Journals / Bitlis Eren Üniversitesi Fen Bilimleri Dergisi / 2026 / Volume: 8 Issue: 1

Investigation of Oxidative Stress in Van Fish (Alburnus tarichi Guldenstadt, 1814) During Reproductive Migration

Van Balığında (Alburnus tarichi Guldenstadt, 1814) Üreme Göçü Sırasında Oksidatif Stresin Araştırılması

Necati Özok(YÜZÜNCÜ YIL ÜNİVERSİTESİ, FEN FAKÜLTESİ)
Aso Omar(VAN YÜZÜNCÜ YIL ÜNİVERSİTESİ, FEN FAKÜLTESİ)
Zehra Alkan(FACULTY OF SCIENCE)
Ayşe Nur Kıraççakalı(FACULTY OF SCIENCE)
Pages
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Publication Date
2019-03-12
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

As a result, the reactions of the organs against stress effects encountered during reproduction migration were determined.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Van Fish is an anadromous species of endemic to Turkey's largest lake.
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Key Findings & Data:The fish migrate to the freshwater pouring from the alkaline Lake Van to the lake for the reproduction every year.
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Conclusion & Impact:As a result, the reactions of the organs against stress effects encountered during reproduction migration were determined.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Van Fish · Oxidative stress · Lipid peroxidation

Abstract

Van Fish is an anadromous species of endemic to Turkey's largest lake. The fish migrate to the freshwater pouring from the alkaline Lake Van to the lake for the reproduction every year. Fish are exposed to different stress factors such as fasting, salt and pH adaptation during migration. In this study, total oxidant and antioxidant, lipid peroxidation and DNA damages in tissues such as gill, liver, plasma, brain and muscle were compared before and after reproductive migration. Total oxidant status (TOS) of the fish caught in the lake before reproduction, liver and kidney tissues, total antioxidant status (TAS), fish liver caught from freshwater, fish from the lake were observed to be high in the brain and kidney tissues (P <0.05). Malondialdehyde (MDA) levels were found to be higher in the liver and kidney of the fish sampled from the freshwater and lake, respectively. (P <0.05). DNA damage was found only in the liver of fish sampled from freshwater. As a result, the reactions of the organs against stress effects encountered during reproduction migration were determined.

Özet

Van Balığı, Türkiye’nin en büyük gölüne endemik anadrom bir türdür. Balıklar, her sene üremesini gerçekleştirmek için alkalin Van Gölünden göle dökülen tatlı sulara göç ederler. Balık bu göç sırasında açlık, tuz ve pH adaptasyonu gibi farklı stres faktörlerine maruz kalır. Bu çalışmada, Van Balığının üreme göçü öncesi ve sonrasında plazma, solungaç, karaciğer, beyin ve kas gibi dokularindaki total oksidan ve antioksidan, lipid peroksidasyon ve DNA hasarları karşılaştırıldı. Total oksidan durum (TOS) üreme öncesi gölden yakalanan balıkların karaciğer ve böbrek dokularında, total antioksidan durum (TAS) ise akarsudan yakalanan balıklarda karaciğerde, gölden yakalanan balıkların ise beyin ve böbrek dokularında yüksek olduğu gözlendi (P<0.05). Malondialdehit (MDA) seviyelerinin akarsudan örneklenen balıkların karaciğerinde gölden örneklenen balıklarda ise böbreklerinde daha fazla olduğu belirlendi (P<0.05). DNA hasarınin ise sadece tatlı sudan örneklenen balıkların karaciğerinde arttığı belirlendi. Sonuç olarak, Van Balığında üreme göçü sırasında karşılaşılan stres etkilerine karşı organların gösterdiği tepkiler belirlendi.

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Cite This Article

Oğuz, A. R., Özok, N., Omar, A., Alkan, Z., Kıraççakalı, A. N. (2019). Investigation of Oxidative Stress in Van Fish (Alburnus tarichi Guldenstadt, 1814) During Reproductive Migration. Bitlis Eren Üniversitesi Fen Bilimleri Dergisi, Volume: 8 Issue: 1. https://doi.org/10.17798/bitlisfen.512275

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References (25)

  1. Lushchak V.I. 2011. Environmentally induced oxidative stress in aquatic animals. Aquatic Toxicology, 101(1): 13-30.
  2. Birnie‐Gauvin K., Costantini D., Cooke S.J., Willmore W.G. 2017. A comparative and evolutionary approach to oxidative stress in fish: a review. Fish and Fisheries, 18(5): 928-942.
  3. Kasai H. 1997. Analysis of a form of oxidative DNA damage, 8-hydroxy-2′-deoxyguanosine, as a marker of cellular oxidative stress during carcinogenesis. Mutation Research/Reviews in Mutation Research, 387(3): 147-163.
  4. Almroth B.C., Asker N., Wassmur B., Rosengren M., Jutfelt F., Gräns A., Sundell K., Axelsson M., Sturve J. 2015. Warmer water temperature results in oxidative damage in an Antarctic fish, the bald notothen. Journal of Experimental Marine Biology and Ecology, 468: 130-137.
  5. Wilson S.M., Taylor J.J., Mackie T.A., Patterson D.A., Cooke S.J., Willmore W.G. 2014. Oxidative stress in Pacific salmon (Oncorhynchus spp.) during spawning migration. Physiological and Biochemical Zoology, 87(2): 346-352.
  6. Liu Y., Wang W.N., Wang A.L., Wang J.M., Sun R.Y. 2007. Effects of dietary vitamin E supplementation on antioxidant enzyme activities in Litopenaeus vannamei (Boone, 1931) exposed to acute salinity changes. Aquaculture, 265(1-4): 351-358.
  7. Bayir A., Sirkecioglu A.N., Bayir M., Haliloglu H.I., Kocaman E.M., Aras N.M. 2011. Metabolic responses to prolonged starvation, food restriction, and refeeding in the brown trout, Salmo trutta: oxidative stress and antioxidant defenses. Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 159(4): 191-196.
  8. Morales A.E., Pérez-Jiménez A., Hidalgo M.C., Abellán E., Cardenete G. 2004. Oxidative stress and antioxidant defenses after prolonged starvation in Dentex dentex liver. Comparative Biochemistry and Physiology Part C: Toxicology & Pharmacology, 139(1): 153-161.
  9. Rueda-Jasso R., Conceiçao L.E., Dias J., De Coen W., Gomes E., Rees J.F., Sorgeloos P. 2004. Effect of dietary non-protein energy levels on condition and oxidative status of Senegalese sole (Solea senegalensis) juveniles. Aquaculture, 231(1-4): 417-433.
  10. Danulat E, Selçuk B. 1992. Life history and enviromental conditions of the anadromous Chalcalburnus tarichi (Cyprinidae) in the highly alkaline Lake Van, Eastern Anatolia, Turkey. Arch Hidrobiol.126(1): 105–125.
  11. Kelly K.A., Havrilla C.M., Brady T.C., Abramo K.H., Levin E.D. 1998. Oxidative stress in toxicology: established mammalian and emerging piscine model systems. Environmental health perspectives, 106(7): 375-384.
  12. Slaninova A., Smutna M., Modra H., Svobodova Z. 2009. REVIEWS Oxidative stress in fish induced by pesticides. Neuroendocrinology Letters, 30(1), 2.
  13. Jain S.K., McVie R., Duett J., Herbst J.J. 1989. Erythrocyte membrane lipid peroxidation and glycosylated hemoglobin in diabetes. Diabetes, 38(12): 1539-1543.
  14. Ünal G., Çetinkaya O., Elp M. 1999. Histological investigation of gonad development of Chalcalburnus tarichi (P., 1811). Turkish Journal of Zoology, 23(EK1): 329-338. 15. Marshall W.S., Grosell M. 2006. Ion transport, osmoregulation, and acid-base balance. The physiology of fishes, 3: 177-230.
  15. Pascual P., Pedrajas J.R., Toribio F., López-Barea J., Peinado J. 2003. Effect of food deprivation on oxidative stress biomarkers in fish (Sparus aurata). Chemico-biological interactions, 145(2): 191-199.
  16. Nam Y.K., Cho Y.S., Choi B.N., Kim K.H., Kim S.K., Kim D.S. 2005. Alteration of antioxidant enzymes at the mRNA level during short‐term starvation of rockbream Oplegnathus fasciatus. Fisheries Science, 71(6): 1385-1387.
  17. Welker T.L., Congleton J.L. 2005. Oxidative stress in migrating spring Chinook salmon smolts of hatchery origin: changes in vitamin E and lipid peroxidation. Transactions of the American Fisheries Society, 134(6): 1499-1508.
  18. Hidalgo M.C., Exposito A., Palma J.M., de la Higuera M. 2002. Oxidative stress generated by dietary Zn-deficiency: studies in rainbow trout (Oncorhynchus mykiss). The international journal of biochemistry & cell biology, 34(2): 183-193.
  19. Varju M., Müller T., Bokor Z., Żarski D., Mézes M., Balogh K. 2018. The effects of excessive starvation on antioxidant defence and lipid peroxidation in intensively reared, commercial-size pikeperch (Sander lucioperca L.). The Egyptian Journal of Aquatic Research, 44(4): 349-352.
  20. Martinez-Alvarez R.M., Hidalgo M.C., Domezain A., Morales A.E., García-Gallego M., Sanz A. 2002. Physiological changes of sturgeon Acipenser naccarii caused by increasing environmental salinity. Journal of experimental biology, 205(23): 3699-3706.
  21. Martínez-Álvarez R.M., Morales A.E., Sanz A. 2005. Antioxidant defenses in fish: biotic and abiotic factors. Reviews in Fish Biology and fisheries, 15(1-2): 75-88.
  22. Barzilai A., Yamamoto, K.I. 2004. DNA damage responses to oxidative stress. DNA Repair, 3(8-9): 1109-1115.
  23. Oğuz A.R. 2015. Histological changes in the gill epithelium of endemic Lake Van Fish (Chalcalburnus tarichi) during migration from alkaline water to freshwater, North-Western Journal of Zoology 11(1):51-57.
  24. Oğuz A.R. 2013. Environmental regulation of mitochondria-rich cells in Chalcalburnus tarichi (Pallas, 1811) during reproductive migration. The Journal of membrane biology, 246(3): 183-188.
  25. Miller K.M., Schulze A.D., Ginther N., Li S., Patterson D.A., Farrell A.P., Hinch S.G. 2009. Salmon spawning migration: metabolic shifts and environmental triggers. Comparative Biochemistry and Physiology Part D: Genomics and Proteomics, 4(2): 75-89.