Dergiler / Turkish Journal of Veterinary and Animal Sciences / 2014 / Cilt: 38 - Sayı: 3

Course of hatch and developmental changes in thyroid hormone concentration in blood of chicken embryo following in ovo riboflavin supplementation

Sayfa
230–237
Yayın Tarihi
2014-05-18
DOI
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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

The data presented here suggest that riboflavin supplementation at the early stages of embryogenesis markedly affects embryonic development and influences thyroid hormone metabolism during the second half of embryogenesis.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:The influence of riboflavin on the function of the hypothalamo-pituitary-thyroid axis during chicken embryogenesis is poorly understood.
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Temel Bulgular & Veri:Eggs on the sixth day of incubation were injected with 0 (control), 60, or 600 µg of riboflavin/egg.
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Sonuç & Katkı:The data presented here suggest that riboflavin supplementation at the early stages of embryogenesis markedly affects embryonic development and influences thyroid hormone metabolism during the second half of embryogenesis.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Key words: Riboflavin · thyroid hormones · chick embryo

Özet

The influence of riboflavin on the function of the hypothalamo-pituitary-thyroid axis during chicken embryogenesis is poorly understood. Therefore, examination of the effects of in ovo riboflavin supplementation on the possible linkage between the thyroid gland function and chick embryonic development seems to be interesting. Eggs on the sixth day of incubation were injected with 0 (control), 60, or 600 µg of riboflavin/egg. Blood samples were collected on the 12th, 15th, 18th, and 20th days of embryogenesis. Thyroxine (T4) and triiodothyronine (T3) concentrations in plasma samples were determined by radioimmunoassay method. The time of external pipping and hatching of each chick as well as the body weights of sampled and newly hatched chicks were recorded. Generally, riboflavin supplied in ovo did not affect chicken embryo mortality and hatchability; however, a dose of 600 µg of riboflavin/egg had a tendency to reduce embryo body weight. Chicks exposed to 60 µg of riboflavin/egg hatched 3.7 h earlier in comparison with controls and were characterized by a higher synchronization degree of hatching. Both applied doses of riboflavin significantly elevated T4 concentrations in blood plasma of the chicken embryos; however, on day 20 of embryogenesis, both applied doses of riboflavin decreased T3 levels in blood circulation. The data presented here suggest that riboflavin supplementation at the early stages of embryogenesis markedly affects embryonic development and influences thyroid hormone metabolism during the second half of embryogenesis.

Abstract

The influence of riboflavin on the function of the hypothalamo-pituitary-thyroid axis during chicken embryogenesis is poorly understood. Therefore, examination of the effects of in ovo riboflavin supplementation on the possible linkage between the thyroid gland function and chick embryonic development seems to be interesting. Eggs on the sixth day of incubation were injected with 0 (control), 60, or 600 µg of riboflavin/egg. Blood samples were collected on the 12th, 15th, 18th, and 20th days of embryogenesis. Thyroxine (T4) and triiodothyronine (T3) concentrations in plasma samples were determined by radioimmunoassay method. The time of external pipping and hatching of each chick as well as the body weights of sampled and newly hatched chicks were recorded. Generally, riboflavin supplied in ovo did not affect chicken embryo mortality and hatchability; however, a dose of 600 µg of riboflavin/egg had a tendency to reduce embryo body weight. Chicks exposed to 60 µg of riboflavin/egg hatched 3.7 h earlier in comparison with controls and were characterized by a higher synchronization degree of hatching. Both applied doses of riboflavin significantly elevated T4 concentrations in blood plasma of the chicken embryos; however, on day 20 of embryogenesis, both applied doses of riboflavin decreased T3 levels in blood circulation. The data presented here suggest that riboflavin supplementation at the early stages of embryogenesis markedly affects embryonic development and influences thyroid hormone metabolism during the second half of embryogenesis.

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Bu Makaleye Atıf Yap

TRZECIAK, K. B., LIS, M. W., SECHMAN, A., PLYTYCZ, B., RUDOLF, A., WOJNAR, T., NIEDZIOLKA, J. W. (2014). Course of hatch and developmental changes in thyroid hormone concentration in blood of chicken embryo following in ovo riboflavin supplementation. Turkish Journal of Veterinary and Animal Sciences, Cilt: 38 - Sayı: 3, 230–237. https://ajindex.com/articles/121576

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Kaynakça (11)

  1. Massey V. The chemical and biological versatility of riboflavin. Biochem Soc Trans 2000; 28: 283–296.
  2. Plytycz B, Morgan AJ. Riboflavin storage in earthworm chloragocytes/eleocytes in an eco-immunology perspective. Inv Surv J 2011; 8: 199–209. Kidd MT. Nutritional modulation of immune function in broilers. Poultry Sci 2004; 83: 650–657. Powers HJ. Riboflavin (vitamin B-2) and health. Am J Clin Nutr 2003; 77: 1352–1360. White HB 3rd. Sudden death of chicken embryos with hereditary riboflavin deficiency. J Nutr 1996; 126: 1303S. Olkowski AA, Classen HL. The study of riboflavin requirement in broiler chickens. Int J Vitam Nutr Res 1998; 68: 316–327.
  3. Cai Z, Finnie JW, Blumbergs PC. Avian riboflavin deficiency: an acquired tomaculous neuropathy. Vet Pathol 2006; 43: 780– 7 Naber EC. Modifying vitamin composition of eggs: a review. J Appl Poult Res 1993; 2: 385–393.
  4. MacLachlan I, Nimpf J, White HB 3rd, Schneider WJ. Riboflavinuria in the rd chicken. 5’-splice site mutation in the gene for riboflavin-binding protein. J Biol Chem 1993; 268: 23222–23226.
  5. Lee CM, White HB 3rd. Riboflavin-binding protein induces early death of chicken embryos. J Nutr 1996; 126: 523–528.
  6. Lee S, McCormick DB. Thyroid hormone regulation of flavocoenzyme biosynthesis. Arch Biochem Biophys 1985; 237: 197–201.
  7. Apeland T, Kristensen O, Strandjord RE, Mansoor MA. Thyroid function during B-vitamin supplementation of patients on antiepileptic drugs. Clin Biochem 2006; 39: 282–286.
  8. Bruggeman V, Swennen Q, De Ketelaere B, Onmgabesan O, Tona K, Decuypere E. Embryonic exposure to 8-tetrachlorodibenzo-p-dioxin in chickens: effects of dose and embryonic stage on hatchability and growth. Comp Biochem Physiol C 2003; 136: 17–28.
  9. Lis MW, Sechman A, Niedziółka JW, Rząsa J. Effect of paracetamol injection in ovo on course of hatching and thyroid hormone levels in chicken embryo. B Vet I Pulawy 2006; 50: 537–542.
  10. Lis MW, Głodek K, Sechman A, Wątor D, Pawlak K, Niedziółka JW. Effect of in ovo injection of Aroclor 1254 on embryonic development, time of hatching, and blood thyroid hormone levels in one-day-old chicken. B Vet I Pulawy 2011; 55: 293– 2 Rashidi H, Sottile V. The chick embryo: hatching a model for contemporary biomedical research. BioEssays 2009; 31: 459– 4 Scanes CG, Hart LE, Decuypere E, Kuhn ER. Endocrinology of the avian embryo: an overview. J Exp Zool Suppl 1987; 1: 253–264.
  11. Darras VM, Van der Geyten S, Kühn ER. Thyroid hormone metabolism in poultry. Biotechnol Agron Soc Environ 2000; 4:13–2