Joint toxicity of fluoroquinolone and tetracycline antibiotics to zebrafish (Danio rerio) based on biochemical biomarkers and histopathological observation

• Published in: Journal of toxicological sciences 2017/06/01, Vol.42(3), pp.267-280
• Main Authors: Ding, Lihe, Zang, Luxiu, Zhang, Yuna, Zhang, Yuhuan, Wang, Xuedong, Ai, Weiming, Ding, Nani, Wang, Huili
• Format: Article
• Language: English
• Subjects: Acetylcholinesterase - metabolism; AChE activities; Animals; Anti-Bacterial Agents - toxicity; Antibiotics; Aquatic environment; Aryl Hydrocarbon Hydroxylases - genetics; Aryl Hydrocarbon Hydroxylases - metabolism; Biochemistry; Biomarkers; Control; Creatine; Creatine kinase; Creatine Kinase - metabolism; Cristae; Damage; Dose-Response Relationship, Drug; Down-Regulation - drug effects; Endoplasmic reticulum; Endoplasmic Reticulum, Rough - drug effects; Exposure; Expression of CYP3A65, AHRRa and CKma; Fluoroquinolones; Fluoroquinolones - toxicity; Gene Expression - drug effects; Hatching; Health risks; Information dissemination; Intracellular; Intracellular malondialdehyde; Liver - metabolism; Malondialdehyde; Malondialdehyde - metabolism; Mitochondria; Mitochondria - drug effects; Mitochondrial Swelling - drug effects; Oxidoreductases, N-Demethylating - genetics; Oxidoreductases, N-Demethylating - metabolism; Repressor Proteins - genetics; Reproduction - drug effects; Skeletal muscle; Skeleton; Sperm; Sperm motility; Sperm Motility - drug effects; Swelling; Tetracyclines; Tetracyclines - toxicity; Toxicity; Transcription; Transcription, Genetic - drug effects; Zebrafish; Zebrafish Proteins - genetics; Zebrafish Proteins - metabolism; β-diketone antibiotics
• ISSN: 0388-1350; 1880-3989
• DOI: 10.2131/jts.42.267

Herein, we report on the joint toxicity of four fluoroquinolones and two tetracyclines (β-diketone antibiotics-DKAs) to zebrafish based on a series of toxicological endpoints and histopathological observations. A positive dose-dependence was observed in DKA-exposure groups with a 72-hpf EC50 of 130.3 mg/L for hatching rate, 120-hpf LC50 of 149.8 mg/L, and 120-hpf EC50 of 135.1 mg/L for malformation rate. When zebrafish at 60 dpf were exposed to a series of DKA concentrations (45, 60 and 90 mg/L) for 7, 14 and 21 days, creatine kinase and AChE activities were significantly induced, and intracellular malondialdehyde increased in all treatments except for the 45 mg/L treatment. The transcription levels of AHRRa from livers were significantly (p < 0.05) up-regulated in all treatments after two months of DKA exposure. CKma expression from skeletal muscle was significantly down-regulated in the 90 mg/L treatment. A remarkable down-regulation of CYP3A65 was observed in the 60 mg/L treatment. DKA exposure resulted in severe tissue damage including mitochondria swelling, reduction of mitochondrial cristae, deepening of mitochondrial cristae bands, and decreasing and even disappearance of the rough endoplasmic reticulum. Total sperm motility was decreased by ca. 30% due to DKA exposure. These results provide important information for toxicity and health risks due to mixed DKA exposure in aquatic environments.