Iodine and selenium supplementation increased survival and changed thyroid hormone status in Senegalese sole (Solea senegalensis) larvae reared in a recirculation system
- 379 Downloads
- 11 Citations
Abstract
To test how iodine and both iodine and selenium supplementation affected the thyroid status as well as growth and survival in Senegalese sole, larvae were reared in a recirculation system from 15 to 34 DAH. Sets of three tanks were assigned to each of the following three diets: control (C), iodine (I) and iodine and selenium (I + Se). Samples were collected at 15, 27 and 34 DAH to determine dry weight, iodine and selenium levels, GPx and ORD activities, thyroid hormone levels and thyroid follicles histology. At 34 DAH, fish from the control (C) treatment suffered from hyperplasia of the thyroid follicles (goitre), whereas iodine-treated larvae did not (I and I + Se). Lower survival rates in the C groups were probably a consequence of the hyperplasia. Moreover, there was an improvement in thyroid hormone status in I- and I + Se-treated larvae, showing that further supplementation of live feed with iodine can be crucial for fish at early life stages, as it seems to sustain normal larval development, when reared in a recirculation system. Selenium did not affect the results. Together with previous results, this indicates selenium supplement is more important at younger life stages.
Keywords
Thyroid hormones Iodine Selenium Outer-ring deiodinase Glutathione peroxidase Flatfish Recirculation systemNotes
Acknowledgments
Special thanks to senior scientist Dr. Kristin Hamre for her inputs and comments which made possible the accomplishment of this project. This work was supported by the DIGFISH project, POCI/CVT/58790/2004 (FCT, Portugal). A. R. A. Ribeiro and L. Ribeiro benefit from grants SFRH/BD/24803/2005 and SFRH/BPD/7148/2001 (FCT, Portugal), respectively. We are indebted to the highly skilled technicians at CCMAR and NIFES.
References
- Beckett GJ, Arthur JR (2005) Selenium and endocrine systems. J Endocrinol 184:455–465PubMedCrossRefGoogle Scholar
- Beckett GJ, Nicol F, Rae PW, Beech S, Guo Y, Arthur JR (1993) Effects of combined iodine and selenium deficiency on thyroid hormone metabolism in rats. Am J Clinical Nutr 57:240S–243SGoogle Scholar
- Bichsel Y, von Gunten U (1999) Determination of iodide and iodate by ion chromatography with postcolumn reaction and UV/visible detection. Ana Chem 71:34–38CrossRefGoogle Scholar
- Burel C, Boujard T, Escaffre AM, Kaushik SJ, Boeuf G, Mol KA, Van der Geyten S, Kuhn ER (2000) Dietary low-glucosinolate rapeseed meal affects thyroid status and nutrient utilization in rainbow trout (Oncorhynchus mykiss). Br J Nutr 83:653–664PubMedCrossRefGoogle Scholar
- Eales JG, Brown SB (1993) Measurement and regulation of thyroidal status in teleost fish. Rev Fish Biol Fish 3:299–347CrossRefGoogle Scholar
- Einarsdóttir I, Silva N, Power D, Smáradóttir H, Björnsson B (2006) Thyroid and pituitary gland development from hatching through metamorphosis of a teleost flatfish, the Atlantic halibut. Anat Embryol 211:47–60PubMedCrossRefGoogle Scholar
- Encinar JR, Sliwka-Kaszynska M, Polatajko A, Vacchina V, Szpunar J (2003) Methodological advances for selenium speciation analysis in yeast. Anal Chim Acta 500:171–183CrossRefGoogle Scholar
- Flohé L, Günzler A, Lester P (1984) Assays of glutathione peroxidase. Methods in enzymology. Academic Press, London, pp 114–120Google Scholar
- Hamre K, Mollan TA, Sæle Ø, Erstad B (2008a) Rotifers enriched with iodine and selenium increase survival in Atlantic cod (Gadus morhua) larvae. Aquaculture 284:190–195CrossRefGoogle Scholar
- Hamre K, Srivastava A, Ronnestad I, Mangor-Jensen A, Stoss J (2008b) Several micronutrients in the rotifer Brachionus sp may not fulfil the nutritional requirements of marine fish larvae. Aquacult Nutr 14:51–60CrossRefGoogle Scholar
- Inui Y, Yamano K, Miwa S (1995) The role of thyroid hormone in tissue development in metamorphosing flounder. Aquaculture 135:87–98CrossRefGoogle Scholar
- Julshamn K, Dahl L, Eckhoff K (2001) Determination of iodine in seafood by inductively coupled plasma/mass spectrometry. J AOAC Int 84:1976–1982PubMedGoogle Scholar
- Julshamn K, Lundebye AK, Heggstad K, Berntssen MHG, Boe B (2004) Norwegian monitoring programme on the inorganic and organic contaminants in fish caught in the Barents Sea, Norwegian Sea and North Sea, 1994 “2001. Food Additives Contaminants: Part A 21:365–376CrossRefGoogle Scholar
- Kawakami Y, Shin D-H, Kitano T, Adachi S, Yamauchi K, Ohta H (2006) Transactivation activity of thyroid hormone receptors in fish (Conger myriaster) in response to thyroid hormones. Comp Biochem Physiol Part B: Biochem Mol Biol 144:503–509CrossRefGoogle Scholar
- Klaren PHM, Haasdijk R, Metz JR, Nitsch LMC, Darras VM, Van der Geyten S, Flik G (2005) Characterization of an iodothyronine 5′-deiodinase in gilthead seabream (Sparus auratus) that is inhibited by dithiothreitol. Endocrinology 146:5621–5630PubMedCrossRefGoogle Scholar
- Klaren PHM, Wunderink YS, Yufera M, Mancera JM, Flik G (2008) The thyroid gland and thyroid hormones in Senegalese sole (Solea senegalensis) during early development and metamorphosis. Gen Comp Endocr 155:686–694PubMedCrossRefGoogle Scholar
- Kohrle J, Jakob F, Contempre B, Dumont JE (2005) Selenium, the thyroid, and the endocrine system. Endocr Rev 26:944–984PubMedCrossRefGoogle Scholar
- Leatherland JF (1994) Reflections on the thyroidology of fishes: from molecules to humankind. Guelph Ichthyol Rev 2:1–67Google Scholar
- Manchado M, Infante C, Asensio E, Planas JV, Canavate JP (2008) Thyroid hormones down-regulate thyrotropin [beta] subunit and thyroglobulin during metamorphosis in the flatfish Senegalese sole (Solea senegalensis Kaup). Gen Comp Endocr 155:447–455PubMedCrossRefGoogle Scholar
- Miwa S, Tagawa M, Inui Y, Hirano T (1988) Thyroxine surge in metamorphosing flounder larvae. Gen and Comp Endocr 70:158–163CrossRefGoogle Scholar
- Moccia RD, Leatherland JF, Sonstegard RA (1981) Quantitative interlake comparison of thyroid pathology in great lakes Coho (Oncorhynchus kisutch) and Chinook (Oncorhynchus tschawytscha) Salmon. Cancer Res 41:2200–2210PubMedGoogle Scholar
- Power DM, Llewellyn L, Faustino M, Nowell MA, Bjornsson BT, Einarsdottir IE, Canario AVM, Sweeney GE (2001) Thyroid hormones in growth and development of fish. Comp Biochem Physiol Part C: Toxicol Pharmacol 130:447–459CrossRefGoogle Scholar
- Ribeiro L, Sarasquete C, Dinis MT (1999a) Histological and histochemical development of the digestive system of Solea senegalensis (Kaup, 1858) larvae. Aquaculture 171:293–308CrossRefGoogle Scholar
- Ribeiro L, Zambonino-Infante JL, Cahu C, Dinis MT (1999b) Development of digestive enzymes in larvae of Solea senegalensis, Kaup 1858. Aquaculture 179:465–473CrossRefGoogle Scholar
- Ribeiro A, Ribeiro L, Sæle Ø, Hamre K, Dinis M, Moren M (2009) Iodine-enriched rotifers and Artemia prevent goitre in Senegalese sole (Solea senegalensis) larvae reared in a recirculation system. Aquacult Nutr 17:248–257. doi: 10.1111/j.1365-2095.2009.00740.x CrossRefGoogle Scholar
- Ribeiro ARA, Ribeiro L, Dinis MT, Moren M (2010) Protocol to enrich rotifers (Brachionus plicatilis) with iodine and selenium. Aquac Res 42. doi: 10.1111/j.1365-2109.2010.02752.x
- Sæle Ø, Solbakken JS, Watanabe K, Hamre K, Pittman K (2003) The effect of diet on ossification and eye migration in Atlantic halibut larvae (Hippoglossus hippoglossus L.). Aquaculture 220:683–696CrossRefGoogle Scholar
- Sæle Ø, Silva N, Pittman K (2006) Post-embryonic remodelling of neurocranial elements: a comparative study of normal versus abnormal eye migration in a flatfish, the Atlantic halibut. J Anat 209:31–41PubMedCrossRefGoogle Scholar
- Schreiber AM, Specker JL (1998) Metamorphosis in the summer flounder (Paralichthys dentatus): stage-specific developmental response to altered thyroid status. Gen Comp Endocr 111:156–166PubMedCrossRefGoogle Scholar
- Sherrill J, Whitaker BR, Wong GTF (2004) Effects of ozonation on the speciation of dissolved iodine in artificial seawater. J Zoo Wildlife Med 35:347–355CrossRefGoogle Scholar
- Solbakken JS, Norberg B, Watanabe K, Pittman K (1999) Thyroxine as a mediator of metamorphosis of Atlantic halibut, hippoglossus hippoglossus. Envir Biol Fishes 56:53–65CrossRefGoogle Scholar
- Sonstegard R, Leatherland JF (1976) The epizootiology and pathogenesis of thyroid hyperplasia in Coho Salmon (Oncorhynchus kisutch) in Lake Ontario. Cancer Res 36:4467–4475PubMedGoogle Scholar
- Tanaka M, Kawai S, Seikai T, Burke JS (1996) Development of the digestive organ system in Japanese flounder in relation to metamorphosis and settlement. Mar Freshw Behav Phy 28:19–31CrossRefGoogle Scholar
- Van der Geyten S, Toguyeni A, Baroiller J-F, Fauconneau B, Fostier A, Sanders JP, Visser TJ, Kühn ER, Darras VM (2001) Hypothyroidism induces type I iodothyronine deiodinase expression in Tilapia liver. Gen Comp Endocr 124:333–342PubMedCrossRefGoogle Scholar
- Witt EM, Laidley CW, Liu KKM, Hirano T, Grau EG (2009) Correlation between environmental iodide concentrations and larval growth, survival, and whole body concentrations of thyroid hormones and cortisol in Pacific threadfin (Polydactylus sexfilis). Aquaculture 289:357–364CrossRefGoogle Scholar