Journals / Turkish Journal of Veterinary and Animal Sciences / 2005 / Cilt: 29 - Sayı: 3

Ultrastructural Effects of Retinyl Palmitate on Brown Adipocytes of Fetal Mice

Pages
629–634
Publication Date
2005-03-01
DOI
—
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AI Summary & Key Takeaways

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

In conclusion, this study indicated that vitamin A derivative applied in therapeutic dose during pregnancy accelerates the developmental period of BAT adipocytes in fetal mice.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Brown adipose tissue (BAT) has a thermogenic function in animals.
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Key Findings & Data:Mitochondrial uncoupling protein (UCP) is responsible for the thermogenic function in BAT cells.
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Conclusion & Impact:In conclusion, this study indicated that vitamin A derivative applied in therapeutic dose during pregnancy accelerates the developmental period of BAT adipocytes in fetal mice.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Retinoic acid · brown adipocyte · ultrastructure

Abstract

Brown adipose tissue (BAT) has a thermogenic function in animals. Mitochondrial uncoupling protein (UCP) is responsible for the thermogenic function in BAT cells. Vitamin A affects proliferation and differentiation in cells. Retinoic acid, a derivative of vitamin A, stimulates the expression of the UCP gene, which is found in BAT cells. Retinoic acid performs its function regardless of differentiation stage of BAT cells. It is known that vitamin A is teratogenic at therapeutic doses in pregnancy. In this study, effects of retinyl palmitate applied in a therapeutic dose were examined in mice fetal BAT cells. Tissue samples were subjected to a routine electron microscopic procedure for this purpose and then examined. In the control group cells, mitochondria were found to have short cristae, the glycogen granules occupying the cytoplasm were large and the same as those in developing BAT cells, and the lipid granules were few. Glycogen granules constituted smaller clusters in the cytoplasm of cells in the vitamin A group. As compared with the control group, cristae of mitochondria were elongated and matured. In this group, the amount of lipid granules was more striking than that in the control group. In conclusion, this study indicated that vitamin A derivative applied in therapeutic dose during pregnancy accelerates the developmental period of BAT adipocytes in fetal mice.

Özet

Brown adipose tissue (BAT) has a thermogenic function in animals. Mitochondrial uncoupling protein (UCP) is responsible for the thermogenic function in BAT cells. Vitamin A affects proliferation and differentiation in cells. Retinoic acid, a derivative of vitamin A, stimulates the expression of the UCP gene, which is found in BAT cells. Retinoic acid performs its function regardless of differentiation stage of BAT cells. It is known that vitamin A is teratogenic at therapeutic doses in pregnancy. In this study, effects of retinyl palmitate applied in a therapeutic dose were examined in mice fetal BAT cells. Tissue samples were subjected to a routine electron microscopic procedure for this purpose and then examined. In the control group cells, mitochondria were found to have short cristae, the glycogen granules occupying the cytoplasm were large and the same as those in developing BAT cells, and the lipid granules were few. Glycogen granules constituted smaller clusters in the cytoplasm of cells in the vitamin A group. As compared with the control group, cristae of mitochondria were elongated and matured. In this group, the amount of lipid granules was more striking than that in the control group. In conclusion, this study indicated that vitamin A derivative applied in therapeutic dose during pregnancy accelerates the developmental period of BAT adipocytes in fetal mice.

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Cite This Article

ÖZOĞUL, C., KÖKSAL, M., ERDOĞAN, D. (2005). Ultrastructural Effects of Retinyl Palmitate on Brown Adipocytes of Fetal Mice. Turkish Journal of Veterinary and Animal Sciences, Cilt: 29 - Sayı: 3, 629–634. https://ajindex.com/articles/136109

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References (10)

  1. Afzelius, A.B.: Brown adipose tissue: Its gross anatomy, histology, cytology. In: Lindberg, O. Ed. Brown Adipose Tissue, American Elsevier Publishing, New York. 1970; 1-31
  2. Alvarez, R., de Anjes, J., Yuberto, P., Vinas, O., Mampel, T., Iglesias, R., Girald, M., Villarroya, F.: A novel regulatory pathway of brown fat thermogenesis. Retinoic acid is a transcriptional activator of the mitochondrial uncoupling protein gene. J. Biol. Chem., 1995; 270: 5666-5673
  3. Hernandez, A., Garcia-Jimenez, C., Santisteban, P., Obregon, M.J.: Regulation of malic-enzyme-gene expression by cAMP and retinoic acid in differentiating brown adipocytes. Eur. J. Biochem., 1993; 215: 285-290. 8. Rabelo, R., Reyes, C., Schifman, A., Silva, J.E.: A complex retinoic acid element in the uncoupling protein gene defines a novel role for retinoids in thermogenesis. Endocrinology, 1996; 137: 88-96
  4. Serra, F., Bonet, M.L., Puigserver, P., Oliver, J., Palou, A.: Stimulation of uncoupling protein 1 expression in brown adipocytes by naturally occuring carotenoids. Int. J. Obes. Relat. Metab. Disord., 1999; 23: 650-655.
  5. Alvarez, R., Checa, M., Brun, S., Vinas, O., Mampel, T., Iglesias, R., Giralt, M., Villarroya, F.: Both retinoic-acid-receptor and retinoid-X-receptor-dependent signaling pathways mediate the induction of the brown-adipose-tissue-ucoupling-protein-1 gene by retinoids. Biochem. J., 2000; 345: 91-97.
  6. Bonet, M.L., Oliver, J., Pico, C., Felipe, F., Ribot, J., Cinti, S., Palou, A.: Opposite effects of feeding a vitamin A deficient diet and retinoic acid treatment on brown adipose tissue uncoupling protein-1 (UCP-1), UCP-2 and leptin expression. J. Endocrinol., 2000; 166: 511-517.
  7. Scarpace P.J., Mathney, M., Moore, R.L., Kumar, M.V.: Modulation of uncoupling protein 2 and uncoupling protein 3: Regulation by denervation, leptin and retinoic acid treatment. J. Endocrinol., 2000; 164: 331-337.
  8. Abbott, B.D., Hil, L.G., Birnbaum, L.S.: Processes involved in retinoic acid production of small embryonic palatal shelves and limb defects. Teratology, 1990; 41: 299-310.
  9. Kochhar, D.M., Penner, J.D., Satre, M.A.: Derivation of retinoic acid and metabolites from a teratonogenic dose of retinol (vitamin A) in mice. Toxicol. Appl. Pharmacol., 1988; 96: 429-441.
  10. Creech Kraft, J., Lofberg, B., Chahoud, I., Bochert, G., Nau, H.: Teratogenicity and placental transfer of all-trans-,13-cis-, 4-oxo- all-trans-, and 4-oxo-13-cis-retinoic acid after administration of a low oral dose during organogenesis in mice. To