Non-steroidal anti-inflammatory drugs caused an outbreak of inflammation and oxidative stress with changes in the gut microbiota in rainbow trout (Oncorhynchus mykiss)

• Published in: The Science of the total environment Vol. 849; p. 157921
• Main Authors: Hodkovicova, N., Hollerova, A., Blahova, J., Mikula, P., Crhanova, M., Karasova, D., Franc, A., Pavlokova, S., Mares, J., Postulkova, E., Tichy, F., Marsalek, P., Lanikova, J., Faldyna, M., Svobodova, Z.
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 25.11.2022
• Subjects: Diclofenac; Gene expression; Histology; Ibuprofen; Microbiome; Toxicity; MCV; PCV; RNA; Toxicity; ALT; mRNA; Diclofenac; Ct; SD; RBC; DCF2 + IBP2; IBP; NSAIDs; Ibuprofen; IBP2; WBC; FRAP; Hb; IBP200; WWTPs; DCF; qRT-PCR; GST; SOD; TBARS; Histology; Gene expression; COX; CP; GPx; LC/MS; DCF200; MCH; DCF2; MCHC; ALB; CAT; ROS; SEM; TAG; Microbiome
• ISSN: 0048-9697; 1879-1026
• DOI: 10.1016/j.scitotenv.2022.157921

One of the main contributors to pharmaceutical pollution of surface waters are non-steroidal anti-inflammatory drugs (NSAIDs) that contaminate the food chain and affect non-target water species. As there are not many studies focusing on toxic effects of NSAIDs on freshwater fish species and specially effects after dietary exposure, we selected rainbow trout (Oncorhynchus mykiss) as the ideal model to examine the impact of two NSAIDs – diclofenac (DCF) and ibuprofen (IBP). The aim of our study was to test toxicity of environmentally relevant concentrations of these drugs together with exposure doses of 100× higher, including their mixture; and to deepen knowledge about the mechanism of toxicity of these drugs. This study revealed kidneys as the most affected organ with hyalinosis, an increase in oxidative stress markers, and changes in gene expression of heat shock protein 70 to be signs of renal toxicity. Furthermore, hepatotoxicity was confirmed by histopathological analysis (i.e. dystrophy, congestion, and inflammatory cell increase), change in biochemical markers, increase in heat shock protein 70 mRNA, and by oxidative stress analysis. The gills were locally deformed and showed signs of inflammatory processes and necrotic areas. Given the increase in oxidative stress markers and heat shock protein 70 mRNA, severe impairment of oxygen transport may be one of the toxic pathways of NSAIDs. Regarding the microbiota, an overgrowth of Gram-positive species was detected; in particular, significant dysbiosis in the Fusobacteria/Firmicutes ratio was observed. In conclusion, the changes observed after dietary exposure to NSAIDs can influence the organism homeostasis, induce ROS production, potentiate inflammations, and cause gut dysbiosis. Even the environmentally relevant concentration of NSAIDs pose a risk to the aquatic ecosystem as it changed O. mykiss health parameters and we assume that the toxicity of NSAIDs manifests itself at the level of mitochondria and proteins. [Display omitted] •Dietary exposure of DCF and IBP including their mixture was tested in O. mykiss.•IBP and DCF induced changes even at environmentally relevant concentrations.•Kidneys, liver and gills changes were observed at microscopic and molecular levels.•Overgrowth of Firmicutes and Desulfobacterota was observed in NSAIDs exposed groups.•NSAIDs probably affect mitochondrial function and cause proteotoxicity.