantly affected by PRP, while EROD and SOD did change significantly during the 8 d dietary exposure. This work indicated that the trophic transfer of PRP, resulting in biochemical perturbations of fish biological systems, should be a concern for the assessment of the environmental risks to aquatic food chains. [ABSTRACT FROM AUTHOR]

• The influences of fluoxetine on fish under environmental conditions were studied • The neurotransmission and metabolic processes in fish were simultaneously disrupted • Dissolved organic matter further intensified these disrupting effects on fish • The enhancement may be caused by binding with fluoxetine and inhibiting in metabolism Fluoxetine is a widely prescribed antidepressant that has been frequently detected in aquatic environments and is associated with a series of neurological, behavioural and neuroendocrine disruptions in nontarget organisms. However, studies on its effects in fish under realistic environmental conditions are still limited. In this study, we determined the influences of an environmentally relevant concentration of fluoxetine (100 ng/L) on crucian carp (Carassius auratus) in the presence of dissolved organic matter (DOM). Endpoints that were assessed included accumulation of fluoxetine and metabolite formation as well as related biological responses involving neurotransmission and metabolic processes. Fluoxetine was significantly bioconcentrated in the fish brain and liver and largely transformed to the active metabolite norfluoxetine. Brain neurotransmission processes related to serotonin and choline and liver metabolic status were simultaneously altered. DOM added at 1 mg/L had no effect on the accumulation of fluoxetine or its metabolites in different tissues of the fish. However, at 10 mg/L DOM facilitated fluoxetine and norfluoxetine accumulation in the liver, brain, kidney, gill and bile tissues of the fish. The neuroendocrine-disrupting effects on fish caused by fluoxetine were also enhanced by the co-addition of DOM at 10 mg/L. Binding with fluoxetine and the inhibition of metabolic functions caused by DOM may be responsible for this increase in effects. These findings imply that at high concentrations DOM can increase the toxicity of environmentally relevant concentrations of fluoxetine to fish. [ABSTRACT FROM AUTHOR]