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Transferability of oxytetracycline (OTC) from feed to carp muscle and evaluation of the antibiotic effects on antioxidant systems in liver and kidney

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Abstract

Oxytetracycline (OTC) is employed in fish farms to contest or prevent bacterial infections. We simulated an OTC treatment at therapeutic level (75 mg kg−1) and at higher doses (150, 300 mg kg−1) for 10 days. A withdrawal period of 10 days was considered for treated carp, carrying out the same chemical and biochemical analyses (total glutathione, superoxide dismutase, catalase, glutathione peroxidase, glutathione reductase, glutathione S-transferase and malondialdehyde). The aim was to obtain data related to the carryover in muscle and on variations in the antioxidant indicators in liver and kidney. The OTC residual levels in muscle showed a dose–response relationship. After 10 days of treatment at the recommended dose (75 mg kg−1), the mean value in muscle was 295 μg kg−1. After 10 withdrawal days, residues in all treated groups were not entirely eliminated by fish. Residues of recommended 75 mg kg−1 OTC dose were lower than the maximum permitted by EEC regulation: 100 μg kg−1. Disturbance in the antioxidant systems in liver and kidney was recorded in (150, 300 mg kg−1) carp, as well as during the withdrawal period. A lowered superoxide dismutase activity and higher levels of catalase, glutathione peroxidase, glutathione reductase and glutathione were evaluated in liver, while in kidney only higher malondialdehyde and glutathione S-transferase concentrations were recorded for 300 mg kg−1 dose. The therapeutic OTC dose exerted lower effects, and only in liver, enhancement of GPx and GR activities was recorded. After the withdrawal period, altered antioxidant responses in tissues were restored for all three OTC doses.

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References

  • Bounias M, Kładny J, Kruk I, Michalska T (1997) Hydroxyl radical generation during oxidation of catecholamines and dopa. Toxicol Environ Chem 60:163–169

    Article  CAS  Google Scholar 

  • Chi ZX, Liu R, Zhang H (2010) Potential enzyme toxicity of oxytetracycline to catalase. Sci Tot Environ 408:5399–5404

    Article  CAS  Google Scholar 

  • Commission Decision 2002/657/EC Off. J. Eur. Communities 2002, L221

  • Cristofani E, Antonini C, Tovo G, Fioroni L, Piersanti A, Galarini R (2009) A confirmatory method for the determination of tetracyclines in muscle using high-performance liquid chromatography with diode-array detection. Anal Chim Acta 637:40–46

    Article  CAS  PubMed  Google Scholar 

  • EEC Regulation n. 2377/90

  • Elia AC, Mantilacci L, Taticchi MI, Principato G (1999) Characterization of the major glutathione transferases in carp liver. J Exp Zool 284:130–136

    Article  CAS  Google Scholar 

  • Elia AC, Mantilacci L, Natali M, Principato G (2000) Association of glutathione peroxidase activity with an acidic glutathione S-transferase in carp liver. Ital J Zool 67:39–43

    Article  CAS  Google Scholar 

  • Elia AC, Galarini R, Taticchi MI, Dörr AJM, Mantilacci L (2003) Antioxidant responses and bioaccumulation in Ictalurus melas under mercury exposure. Ecotox Environ Saf 55:162–167

    Article  CAS  Google Scholar 

  • Elia AC, Galarini R, Dörr AJM, Carnevali O, Fioroni L, Taticchi MI (2005) Polychlorinated biphenyls and antioxidant enzymes in liver of Cyprinus carpio L. from Lake Trasimeno. Ital J Zool 72:1–7

    Article  CAS  Google Scholar 

  • Elia AC, Anastasi V, Dörr AJM (2006a) Hepatic antioxidant enzymes and total glutathione of Cyprinus carpio exposed to three disinfectants, chlorine dioxide, sodium hypochlorite and peracetic acid, for superficial water potabilization. Chemosphere 64:1633–1641

    Article  CAS  PubMed  Google Scholar 

  • Elia AC, Galarini R, Dörr AJM, Taticchi MI (2006b) Bioaccumulation of heavy metals, organochlorine pesticides and detoxificant biochemical indexes in tissues of Ictalurus melas of Lake Trasimeno. Bull Environ Contam Toxicol 76:132–139

    Article  CAS  PubMed  Google Scholar 

  • Elia AC, Dörr AJM, Galarini R (2007) Comparison of organochlorine pesticides, PCBs and heavy metal contamination and of detoxifying response in tissues of Ameiurus melas from Corbara, Alviano and Trasimeno Lakes, Italy. Bull Environ Contam Toxicol 78:463–468

    Article  CAS  PubMed  Google Scholar 

  • Elia AC, Fanetti A, Dörr AJM, Taticchi MI (2008) Effects of concentrated drinking water on glutathione and glutathione-dependent enzymes in Cyprinus carpio L. Chemosphere 72:791–796

    Article  CAS  PubMed  Google Scholar 

  • Elia AC, Dörr AJM, Abete MC, Prearo M (2010) Seasonal variability of detoxificant response and heavy metal accumulation in tissues of both sexes in Tinca tinca (L.) from Lake Trasimeno. Rev Fish Biol Fisher 20:425–434

    Article  Google Scholar 

  • Elia AC, Prearo M, Pacini N, Dörr AJM, Abete MC (2011) Effects of selenium diets on growth, accumulation and antioxidant response in juvenile carp. Ecotox Environ Saf 74:166–173

    Article  CAS  Google Scholar 

  • Fagutao FF, Yasuike M, Santos MD, Ruangpan L, Sangrunggruang K, Tassanakajon A, Takahashi Y, Ueno R, Kondo H, Hirono I, Aoki T (2009) Differential gene expression in black tiger shrimp, Penaeus monodon, following administration of oxytetracycline and oxolinic acid. Develop Comp Immunol 33:1088–1092

    Article  CAS  Google Scholar 

  • Khan MA, Mustafa J, Musarrat J (2003) Mechanism of DNA strand breakage induced by photosensitised tetracycline-Cu(II) complex. Mut Res/Fund Mol Mech Mutag 525:109–119

    Article  CAS  Google Scholar 

  • Kładna A, Michalska T, Berczyński P, Kruk I, Aboul-Enein HY (2012) Evaluation of the antioxidant activity of tetracycline antibiotics in vitro. Luminescence 27:249–255

    Google Scholar 

  • Kraus RL, Pasieczny R, Lariosa-Willingham K, Turnek MS, Jiang A, Trauger JW (2005) Antioxidant properties of minocycline: neuroprotection in an oxidative stress assay and direct radical-scavenging activity. J Neurochem 94:819–827

    Article  CAS  PubMed  Google Scholar 

  • Lin S, Wei X, Xu Y, Yan C, Dodel R, Zhang Y, Liu J, Klauning JE, Farlow M, Du Y (2003) Minocycline blocks 6-hydroxydopamine-induced neurotoxicity and free radical production in rat cerebellar granule neurons. Life Sci 72:1635–1641

    Article  CAS  PubMed  Google Scholar 

  • Lowry OH, Rosebrough NJ, Farr AL, Randall RJ (1951) Protein measurement with the Folin phenol reagent. J Biol Chem 193:265–275

    CAS  PubMed  Google Scholar 

  • Lunden T, Miettinen S, Lonnstrom LG, Lilius EM, Bylund G (1998) Influence of oxytetracycline and oxolinic acid on the immune response of rainbow trout (Oncorhynchus mykiss). Fish Shellfish Immunol 8:217–230

    Article  Google Scholar 

  • Malvisi J, della Rocca G, Anfossi P, Giorgetti G (1996) Tissue distribution and residue depletion of oxytetracycline in sea bream (Sparus aurata) and sea bass (Dicentrarchus labrax) after oral administration. Aquaculture 147:159–168

    Article  CAS  Google Scholar 

  • McCord JM, Fridovich I (1969) Superoxide dismutase: an enzymatic function for erythrocuprein (hemocuprein). J Biol Chem 244:6049–6055

    CAS  PubMed  Google Scholar 

  • Miller RA, Pelsor FR, Kane AS, Reimschuessel R (2012) Oxytetracycline pharmacokinetics in rainbow trout during and after an orally administered medicated feed regimen. J Aquat Animal Health 24:121–128

    Article  CAS  Google Scholar 

  • Namdari R, Abedini S, Law FCP (1996) Tissue distribution and elimination of oxytetracycline in seawater chinook and coho salmon following medicated-feed treatment. Aquaculture 144:27–38

    Article  CAS  Google Scholar 

  • Nimmo IA (1987) The glutathione S-transferases of fish. Fish Physiol Biochem 3:163–172

    Article  CAS  PubMed  Google Scholar 

  • Pacini N, Abete MC, Dörr AJM, Prearo M, Natali M, Elia AC (2012) Detoxifying response in juvenile tench fed by selenium diet. Environ Toxicol Pharmacol 33:46–52

    Article  CAS  PubMed  Google Scholar 

  • Pacini N, Prearo M, Abete MC, Brizio P, Dörr AJM, Reimschuessel R, Andersen W, Gasco L, Righetti M, Elia AC (2013) Antioxidant responses and renal crystal formation in rainbow trout treated with melamine administered individually or in combination with cyanuric acid. J Toxicol Environm Health A 76:491–508

    Article  CAS  Google Scholar 

  • Paschoal JAR, Bicudo ÁJA, Cyrino JEP, Reyes FGR, Rath S (2012) Depletion study and estimation of the withdrawal period for oxytetracycline in tilapia cultured in Brazil. J Vet Pharmacol Therap 35:90–96

    Article  CAS  Google Scholar 

  • Petrenko I, Titov VI, Vladimirov IA (1995) Generation of active forms of oxygen by antibiotics of the tetracycline series during tetracycline catalysis of oxidation of ferrous ion. Antibiot Khimioter 40:3–8

    CAS  PubMed  Google Scholar 

  • Quinlan G, Gutteridge JM (1988) Hydroxyl radical generation by the tetracycline antibiotics with free radical damage to DNA, lipids and carbohydrate in the presence of iron and cooper salts. Free Rad Biol Med 5:341–348

    Article  CAS  PubMed  Google Scholar 

  • Rawles SD, Kocabas A, Gatlin DM, Du WX, Wei CI (1997) Dietary supplementation of terramycin and Romet-30 does not enhance growth of channel catfish but does influence tissue residues. J World Aqua Soc 28:392–401

    Article  Google Scholar 

  • Rigos G, Nengas I, Tyrpenou AE, Alexis M, Troisi GA (2003) Pharmacokinetics and bioavailability of oxytetracycline in gilthead sea bream (Sparus aurata) after a single dose. Aquaculture 221:75–83

    Article  CAS  Google Scholar 

  • Saglam N, Yonar ME (2009) Effects of sulfamerazine on selected haematological and immunological parameters in rainbow trout (Onchorhynchus mykiss, Walbaum, 1792). Aquaculture Res 40:395–404

    Article  CAS  Google Scholar 

  • Segner H, Sundh H, Buchmann K, Douxfils J, Sundell KS, Mathieu C, Ruane N, Jutfelt F, Toften H, Vaughan L (2012) Health of farmed fish: its relation to fish welfare and its utility as welfare indicator. Fish Physiol Biochem 38:85–105

    Article  CAS  PubMed  Google Scholar 

  • Shaw JP, Large AT, Donkin P, Evans SV, Staff FJ, Livingstone DR, Chipman JK, Peters LD (2004) Seasonal variation in cytochrome P450 immunopositive protein levels, lipid peroxidation and genetic toxicity in digestive gland of the mussel Mytilus edulis. Aquat Toxicol 67:325–336

    Article  CAS  PubMed  Google Scholar 

  • Sies H (1999) Glutathione and its role in cellular functions. Free Radic Biol Med 27:916–921

    Article  CAS  PubMed  Google Scholar 

  • Topic Popovic N, Howell T, Babish JG, Bowser PR (2012) Cross-sectional study of hepatic CYP1A and CYP3A enzymes in hybrid striped bass, channel catfish and Nile tilapia following oxytetracycline treatment. Res Vet Sci 92:283–291

    Article  CAS  PubMed  Google Scholar 

  • Villarini M, Moretti M, Dominici L, Fatigoni C, Dörr AJM, Elia AC, Monarca S (2011) A protocol for the evaluation of genotoxicity in bile of carp (Cyprinus carpio) exposed to lake water treated with different disinfectants. Chemosphere 84:1521–1526

    Article  CAS  PubMed  Google Scholar 

  • Wang Q, Liu Q, Li J (2004) Tissue distribution and elimination of oxytetracycline in perch Lateolabrax japonicus and black seabream (Sparus macrocephalus) following oral administration. Aquaculture 237:31–40

    Article  CAS  Google Scholar 

  • Yonar ME (2012) The effect of lycopene on oxytetracycline-induced oxidative stress and immunosuppression in rainbow trout (Oncorhynchus mykiss, W.). Fish Shellfish Immunol 32:994–1001

    Article  CAS  PubMed  Google Scholar 

  • Yonar EM, Yonar MS, Silici S (2011) Protective effect of propolis against oxidative stress and immunosuppression induced by oxytetracycline in rainbow trout (Oncorhynchus mykiss, W). Fish Shellfish Immunol 31:318–325

    Article  Google Scholar 

  • Zhang Q, Li X (2007) Pharmacokinetics and residue elimination of oxytetracycline in grass carp, Ctenopharyngodon idellus. Aquaculture 272:140–145

    Article  CAS  Google Scholar 

  • Zhang X, Xie P, Li D, Tang R, Lei H, Zhao Y (2009) Time-dependent oxidative stress responses of crucian carp (Carassius auratus) to intraperitoneal injection of extracted microcystins. Bull Environ Contam Toxicol 82:574–578

    Article  CAS  PubMed  Google Scholar 

  • Zounková R, Klimešová Z, Nepejchalová L, Hilscherová K, Bláha L (2011) Complex evaluation of ecotoxicity and genotoxicity of antimicrobials oxytetracycline and flumequine used in aquaculture. Environ Toxicol Chem 30(5):1184–1189

    Article  PubMed  Google Scholar 

Download references

Acknowledgments

The work was financially supported by “Ministero della Salute” and co-financed by “Fondo Sociale Europeo (FSE) nell’ambito del Programma Operativo Regionale (POR) Umbria, FSE Obiettivo Competitività Regionale e Occupazione 2007–2013,” Italy.

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Correspondence to Antonia Concetta Elia.

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Elia, A.C., Ciccotelli, V., Pacini, N. et al. Transferability of oxytetracycline (OTC) from feed to carp muscle and evaluation of the antibiotic effects on antioxidant systems in liver and kidney. Fish Physiol Biochem 40, 1055–1068 (2014). https://doi.org/10.1007/s10695-013-9905-4

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