Andrey Massarsky

Assessment of nanosilver toxicity during zebrafish (Danio rerio) development

Nanomaterials (NMs) including silver nanoparticles (AgNPs) are incorporated into an increasing number of consumer and medical products. However, the potential toxicity of AgNPs to aquatic organisms is largely unknown. This study characterizes the effects of AgNPs on zebrafish (Danio rerio) development. The effects of silver ions (Ag(+)) and AgNPs were examined at equivalent Ag concentrations, which ranged from 0.03 to 1.55 μg mL(-1) total Ag. The Ag(+) was more toxic than AgNPs but both lead to death and delayed hatching in surviving embryos. Both silver types depleted glutathione levels but generally did not affect antioxidant enzymes activities. In addition to silver some of the embryos were also exposed to cysteine, which generally reduced the toxicity of both silver types. This study demonstrates that AgNPs and Ag(+) are capable of inducing toxicity in zebrafish embryos including the induction of oxidative stress.

Predicting the environmental impact of nanosilver

Silver nanoparticles (AgNPs) are incorporated into many consumer and medical products due to their antimicrobial properties; however, the potential environmental risks of AgNPs are yet to be fully understood. This mini-review aims to predict the environmental impact of AgNPs, thus supplementing previous reviews on this topic. To this end, the AgNP production, environmental release and fate, predicted environmental concentrations in surface water, sediment, and sludge-activated soil, as well as reported toxicity and proposed toxic mechanisms are discussed, focusing primarily on fish. Furthermore, knowledge gaps and recommendations for future research are addressed.

β-blockers as endocrine disruptors: the potential effects of human β-blockers on aquatic organisms.

β-Adrenergic blockers or β-blockers have been used therapeutically to treat human hypertension since the late 1960s. The global market value and prescription rates of β-blockers keep rising substantially each year, and over the past decade the number of prescriptions has doubled. The widespread use of β-blockers has resulted in their appearance in the aquatic environment originating primarily from sewage effluents. The objective of this review is to analyze the literature as a means to determine the endocrine-disrupting potential of β-blockers in aquatic organisms. The mammalian adrenergic system is compared with the adrenergic system of fish and the homologous octopaminergic system in aquatic invertebrates, in particular mollusks. The structure and functions of these systems are linked to the molecular similarities between adrenoceptors and the octopaminergic/tyraminergic receptors, the various catecholamine molecules (epinephrine, norepinephrine, octopamine, and tyramine), and the processes controlled. Knowledge of these similarities as well as the effects of β-blockers, mainly in humans, is then used to create a broad picture of the endocrine-disrupting potential of β-blockers, particularly during the stress response. The main conclusion is that β-blockers have endocrine-disrupting effects.

Assessment of biomarkers for contaminants of emerging concern on aquatic organisms downstream of a municipal wastewater discharge.

Contaminants of emerging concern (CECs), including pharmaceuticals, personal care products and estrogens, are detected in wastewater treatment plant (WWTP) discharges. However, analytical monitoring of wastewater and surface water does not indicate whether CECs are affecting the organisms downstream. In this study, fathead minnows (Pimephales promelas) and freshwater mussels Pyganodon grandis Say, 1829 (synonym: Anodonta grandis Say, 1829) were caged for 4 weeks in the North Saskatchewan River, upstream and downstream of the discharge from the WWTP that serves the Edmonton, AB, Canada. Passive samplers deployed indicated that concentrations of pharmaceuticals, personal care products, an estrogen (estrone) and an androgen (androstenedione) were elevated at sites downstream of the WWTP discharge. Several biomarkers of exposure were significantly altered in the tissues of caged fathead minnows and freshwater mussels relative to the upstream reference sites. Biomarkers altered in fish included induction of CYP3A metabolism, an increase in vitellogenin (Vtg) gene expression in male minnows, elevated ratios of oxidized to total glutathione (i.e. GSSG/TGSH), and an increase in the activity of antioxidant enzymes (i.e. glutathione reductase, glutathione-S-transferase). In mussels, there were no significant changes in biomarkers of oxidative stress and the levels of Vtg-like proteins were reduced, not elevated, indicating a generalized stress response. Immune function was altered in mussels, as indicated by elevated lysosomal activity per hemocyte in P. grandis caged closest to the wastewater discharge. This immune response may be due to exposure to bacterial pathogens in the wastewater. Multivariate analysis indicated a response to the CECs Carbamazepine (CBZ) and Trimethoprim (TPM). Overall, these data indicate that there is a 1 km zone of impact for aquatic organisms downstream of WWTP discharge. However, multiple stressors in municipal wastewater make measurement and interpretation of impact of CECs difficult since water temperature, conductivity and bacteria are also inducing biomarker responses in both fish and mussels.

Nanosilver cytotoxicity in rainbow trout (Oncorhynchus mykiss) erythrocytes and hepatocytes

Silver nanoparticles (AgNPs) are present in a multitude of consumer and medical products; however, the toxicity of AgNPs is not fully understood. This research aimed to elucidate the relationship between AgNP cytotoxicity and oxidative stress and damage in rainbow trout (Oncorhynchus mykiss) hepatocytes and erythrocytes in comparison to silver ions (Ag(+)). Generally the cytotoxicity of AgNPs and Ag(+) was similar, such that both silver types generated reactive oxygen species, decreased glutathione levels, and decreased activities of glutathione reductase and glutathione-S-transferase. Nonetheless, the two silver types had different cellular targets; AgNPs increased lipid peroxidation without apparent uptake into the cells whereas Ag(+) increased DNA damage. Furthermore, the toxicity of both silver types was generally decreased in cells treated with cysteine while treatment with buthionine sulfoximine increased the toxicity of both silver types.

Comparison of toxicity of uncoated and coated silver nanoparticles

This study compares toxic effects of uncoated (20, 40, 60 and 80 nm) and OECD (Organization for Economic Co-operation and Development) standard citrate- and polyvinylpyrrolidone (PVP)-coated (10, 50, and 75 nm) silver nanoparticles (Ag-NPs) in J774A. 1 macrophage and HT29 epithelial cells. The cells were exposed to different concentrations (silver content) of Ag-NPs for 24 h. Analysis showed that uncoated Ag-NPs, at a concentration of 1 μg/ml, decreased cell viability by 20–40% and that 20 and 40 nm particles were 10% more cytotoxic than the 60 and 80 nm particles. In exposures to coated Ag-NPs, cell viability dropped at 25 μg/ml or higher concentrations, and the effects were also size-dependent. PVP-coated particles induced greater cytotoxicity than citrate-coated particles. Changes in sub-cellular architecture were observed in J774A. 1 cells upon exposure to test Ag-NPs. Furthermore, uncoated Ag-NPs (1 μg/mL) decreased the expression of selected cytokines including TNF-α, IL-1β, and IL-12 (p70) in J774A. 1 and IL-8 in HT29 cells. In contrast, both citrate- and PVP-coated Ag-NPs increased the expression of these cytokines at higher concentrations (25 μg/ml), and PVP-coated particles elevated cytokine levels the most. Moreover, while uncoated Ag-NPs resulted in decreased glutathione (GSH) content and increased superoxide dismutase (SOD) activity in test cells in a size-dependent manner at 1 μg/ml, coated Ag-NPs caused non-significant changes in GSH and SOD, even at the highest test concentrations. Lastly, uncoated (20 and 40 nm) at 1 μg/ml and coated Ag-NPs (10 nm PVP) at 50 μg/ml slightly increased the production of reactive oxygen species (ROS). Our data showed that uncoated Ag-NPs are more toxic than coated Ag-NPs. While uncoated Ag-NPs appear to suppress inflammatory responses and enhance oxidative stress in the test cells, coated Ag-NPs induce toxic effects through up-regulation of cytokines. Our findings support the toxicity of Ag-NPs as being size- and coating- dependent while providing additional insight on the health impact of Ag-NPs.

Silver nanoparticles inhibit the gill Na+/K+-ATPase and erythrocyte AChE activities and induce the stress response in adult zebrafish (Danio rerio)

Silver nanoparticles (AgNPs) are the most commonly used metallic nanoparticles in industrial applications, including medical and consumer products. In the recent years, however, concerns regarding their environmental and health impacts have emerged. Aquatic organisms are of special concern since water bodies often serve as sinks for anthropogenic activities. This study assessed the effects of AgNPs on the activities of the gill Na(+)/K(+)-ATPase and erythrocyte acetylcholinestrase (AChE), as well as the plasma biochemistry in adult zebrafish (Danio rerio). In an acute exposure scenario the fish were exposed for 4d to 16.76 mg/L AgNPs, which was the 96 h LC50 value determined in preliminary experiments. In a prolonged exposure scenario the fish were exposed for 1, 2, or 3 weeks to AgNPs at concentrations of 2 and 4 mg/L, corresponding to the 1/10th and 2/10th of the 96 h LC50 value. Generally the activity of the gill Na(+)/K(+)-ATPase decreased, but this was only significant starting at 14 d of the prolonged exposure scenario, whereas the activity of the erythrocyte AChE was significantly decreased in both exposure scenarios. Finally, the plasma electrolytes levels were reduced and the plasma glucose and cortisol levels were increased in exposed fish. This study demonstrates that AgNPs could inhibit the activities of Na(+)/K(+)-ATPase and AChE, thus interfering with the proper ionoregulation and neuroregulation, respectively, and act as stressors.

The Influence of Social Status on Hepatic Glucose Metabolism in Rainbow Trout Oncorhynchus mykiss

The effects of chronic social stress on hepatic glycogen metabolism were examined in rainbow trout Oncorhynchus mykiss by comparing hepatocyte glucose production, liver glycogen phosphorylase (GP) activity, and liver β-adrenergic receptors in dominant, subordinate, control, fasted, and cortisol-treated fish. Hepatocyte glucose production in subordinate fish was approximately half that of dominant fish, reflecting hepatocyte glycogen stores in subordinate trout that were just 16% of those in dominant fish. Fasting and/or chronic elevation of cortisol likely contributed to these differences based on similarities among subordinate, fasted, and cortisol-treated fish. However, calculation of the “glycogen gap”—the difference between glycogen stores used and glucose produced—suggested an enhanced gluconeogenic potential in subordinate fish that was not present in fasted or cortisol-treated trout. Subordinate, fasted, and cortisol-treated trout also exhibited similar GP activities (both total activity and that of the active or a form), and these activities were in all cases significantly lower than those in control trout, perhaps reflecting an attempt to protect liver glycogen stores or a modified capacity to activate GP. Dominant trout exhibited the lowest GP activities (20%–24% of the values in control trout). Low GP activities, presumably in conjunction with incoming energy from feeding, allowed dominant fish to achieve the highest liver glycogen concentrations (double the value in control trout). Liver membrane β-adrenoceptor numbers (assessed as the number of 3H-CGP binding sites) were significantly lower in subordinate than in dominant trout, although this difference did not translate into attenuated adrenergic responsiveness in hepatocyte glucose production in vitro. Transcriptional regulation, likely as a result of fasting, was indicated by significantly lower β2-adrenoceptor relative mRNA levels in subordinate and fasted trout. Collectively, the data indicate that social status shapes liver metabolism and in particular glycogen metabolism, favoring accumulation of glycogen reserves from incoming energy in dominant fish and reliance on onboard fuels in subordinate fish.

Impact of a short-term diazinon exposure on the osmoregulation potentiality of Caspian roach (Rutilus rutilus) fingerlings

The stocks of Caspian roach (Rutilus rutilus), an economically important species in the Caspian Sea, are depleting. Each year millions of artificially produced fingerlings of this species are restocked in the mouth of rivers of the Southern Caspian Sea (e.g. Qare Soo River), where they are exposed to pesticides originating from regional rice and orchard fields. This early exposure to pesticides could affect the hypo-osmoregulatory ability of juvenile fish. Thus, in this study, Caspian roach fingerlings were exposed to environmentally-relevant concentrations of the organophosphate insecticide diazinon for 96 h in fresh water and then transferred to diazinon-free brackish water (BW) for another 96 h. We report that cortisol and glucose levels were significantly increased in all diazinon treatments at all sampling time points in comparison to the control group. Moreover, the thyroid hormone levels of TSH, T4, and T3 significantly decreased in diazinon-exposed fish even after the transfer to BW. The electrolytes were differentially affected during the exposure to diazinon and after the transfer to BW. The number of chloride cells in the gill tissue was significantly increased during diazinon exposure at the higher concentrations and decreased to control levels after transfer to BW. Finally, gill and kidney tissues showed many histopathological changes in diazinon-exposed fish even after 240 h in BW. These results suggest that the release of Caspian roach fingerlings into the diazinon-contaminated Caspian Sea regions may alter their physiology and jeopardize their survival, which could lead to a failure in rebuilding the Caspian roach stocks in the Caspian Sea.

Exposure to gemfibrozil and atorvastatin affects cholesterol metabolism and steroid production in zebrafish (Danio rerio).

The commonly used lipid-lowering pharmaceuticals gemfibrozil (GEM) and atorvastatin (ATV) are detected in the aquatic environment; however, their potential effects on non-target fish species are yet to be fully understood. This study examined the effects of GEM and/or ATV on female and male adult zebrafish after a 30d dietary exposure. The exposure led to changes in several biochemical parameters, including reduction in cholesterol, triglycerides, cortisol, testosterone, and estradiol. Changes in cholesterol and triglycerides were also associated with changes in transcript levels of key genes involved with cholesterol and lipid regulation, including SREBP2, HMGCR1, PPARα, and SREBP1. We also noted higher CYP3A65 and atrogin1 mRNA levels in drug-treated male fish. Sex differences were apparent in some of the examined parameters at both biochemical and molecular levels. This study supports these drugs affecting cholesterol metabolism and steroid production in adult zebrafish. We conclude that the reduction in cortisol may impair the ability of these fish to mount a suitable stress response, whereas the reduction of sex steroids may negatively affect reproduction.