Determination of Niclosamide and its Metabolites in Liver and Muscles of Common Carp (Cyprinus carpio) Fingerlings
DOI:
https://doi.org/10.22456/1679-9216.80635Keywords:
niclosamide residues, distribution, common carp, liver, muscles.Abstract
Background: Niclosamide is a medication used to treat tapeworm infestation in animals and humans. It is also lampricide and molluscicide, and can be used in in agriculture as a pesticide. In the treatment of parasitic diseases in fish, niclosamide can be used as bath or mixed with the feed. Its most important use in common carp (Cyprinus carpio) is for the treatment of Bothriocephalus acheilognathi, which is a very common parasite in this fish species. The aim of this study was to determine the concentrations of niclosamide (NIC) and its metabolite 2-chloro 4-nitro aniline (CNA) and 5-chloro salycilic acid (CSA) in the liver and muscles of common carp fingerlings.
Materials, Methods & Results: The fish for the experiment were obtained from Kapetanski Rit fish pond, and were acclimated to test conditions at 20.5 ± 1°C. Common carps with an average mass of 60 ± 10 g were treated with niclosamide in concentration of 2 g/kg of feed during five consecutive days. The experiment was performed in two treatments: one control and niclosamide, in three replications. Each group contained of 30 fish, in 120 L polyethylene tanks. At the end of the treatment, the levels of niclosamide residues were determined using a high performance liquid chromatography (HPLC) analysis during over 13 days. The mean values of niclosamide and CNA concentrations in the muscles ranged from 27.7 µg/kg starting from the first day to <0.5 µg/kg on the 11th day and 14.2 µg/kg from the first day to <1 µg/kg on the 9th day. The CSA metabolite in muscles were <1 µg/kg during throughout the entire study. The niclosamide concentration in the liver were found to be 51.5 (30.2-61.8) µg/kg the first day and decreased proportionally to <0.5 µg/kg on the13th day. CNA level in the liver of treated Common Carps amounted to 170.1 (157-181) µg/kg on the first day and continuously declined until the 13th day when recorded values were <1 µg/kg. The CSA concentrations in the liver reached a maximum level of 11.5 (10.1-12.8) µg/kg on the 7th day and fell to <1 µg/kg on the 13th day.
Discussion: Niclosamide use in fish is questionable, primarily due to the possible toxic effects on some aquatic organisms. In Serbia, niclosamide preparation for use in aquaculture, has been produced by Veterinarski zavod Subotica since 1984 when it was registred for the first time. Niclosamid degradation mechanism showed that the metabolism of niclosamide resulted in two main metabolites CNA and CSA. Withdrawal of niclosamide and its residues in the liver and muscle in the present investigation lasted from 9 to 13 days. This decrease in residues concentrations is expected and depends primarily on several factors such as the length and concentration of drug with which the fish is treated, biotransformation, excretion and decomposition of used drug. Niclosamide and CNA were proportionally decreased during the withdrawal time, while the CSA value increased to the seventh day although the fish during this period no longer consumed food with niclosamide, after which the value then decreased until the end of its elimination. This is also not unexpected because it is known that liver and gallbladder is a major organ for collection, storage and elimination of chemical residues. Although the treated fish received 2 mg of the niclosamide per g of feed for five consecutive days results obtained in this study indicate that the maximal residues concentrations were much lower than doses of niclosamide that each fish absorbed into the body. Data obtained during this study provided information about the concentration and withdrawal times of niclosamide and its residues CNA and CSA in the liver and muscles of common carp treated orally.
Downloads
References
Abreu F.C., Goulart M.O.F. & Oliveira Brett A.M. 2002. Detection of the damage caused to DNA by niclosamide using an electrochemical DNA-biosensor. Biosensors and Bioelectronics. 17(11-12): 913-919.
Al-Hadiya B.M. 2005. Niclosamide: comprehensive profile. Profiles of Drug Substances, Excipients, and Related Methodology. 32: 67-96. [Fonte:<http://dx.doi.org/10.1016/S0099-5428(05): 32002-8]. [Accessed online July 2016].
Andrews P., Thyssen J. & Lorke D. 1982. The biology and toxicology of molluscicides, Bayluscide. Pharmacology & Therapeutics. 19(2): 245-295.
Ćirković M., Kartalović B., Novakov N., Pelić M., Đorđević V., Radosavljević V. & Aleksić N. 2015. Distribution of niclosamide residues in meat and internal organs of common carp. In: Procedia Food Science, Proceedings of the 58th International Meat Industry Conference Meat Safety and Quality: Where it goes? (Belgrade, Serbia). pp.54-56.
Datta G. & Bera T. 2000. The effects of clofazimine, niclosamide and amphotericin B, on electron transport of Leishmania donovani promastigotes. The Indian Journal of Medical Research. 112: 15-20.
Dawson K.V. 1982. Accumulation and loss of 2’ ,5-dichloro-4’-nitrosalicylanilide (Bayer 73) by fish: laboratory studies (Report: Investigations in Fish Control 90). La Crosse: Fish and Wildlife Service, pp.1-5.
Dawson K.V., Schreier T.M., Boogaard M.A. & Gingerich W.H. 1999. Uptake, metabolism, and elimination of niclosamide by fish. In: Xenobiotics in Fish. La Crosse: Springer, pp.167-176.
Gowrisankar D. & Rao N.M. 2014. Development and validation of stability indicating RP-HPLC and UV-spectroscopy methods for quantitative determination of niclosamide in pharmaceutical dosage forms. Journal of Global Trends in Pharmaceutical Sciences. 5(1): 1460-1465.
Li Y., Li P.K., Roberts M.J., Arend R.C., Samant R.S. & Buchsbaum D.J. 2014. Multi-targeted therapy of cancer by niclosamide: A new application for an old drug. Cancer Letters. 349(1): 8-14.
Liu C., Armstrong C., Zhu Y., Lou W. & Gao A.C. 2016. Niclosamide enhances abiraterone treatment via inhibition of androgen receptor variants in castration resistant prostate cancer. Oncotarget. 7(22): 32210-32220.
Martin R.J. 1997. Modes of action of anthelmintic drugs. Veterinary journal. 154(1): 11-34.
Oliveira-Filho E.C. & Paumgartten F.J. 2000. Toxicity of Euphorbia milli latex and niclosamide to snails and nontarget aquatic species. Ecotoxicology Environmental Safety. 46(3): 342-350.
Rajamuthiah R., Fuchs B.B., Conery A.L., Kim W., Jayamani E., Kwon B., Ausubel F.M., & Mylonakis E. 2015. Repurposing salicylanilide anthelmintic drugs to combat drug resistant Staphylococcus aureus. PLoS One. 10(4): e0124595.
Rotzinger S., Bourin M., Akimoto Y., Coutts R.T. & Baker G.B. 1999. Metabolism of some “second”- and “fourth”generation antidepressants: iprindole, viloxazine, bupropion, mianserin, maprotiline, trazodone, nefazodone, and venlafaxine. Cellular and Molecular Neurobiology. 19(4): 427-442.
Schmahl G. & Taraschewski H. 1987. Treatment of fish parasites: effects of praziquantel, niclosamide, levamisole-HCl, and metrifonate on monogenea (Gyrodactylus aculeati, Diplozoon paradoxum). Parasitology Research. 73(4): 341-351.
Schreier T.M., Dawson V.K., Choi Y., Spanjers N.J & Boogaard M.A. 2000. Determination of niclosamide residues in rain bow trout (Oncorhynchus mykiss) and channel catfish (Ictalurus punctatus) fillet tissue by high-performance liquid chromatography. Journal of Agricultural and Food Chemistry. 48(6): 2212-2215.
Swan G.E. 1999. The pharmacology of halogenated salicylanilides and their anthelmintic use in animals. Journal of the South African Veterinary Association-Tydskrif van die Suid-afrikaanse Veterinere Vereniging. 70(2): 61-70.
Treves-Brown K.M. 2000. Applied Fish Pharmacology. Dordrecht: Kluwer Academic Publishers, 308p.
Tripathi K.D. 2008. Essentials of Medical Pharmacology. 6th edn. New Delhi: Jaypee Brothers Medical Publishers Ltd., 917p.
Xu M., Lee E.M., Wen Z., Cheng Y., Huang W.K., Qian X., Tcw. J., Kouznetsova J., Ogden S.C., Hammack C., Jacob F., Nguyen H.N., Itkin M., Hanna C., Shinn P., Allen C., Michael S.G., Simeonov A., Huang W., Christian K.M., Goate A., Brennand K.J., Huang R., Xia M., Ming G.L., Zheng W., Song H. & Tang H. 2016. Identification of small-molecule inhibitors of Zika virus infection and induced neural cell death via a drug repurposing screen. Nature Medicine. 22(10): 1101-1107.
Zazaa H., Abdelrahman M., Ali N., Magdy M.A. & Abdelkawy M. 2014. Kinetic study and mechanism of niclosamide degradation. Spectrochimica Acta part A: Molecular and Biomolecular Spectroscopy. 11(132): 655-662.
Published
How to Cite
Issue
Section
License
This journal provides open access to all of its content on the principle that making research freely available to the public supports a greater global exchange of knowledge. Such access is associated with increased readership and increased citation of an author's work. For more information on this approach, see the Public Knowledge Project and Directory of Open Access Journals.
We define open access journals as journals that use a funding model that does not charge readers or their institutions for access. From the BOAI definition of "open access" we take the right of users to "read, download, copy, distribute, print, search, or link to the full texts of these articles" as mandatory for a journal to be included in the directory.
La Red y Portal Iberoamericano de Revistas Científicas de Veterinaria de Libre Acceso reúne a las principales publicaciones científicas editadas en España, Portugal, Latino América y otros países del ámbito latino