Effects of praziquantel on common carp embryos and larvae

. 2022 Oct 14 ; 12 (1) : 17290. [epub] 20221014

Jazyk angličtina Země Velká Británie, Anglie Médium electronic

Typ dokumentu časopisecké články, práce podpořená grantem

Perzistentní odkaz   https://www.medvik.cz/link/pmid36241766
Odkazy

PubMed 36241766
PubMed Central PMC9568519
DOI 10.1038/s41598-022-21679-2
PII: 10.1038/s41598-022-21679-2
Knihovny.cz E-zdroje

This study aimed to assess the toxicity of praziquantel (anthelmintic drug) in different developmental stages of common carp (Cyprinus carpio) based on mortality, early ontogeny, growth, oxidative stress, antioxidant enzymes, histology and behaviour. Praziquantel at all tested concentrations ranging from 1 to 4 mg/L showed no significant adverse effects on mortality, the early ontogeny and behaviour locomotory (activity, moved distance and velocity) of carp after 35-day exposure. Concentrations of 3 and 4 mg/L caused significantly (P < 0.01) lower growth, total superoxide dismutase and catalase activities compared with controls. Praziquantel is safe for the early life of carp in concentrations ≤ 2 mg/L.

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Shirakashi S, Andrews M, Kishimoto Y, Ishimaru K, Okada T, Sawada Y, Ogawa K. Oral treatment of praziquantel as an effective control measure against blood fluke infection in Pacific bluefin tuna (Thunnus orientalis) Aquaculture. 2012;326:15–19. doi: 10.1016/j.aquaculture.2011.10.035. DOI

Kogiannou D, Nikoloudaki C, Rigos G. Absorption and depletion of dietary administered praziquantel in greater amberjack Seriola dumerili. Aquaculture. 2021;535:736354. doi: 10.1016/j.aquaculture.2021.736354. DOI

Morales-Serna FN, Chapa-López M, Martínez-Brown JM, Ibarra-Castro L, Medina-Guerrero RM, Fajer-Ávila EJ. Efficacy of praziquantel and a combination anthelmintic (Adecto®) in bath treatments against Tagia ecuadori and Neobenedenia melleni (Monogenea), parasites of bullseye puffer fish. Aquaculture. 2018;492:361–368. doi: 10.1016/j.aquaculture.2018.04.043. DOI

Fu G, Dong Y, Zhang X, Hu K. Metabolomic profiles and pathways of praziquantel in crucian carp. Environ. Toxicol. Pharmacol. 2020;80:103466. doi: 10.1016/j.etap.2020.103466. PubMed DOI

Maciel PO, Affonso EG. Praziquantel against monogeneans of tambaqui (Colossoma macropomum) Aquacult. Int. 2021;29:2369–2386. doi: 10.1007/s10499-021-00753-y. DOI

Rigos G, Kogiannou D, Vasilaki A, Kotsiri M. Evaluation of praziquantel efficacy against Zeuxapta seriolae infections in Greater Amberjack, Seriola dumerili. Appl. Sci. 2021;11:4656. doi: 10.3390/app11104656. DOI

Bader C, Starling DE, Jones DE, Brewer MT. Use of praziquantel to control platyhelminth parasites of fish. J. Vet. Pharmacol. Therap. 2019;42:139–153. PubMed

Baralla E, Varoni MV, Nieddu M, Demontis MP, Merella P, Burreddu C, Garippa G, Boatto G. Determination of praziquantel in Sparus aurata L. after administration of medicated animal feed. Animals. 2020;10:528. doi: 10.3390/ani10030528. PubMed DOI PMC

Farias CFS, Brandao FR, de Alexandre Sebastiao F, D Souza CM, Monteiro PC, Majolo C, Chagas EC. Albendazole and praziquantel for the control of Neoechinorhynchus buttnerae in tambaqui (Colossoma macropomum) Aquacult. Int. 2021;29:1495–1505. doi: 10.1007/s10499-021-00687-5. DOI

Kline J, Archdeacon TP, Bonar SA. Effects of praziquantel on eggs of the Asian Tapeworm Bothriocephalus acheilognathi S. N. Am. J. Aquacult. 2009;71:380–383. doi: 10.1577/A08-038.1. DOI

Sudova E, Piackova V, Velisek J, Pijacek M, Svobodova Z. Efficacy testing of orally administered praziquantel to common carp naturally infected by Caryophyllidean tapeworms (Platyhelminthes: Eucestoda) Acta Vet. Brno. 2010;79:S73–S78. doi: 10.2754/avb201079S9S073. DOI

Zuskova E, Piackova V, Machova J, Chupani L, Steinbach Ch, Stara A, Velisek J. Efficacy and toxicity of praziquantel in helminth-infected barbel (Barbus barbus L.) J. Fish Dis. 2018;41:643–649. doi: 10.1111/jfd.12764. PubMed DOI

Obiekezie A, Okafor N. Toxicity of four commonly used chemotherapeutic compounds to fry of the African catfish, Clarias gariepinus (Burchell) Aquacult. Res. 1995;26:441–445. doi: 10.1111/j.1365-2109.1995.tb00933.x. DOI

Mitchell AJ, Hobbs MS. The acute toxicity of praziquantel to grass carp and golden shiners. N. Am. J. Aquacult. 2007;69:203–206. doi: 10.1577/A06-056.1. DOI

Sudova E, Piackova V, Kroupova H, Pijacek M, Svobodova Z. The effect of praziquantel applied per os on selected haematological and biochemical indices in common carp (Cyprinus carpio L.) Fish Physiol. Biochem. 2009;35:599–605. doi: 10.1007/s10695-008-9269-3. PubMed DOI

Soltanian S, Vazirzadeh A, Akbary P. Effect of praziquantel on hemato-immunological indices in common carp (Cyprinus carpio) Iran J. Sci. Technol. Trans Sci. 2018;42:1015–1025. doi: 10.1007/s40995-017-0179-z. DOI

FAO (Food and Agriculture Organization of the United Nations) The State of World Fisheries and Aquaculture. Sustainability in Action. FAO; 2020. p. 244.

Giulio D, Hinton DE, editors. The Toxicology of Fishes. CRC Press; 2008. p. 1096.

Zrncic M, Gros M, Babic S, Kastelan-Macan M, Barcelo D, Petrovic M. Analysis of anthelmintics in surface water by ultra high performance liquid chromatography coupled to quadrupole linear ion trap tandem mass spectrometry. Chemosphere. 2014;99:224–232. doi: 10.1016/j.chemosphere.2013.10.091. PubMed DOI

Kocour M, Gela D, Rodina M, Linhart O. Testing of performance in common carp Cyprinus carpio L. under pond husbandry conditions. I: Top-crossing with Northern mirror carp. Aquacul. Res. 2005;36:1207–1215. doi: 10.1111/j.1365-2109.2005.01340.x. DOI

ARRIVE. ARRIVE guidelines. https://arriveguidelines.org/. (2022).

OECD, (Organization for Economic Cooperation and Development). Guidelines for the testing of chemicals. Section 2: Effects on Biotic Systems TG- No. 210: Fish, Early-Life Stage Toxicity Test. Paris, France, pp. 24, (2013).

Noga EJ. Fish Disease: Diagnosis and Treatment. 2. Wiley-Blackwell; 2010. p. 519.

Penaz M, Prokes M, Kouril J, Hamackova J. Early development of the carp, Cyprinus carpio. Acta Sci. Nat. Brno. 1983;17:1–39.

OECD (Organization for Economic Cooperation and Development). Guideline for Testing of Chemicals 215. Fish juvenile growth test, Paris, (2000).

Stara A, Machova J, Velisek J. Effect of chronic exposure to prometryne on oxidative stress and antioxidant response on early life stages of common carp (Cyprinus carpio L.) Neuroendocrinol. Lett. 2012;33(3):130–135. PubMed

Lushchak VI, Bagnyukova TV, Husak VV, Luzhna LI, Lushchak OV, Storey KB. Hyperoxia results in transient oxidative stress and an adaptive response by antioxidant enzymes in goldfish tissues. Int. J. Biochem. Cell. Biol. 2005;37:1670–1680. doi: 10.1016/j.biocel.2005.02.024. PubMed DOI

Marklund S, Marklund G. Involvement of superoxide anion radical in autoxidation of pyrogallol and a convenient assay for superoxide dismutase. Eur. J. Biochem. 1974;47:469–474. doi: 10.1111/j.1432-1033.1974.tb03714.x. PubMed DOI

Beers RF, Sizer IW. A spectrophotometric method for measuring the breakdown of hydrogen peroxide by catalase. J. Biol. Chem. 1952;195:133–140. doi: 10.1016/S0021-9258(19)50881-X. PubMed DOI

Habig WH, Pabst MJ, Jakoby WB. Glutathione S-transferases. First enzymatic step in mercapturic acid formation. J. Biol. Chem. 1974;249:7130–7139. doi: 10.1016/S0021-9258(19)42083-8. PubMed DOI

Carlberg I, Mannervik B. Purification and characterisation of flavoenzyme glutathione reductase from rat liver. J. Biol. Chem. 1975;250:5475–5480. doi: 10.1016/S0021-9258(19)41206-4. PubMed DOI

Tipple TE, Rogers LK. Methods for the determination of plasma or tissue glutathione levels. Meth. Mol. Biol. 2012;889:315–324. doi: 10.1007/978-1-61779-867-2_20. PubMed DOI PMC

Bradford MM. Rapid and sensitive method for the quantitation of microgram quantities of protein utilising the principle of protein dye binding. Anal. Biochem. 1976;72:248–254. doi: 10.1016/0003-2697(76)90527-3. PubMed DOI

Takashima, F. & Hibiya, T. An atlas of fish histology: normal and pathological features, second ed. Kodansha Ltd., Tokyo. pp 243 (1995).

Smith SA, editor. Fish Diseases and Medicine. 1. CRC Press; 2019. p. 398.

Nwani CD, Nnaji MC, Oluah SN, Echi PC, Nwamba HO, Ikwuagwu OE, Ajima MNO. Mutagenic and physiological responses in the juveniles of African catfish, Clarias gariepinus (Burchell 1822) following short term exposure to praziquantel. Tissue Cell. 2014;46:264–273. doi: 10.1016/j.tice.2014.05.011. PubMed DOI

Tavares-Dias M. Toxicity, physiological, histopathological and antiparasitic effects of the formalin, a chemotherapeutic of fish aquaculture. Aquacult. Res. 2021;52:1803–1823. doi: 10.1111/are.15069. DOI

Blaxter JHS. Pattern and variety in development. In: Hoar WS, Randall RJ, editors. Fish Physiology. Harcourt Brace Jovanovich; 1988. pp. 1–58.

Stancova V, Plhalova L, Bartoskova M, Zivna D, Prokes M, Marsalek P, Blahova J, Skoric M, Svobodova Z. Effects of mixture of pharmaceuticals on early life stages of tench (Tinca tinca) BioMed. Res. Int. 2014;2014:253468. doi: 10.1155/2014/253468. PubMed DOI PMC

Rico A, Phu TM, Satapornvanit K, Min J, Shahabuddin AM, Henriksson PJG, Murray FJ, Little DC, Dalsgaard A, Van den Brink PJ. Use of veterinary medicines, feed additives and probiotics in four major internationally traded aquaculture species farmed in Asia. Aquacult. 2013;412(413):231–243. doi: 10.1016/j.aquaculture.2013.07.028. DOI

Tavares-Dias M. Toxic, physiological, histomorphological, growth performance and antiparasitic effects of copper sulphate in fish aquaculture. Aquacult. 2021;535:736350. doi: 10.1016/j.aquaculture.2021.736350. DOI

McKim, J.M. Early life stage toxicity tests. in Fundamentals of Aquatic Toxicology, Effects, Environmental Fate and Risk Assessment (G.M. Rand, Ed.). (Taylor & Francis, 1995).

Woltering DM. The growth response in fish chronic and early life stage toxicity tests: a critical review. Aquat. Toxicol. 1984;5:1–21. doi: 10.1016/0166-445X(84)90028-6. DOI

Velisek J, Stara A, Kubec J, Zuskova E, Buric M, Kouba A. Effects of metazachlor and its major metabolite metazachlor OA on early life stages of marbled crayfish. Sci. Rep. 2020;10:875. doi: 10.1038/s41598-020-57740-1. PubMed DOI PMC

Velisek J, Stara A. Effect of thiacloprid on early life stages of common carp (Cyprinus carpio L.) Chemosphere. 2018;194:481–487. doi: 10.1016/j.chemosphere.2017.11.176. PubMed DOI

Stepanova S, Dolezelova P, Plhalova L, Prokes M, Marsalek P, Skorica M, Svobodova Z. The effects of metribuzin on early life stages of common carp (Cyprinus carpio) Pest. Biochem. Physiol. 2012;103:152–158. doi: 10.1016/j.pestbp.2012.04.013. DOI

Sehonova P, Plhalovaa L, Blahova J, Berankova P, Doubkova V, Prokes M, Tichy F, Vecerek V, Svobodova Z. The effect of tramadol hydrochloride on early life stages of fish. Environ. Toxicol. Pharmacol. 2016;44:151–157. doi: 10.1016/j.etap.2016.05.006. PubMed DOI

Kubec J, Kouba A, Buřič M. Communication, behaviour, and decision making in crayfish: A review. Zool. Anz. 2019;278:28–37. doi: 10.1016/j.jcz.2018.10.009. DOI

Ispir U, Kirici M, Yonar ME, Yonar MS. Response of antioxidant system to formalin in the whole body of rainbow trout, Oncorhynchus mykiss. Cell. Mol. Biol. 2017;63:13–16. doi: 10.14715/cmb/2017.63.1.3. PubMed DOI

Sakin F, Yonar SM, Yonar ME, Saglam N. Changes in selected immunological parameters and oxidative stress responses in different organs of Oncorhynchus mykiss exposed to ivermectin. Rev. Chem. 2012;63:989–995.

Thomaz JM, Martins ND, Monteiro DA, Rantin FT, Kalinin AL. Cardiorespiratory function and oxidative stress biomarkers in Nile tilapia exposed to the organophosphate insecticide trichlorfon (NEGUVON) Ecotoxicol. Environ. Safe. 2009;72:1413–1424. doi: 10.1016/j.ecoenv.2008.11.003. PubMed DOI

Yonar SM, Yonar ME, Pala A, Saglam N, Sakin F. Effect of trichlorfon on some haematological and biochemical changes in Cyprinus carpio: The ameliorative effect of lycopene. Aquacult. Rep. 2020;16:10.

Wolf JC, Wolfe MJ. A brief overview of nonneoplastic hepatic toxicity in fish. Toxicol. Pathol. 2005;33:75–85. doi: 10.1080/01926230590890187. PubMed DOI

Farrell, G.C. & Larter, C.Z. Nonalcoholic fatty liver disease: from steatosis to cirrhosis. 43, S99-112 (2006). PubMed

Purushotham A, Schug TT, Xu Q, Surapureddi S, Guo X, Li X. Hepatocyte-specific deletion of SIRT1 alters fatty acid metabolism and results in hepatic steatosis and inflammation. Cell Metab. 2009;9:327–338. doi: 10.1016/j.cmet.2009.02.006. PubMed DOI PMC

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