The effect of anesthetic (2-phenoxyethanol) application on some biochemical and hematological parameters in Russian sturgeon (Acipenser gueldenstaedtii) and Siberian sturgeon (Acipenser baerii) during transport

The effect of anesthetic (2-phenoxyethanol) application on some biochemical and hematological parameters in Russian sturgeon (Acipenser gueldenstaedtii) and Siberian sturgeon (Acipenser baerii) during transport

Experiments were carried out to determine the effect of 2-phenoxyethanol to reduce stress response during the transportationof Russian and Siberian sturgeons. In transportation experiment 1 (TE1), Siberian sturgeons (687.2 ± 17.41 g) were stocked in tanksand transported for 90 min (stocking density = 65 ± 0.71 kg/m3). Before transport, 0.5 mg/L 2-phenoxyethanol was applied to the firstgroup (TE1-A, n = 285) but not to the second group (TE1-B, n = 287). In transportation experiment 2 (TE2), Russian sturgeons (1873 ±159 g) were divided into two groups and stocked in tanks as they have a density of 60 ± 0.23 kg/m3 water. Before transport, 0.6 mg/L of2-phenoxyethanol was applied to the first group (TE2-A, n = 99), the second group (TE2-B, n = 101) was left without application. Duringthe 10 h of transport period (at the 2, 4, 6, and 8 h), 0.6 mg/L 2-phenoxyethanol was applied to the fish in the first group (TE2-A) every2 h. The results revealed that plasma glucose and cortisol reached their highest level in the anesthetic-free groups (TE1-B and TE2-B)during transportation in both experiments. There was no difference in the protein levels between anesthetic and anesthetic-free groups.In the TE1-B and TE2-B, red blood cells and hematocrit decreased, neutrophils and white blood cells increased. However, no changeswere observed in eosinophils and mean corpuscular volume between groups in both experiments. Lymphocyte increased in TE1-B incomparison to TE1-A and TE1-BT (before transport anesthetic-free fish in TE1). In addition, there was no change in levels of monocyte,hemoglobin, mean hemoglobin concentration (MCH) and mean corpuscular hemoglobin concentration (MCHC) between TE1-BT, TE1-A,and TE1-B. Monocyte, hemoglobin, MCH, and MCHC increased in TE2-B compared with TE2-BT (before transport anesthetic-free fish inTE2) and TE2-A but the lymphocyte count did not change. The results indicated that the use of anesthetic agent 2-phenoxyethanol duringtransfer reduced mortality rate (0% and 12.89% in TE1-A and TE1-B, respectively, and 2.02% and 15.84% in TE2-A and TE2-B, respectively)and physiological stress in sturgeons

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  • 1. FAO (Food and Agricultural Organization). FAO-UN Fisheries and Aquaculture Information and Statistics Branch. Online Statistical Query Results 2019.
  • 2. Mylonas CC, Cardinaletti G, Sigelaki I, Polzonetti-Magni A. Comparative efficacy of clove oil and 2 phenoxyethanol as anesthetics in the aquaculture of European sea bass (Dicentrarchus labrax) and gilthead sea bream (Sparus aurata) at different temperatures. Aquaculture 2005; 246: 467-481.
  • 3. Weber RA, Peleteiro JB, Martín LG, Aldegunde M. The efficacy of 2 phenoxyethanol, metomidate, clove oil and MS-222 as anaesthetic agents in the Senegalese sole (Solea senegalensis Kaup 1858). Aquaculture 2009; 288: 147-150.
  • 4. Roubach R, Gomes LC, Leão Fonseca FA, Val AL. Eugenol as an efficacious anaesthetic for tambaqui, Colossoma macropomum (Cuvier). Aquac. Res. 2005; 36: 1056-1061.
  • 5. Duman S, Şahan A. Some hematological and non-specific immune responses of rosehip (Rosa canina)-Fed Russian Sturgeon (Acipenser gueldenstaedtii Brandt & Ratzeburg, 1833) to Mycobacterium salmoniphilum. Braz Arch Biol Technol 2018; 61: 1-17.
  • 6. Hoseini SM, Ghelichpour M. Efficacy of clove solution on blood sampling and hematological study in Beluga, Huso huso (L.). Fish Physiol Biochem 2012; 38: 493-498.
  • 7. Cataldi E, Di Marco P, Mandich A, Cataudella S. Serum parameters of Adriatic sturgeon Acipenser naccarii (Pisces: Acipenseriformes): effects of temperature and stress. Comp Biochem Phys A 1998; 121: 351-354.
  • 8. Staurnes M, Sigholt T, Pedersen HP, Rustad T. Physiological effects of simulated high-density transport of Atlantic cod (Gadus morhua). Aquaculture 1994; 119: 381-391.
  • 9. Barnett CW, Pankhurst NW. The effects of common laboratory and husbandry practices on the stress response of greenback flounder Rhombosolea tapirina (Günther, 1862). Aquaculture 1998; 162: 313-329.
  • 10. Ross LG, Ross B. Anaesthetic and sedative techniques for aquatic animals. 3rd Ed. England, UK: Oxford Blackwell Publishing; 2008.
  • 11. Robertson L, Thomas P, Arnold CR. Plasma cortisol and secondary stress responses of cultured red drum (Sciaenops ocellatus) to several transportation procedures. Aquaculture 1998; 68: 115-130.
  • 12. Barton BA, Iwama GK. Physiological changes in fish from stress in aquaculture with emphasis on the response and effects of corticosteroids. Annu Rev Fish Dis 1991; 1: 3-26.
  • 13. Barton BA. Stress in fishes: a diversity of responses with particular reference to changes in circulating corticosteroids. Integr Comp Biol 2002; 42: 517-525.
  • 14. Bukovskaya OS, Bayunova LV, Blokhin SV, Boev AA. The effects of acute stress on hormonal serum levels in Russian and stellate sturgeons during induced maturation. J Appl Ichthyol 1999; 15: 308-309.
  • 15. Affonso EG, Polez VLP, Correa CF, Mazon AF, Araujo MRR, Moraes G, Rantin FT. Blood parameters and metabolites in the teleost fish Colossoma macropomum exposed to sulfide or hypoxia. Comp Biochem Physiol C Toxicol Pharmacol 2002; 133: 375-382.
  • 16. Wendelaar Bonga SE. The stress response in fish. Physiol Rev 1997; 77: 591-625.
  • 17. Barton BA. Salmonid fishes differ in their cortisol and glucose responses to handling and transport stress. N Am J Aquacult 2000; 62: 12-18.
  • 18. Ryan JA, Hightower LE. Evaluation of heavy‐metal ion toxicity in fish cells using a combined stress protein and cytotoxicity assay. Environ Toxicol Chem 1994; 13: 1231-1240.
  • 19. Romero LM. Physiological stress in ecology: lessons from biomedical research. Trends Ecol Evol 2004; 19: 249-255.
  • 20. Webb MA, Allert JA, Kappenman KM, Marcos J, Feist GW, Schreck CB, Shackleton CH. Identification of plasma glucocorticoids in pallid sturgeon in response to stress. Gen Comp Endocr 2007; 154: 98-104.
  • 21. Tort L. Stress and immune modulation in fish. Dev Comp Immunol 2011; 35: 1366-1375.
  • 22. Iversen M, Finstad B, Nilssen KJ. Recovery from loading and transport stress in Atlantic salmon (Salmo salar L.) smolts. Aquaculture 1998; 168: 387-394.
  • 23. Iwama GK, Ackerman PA. Anaesthetics. Biochemistry and molecular biology of fishes 1994; 3: 1-15.
  • 24. Velíšek J, Svobodova Z. Anaesthesia of common carp (Cyprinus carpio L.) with 2 phenoxyethanol: acute toxicity and effects on biochemical blood profile. Acta Vet Brno 2004; 73: 247-252.
  • 25. Blaxhall PC, Daisley KW. Routine haematological methods for use with fish blood. J Fish Biol 1973; 5: 771-781.
  • 26. Trenzado CE, Carrick TR, Pottinger TG. Divergence of endocrine and metabolic responses to stress in two rainbow trout lines selected for differing cortisol responsiveness to stress. Gen Comp Endocr 2003; 133: 332-340.
  • 27. Kocabatmaz M, Ekingen G. Standardization of haematological methods and taking blood from various fish species. J of Nature Sci 1984; 2: 149-159.
  • 28. Stolen SJ, Fletcher TC, Rowley AF, Zelikoff JT, Kaattari SL, Smith, SA. Techniques in fish immunology. Fish immunology technical communications. 1st Ed. Virginia-Maryland, USA: SOS Publications; 1994.
  • 29. Blaxhall PC. The haematological assessment of the health of freshwater fish: a review of selected literature. J Fish Biol 1972; 4: 593-604.
  • 30. Fujimaki Y, Isoda M. Fine‐structural study of leucocytes in the goldfish, Carassius auratus. J Fish Biol 1990; 36: 821-831.
  • 31. Tanyer G. Hematoloji ve laboratuvar ders kitabı. Ankara, Turkey: Ayyıldız Ltd.; 1985.
  • 32. Baßmann B, Brenner M, Palm HW. Stress and welfare of African catfish (Clarias gariepinus Burchell, 1822) in a coupled aquaponic system. Water 2017; 9: 504.
  • 33. Akins RE, Levin PM, Tuan RS. Cetyltrimethylammonium bromide discontinuous gel electrophoresis: Mr-based separation of proteins with retention of enzymatic activity. Anal Biochem 1992; 202: 172-178.
  • 34. Bartoňková J, Hyršl P, Vojtek L. Glucose determination in fish plasma by two different moderate methods. Acta Vet Brno 2016; 85: 349-353.
  • 35. Düzgüneş D, Kesici T, Gürbüz F. İstatistik metodları I. Ankara, Turkey: A.Ü. Ziraat Fakültesi Yayınları; 1983 (in Turkish).
  • 36. Kayali B, Yigit M, Bulut M. Evaluation of the Recovery Time of Sea Bass (Dicentrarchus Labrax Linnaeus, 1758) Juveniles from transport and handling stress: using ammonia nitrogen excretion rates as a stress indicator. J Mar Sci Technol 2011; 19: 681-685.
  • 37. Gülen Z. Reference blood parameters values for siberian sturgeon (Acipenser baeri, Brandt 1869). MSc, Ankara University, Ankara, Turkey, 2010.
  • 38. Tavares-Dias M, Affonso EG, Oliveira SR, Marcon JL, Egami MI. Comparative study on hematological parameters of farmed matrinxã, Brycon amazonicus Spix and Agassiz, 1829 (Characidae: Bryconinae) with others Bryconinae species. Acta Amazon 2008; 38: 799-805.
  • 39. Mommsen TP, Vijayan MM, Moon TW. Cortisol in teleosts: dynamics, mechanisms of action, and metabolic regulation. Rev Fish Biol Fisher 1999; 9: 211-268.
  • 40. Barcellos LJG, Kreutz LC, de Souza C, Rodrigues LB, Fioreze I, Quevedo RM, Cericato L, Soso AB, Fagundes M, Conrad J et al. Hematological changes in jundiá (Rhamdia quelen Quoy and Gaimard Pimelodidae) after acute and chronic stress caused by usual aquacultural management, with emphasis on immunosuppressive effects. Aquaculture 2004; 237: 229-236.
  • 41. Pedron JS, Miron DS, Rodrigues RV, Okamoto MH, Tesser MB, Sampaio LA. Stress response in transport of juvenile cobia Rachycentron canadum using the anesthetic benzocaine. Lat Am J Aquat Res 2016; 44: 638-643.
  • 42. Hutchinson TH, Manning MJ. Seasonal trends in serum lysozyme activity and total protein concentration in dab (Limanda limanda L.) sampled from Lyme Bay, UK. Fish Shellfish Immunol 1996; 6: 473-482.
  • 43. Inoue LAKA, Afonso LOB, Iwama GK, Moraes G. Effects of clove oil on the stress response of matrinxã (Brycon cephalus) subjected to transport. Acta Amazon 2005; 35: 289-295.
  • 44. Shaluei F, Hedayati A, Jahanbakhshi A, Baghfalaki M. Physiological responses of great sturgeon (Huso huso) to different concentrations of 2-phenoxyethanol as an anesthetic. Fish Physiol Biochem 2012; 38: 1627-1634.
  • 45. Okafor AI, Achilefu LN. Haematological responses to stress of transportation and acclimation on the African catfish, Heterobranchus bidorsalis Geoffrey, Saint Hilare. Int Res Med Sci 2015; 3: 6-15.
  • 46. Akinrotimi OA, Ansa EJ, Owhonda KN, Onunkwo DN, Edun OM, Anyanwu PE, Opara JY, Cliffe PT. Effects of transportation stress on haematological parameters of blackchin tilapia Sarotherodon melanotheron. J Anim Vet Adv 2007; 6: 841-845.
  • 47. Adeyemo OK, Naigaga I, Alli RA. Effect of handling and transportation on haematology of African catfish (Clarias gariepinus). Journal of Fisheries Sciences 2009; 3: 333.
  • 48. Dobšíková R, Svobodova Z, Blahova J, Modra H, Velíšek J. The effect of transport on biochemical and haematological indices of common carp (Cyprinus carpio L.). Czech J Anim Sci 2009; 54: 510-518.
  • 49. Acerete L, Balasch JC, Espinosa E, Josa A, Tort L. Physiological responses in Eurasian perch (Perca fluviatilis, L.) subjected to stress by transport and handling. Aquaculture 2004; 237: 167- 178.
  • 50. Hur JW, Park IS, Chang YJ. Physiological responses of the olive flounder, Paralichthys olivaceus, to a series stress during the transportation process. Ichthyol Res 2007; 54: 32-37.
  • 51. Brinn RP, Marcon JL, McComb DM, Gomes LC, Abreu JS, Baldisseroto B. Stress responses of the endemic freshwater cururu stingray (Potamotrygon cf. histrix) during transportation in the Amazon region of the Rio Negro. Comp Biochem Phys A 2012; 162: 139-145.
  • 52. Houston AH, Roberts WC, Kennington JA. Hematological response in fish: pronephric and splenic involvements in the goldfish, Carassius auratus L. Fish Physiol Biochem 1996; 15(6): 481-489.
  • 53. Pilinkovskij A, Vosylienė MZ, Kazlauskienė N, Jakubauskaitė J. Hematological effects of transportation stress on Atlantic sturgeon Acipenser oxyrinchus Mitchill L. 1815. J Appl Ichthyol 2017 33: 1021-1023.
  • 54. Rowley AF, Hunt TC, Page M, Mainwaning G. Vertebrate blood cells. In: Rowley AF, Ratcliff NA, editors. Fish Blood Cells. London: Cambridge; Cambridge University Press; 1988. pp. 19-127.
  • 55. Siwicki AK, Morand M, Klein P, Studnicka M, Terech- Majewska E. Modulation of nonspecific defence mechanisms and protection against diseases in fish. Acta Vet Brno 1998; 67: 323-328.
  • 56. Parodi TV, Cunha MA, Becker AG, Zeppenfeld CC, Martins DI, Koakoski G, Barcellos LG, Heinzmann BM, Baldisserotto B. Anesthetic activity of the essential oil of Aloysia triphylla and effectiveness in reducing stress during transport of albino and gray strains of silver catfish, Rhamdia quelen. Fish Physiol Biochem 2014; 40: 323-334.
  • 57. Dobšíková R, Svobodová Z, Blahová J, Modrá H, Velíšek J. Stress response to long distance transportation of common carp (Cyprinus carpio L.). Acta Vet Brno 2006; 75: 437-448.
  • 58. Can E, Sümer E. Anesthetic and sedative efficacy of peppermint (Mentha piperita) and lavender (Lavandula angustifolia) essential oils in blue dolphin cichlid (Cyrtocara moorii). Turk J Vet Anim Sci 2019; 43: 334-341.
  • 59. Husen MA, Sharma S. Efficacy of anesthetics for reducing stress in fish during aquaculture practices-a review. KUSET 2014; 10: 104-123.