DOI QR코드

DOI QR Code

Effect of Lactic Acid Extracts of Sargassum horneri on Bone Formation in Female Sprage-Dawley Rats

평생이모자반 젖산 추출물이 성장기 암컷흰쥐의 골 형성에 미치는 영향

  • Jun, Joon-Young (Department of Marine Food Science and Technology, Gangneung-Wonju National University) ;
  • Lee, Su-Young (Department of Marine Food Science and Technology, Gangneung-Wonju National University) ;
  • Kim, Byeng-Mok (Korea Food Research Institute) ;
  • Jeong, In-Hak (Department of Marine Food Science and Technology, Gangneung-Wonju National University)
  • 전준영 (강릉원주대학교 해양식품공학과) ;
  • 이수영 (강릉원주대학교 해양식품공학과) ;
  • 김병목 (한국식품연구원) ;
  • 정인학 (강릉원주대학교 해양식품공학과)
  • Received : 2010.11.15
  • Accepted : 2011.02.10
  • Published : 2011.02.28

Abstract

We investigated the effect of a lactic acid extract of Sargassum horneri (ExSL) as a calcium supplement on bone formation in 48 female Sprague-Dawley rats for 4 weeks of their growth phase. The rats were divided into four groups based on diet: two calcium-sufficient and two calcium-deficient diets. The normal control group (NC) was fed AIN-93G; the NCS group was fed the same diet containing 1% extract; the calcium-deficient control (DC) diet was based on AIN-93G; and the DCS group received the same calcium-deficient diet plus 1% extract. Bone formation in the rats was evaluated using the wet weight, length, diameter, and bone mineral density (BMD) of the femur. Serum parameters were also examined. The food intake among the groups did not differ significantly (P<0.05). The NCS group gained the most body weight, while the DC group gained much less weight than the other groups. The feeding efficiencies of the groups that received the extract (NCS and DCS) were slightly higher than those of the control groups (NC and DC). The calcium intakes of all groups depended on the amount of calcium in the feed; the NCS and DCS diets contained 12.15 mg more calcium than the NC and DC diets. The calcium absorption was lower in NCS than in DC and DCS, but significantly higher than in NC (P<0.05). The BMDs in the calcium-sufficient groups were not significantly different (P<0.05), while in the calcium-deficient groups the BMD was significantly higher in DCS than in DC (P<0.05). The serum calcium and phosphorus levels in all groups were not associated with markers of bone growth related to the extract. The osteocalcin content and alkaline phosphatase (ALPase) activity were higher in the calcium-deficient groups than in the normal groups (P<0.05). Ultimately, the osteocalcin content and ALPase activity were lower in DCS compared to DC. These results suggest that the addition of ExSL promotes bone formation and calcium absorption in growing rats.

Keywords

References

  1. AOAC. 1990. Official Method of Analysis. 15thed. Association of Official Analytical Chemists, Washington, DC, U.S.A., Vol 17, 868-931.
  2. Bosscher D, Van Caille-Bertland M and Deelstra H. 2001. Effect of Thickening Agents, Based on Soluble Dietary Fiber, on Availability of Cacium, Iron and Zinc from Infant Formulas. Nutrition 17, 614. https://doi.org/10.1016/S0899-9007(01)00541-X
  3. Bougle D, Boudey M, Arban D, Bureau F, Neuville D and Orosdowsky M. 1996. In Vivo Study of The Absorption of Seaweed Minerals by Perfused Rat Intestine. Short Communication. Phytother Res 10. 325-326. https://doi.org/10.1002/(SICI)1099-1573(199606)10:4<325::AID-PTR820>3.0.CO;2-W
  4. Carlisle EM. 1986. Silicon as an Essential Trace Element in Animal Nutrition In: Silicon Biochemistry. Ciba Foundation Symposium 121, 123-139
  5. Cho DM, Kim DS, Lee DS, Kim HR and Ryeun JH. 1995. Trace Components and Functional Saccharides in Seaweed-1:Change in Proximate Composition and Trace Elements According to The Harvest Season and Places. Bull Kor Fish Soc 29, 49-59.
  6. Dorota PJ and Danuta Z. 1998. Osteocalcin as a Biochemical Marker of Bone Turnover. Review. Nephrology 4, 339-346. https://doi.org/10.1111/j.1440-1797.1998.tb00369.x
  7. Fuchs GJ, Farris RP and Deweir M. 1993. Iron Status and Intake of Older Infants Fed Formula vs Milk with Cereal. Am J Clin Nutr 58, 343.
  8. Heaney RP, Weaver CM and Fitzsimmons ML. 1990. Influence of Calcium Load on Absorption Fraction. J Bone Mineral Research 5, 1135-1138.
  9. Jeong HK, Kim JY and Lee HS. 1997. The Effect of Dietary Calcium and Phosphatate Levels on Calcium and Bone Metabolism in Rat. Kor Nutr Soc 30,813-824.
  10. Kawamura H, Ito A, Muramatsu T, Miyakawa S, Ochiai N and Tateishi T. 2003. Long-Term Implantation of Zinc-Releasing Calcium Phosphate Ceramics in Rabbit Femora. J Biomed Master. Res 67A, 468-674.
  11. Koba T, Matsui T and Yano H. 2001. Effect of Calcium Carbonate Exes on Some Mineral Metabolism in Young Rats. J Jap Soc Magnesium Res 20, 11-20.
  12. Korea Centers for Disease Control and Prevention (KCDCP). 2008. 2007 National Health Statistics-National Diet and Nutrition Survey. Seoul, Korea,
  13. Kumar R. 1995. Calcium Transport in Epitelial Cells of The Intestine and Kidney. J Cell Biochem 57, 392-398. https://doi.org/10.1002/jcb.240570304
  14. Kwak YH, Bai SC and Kim DJ. 2010. Estimated Availability and Major Minerals (Ca, P and Mg) Contents Bound Neutral Detergent Fiber (NDF) of Seaweeds. J Kor Soc Food Sci Nutr 39, 1073-1077. https://doi.org/10.3746/jkfn.2010.39.7.1073
  15. Lee CK, Choi JS, Jeong YJ, Byun HG and Kim SK. 1997. The Properties of Natural Hydroxyapatite Isolated from Tuna Bone. Bull Kor Fish Soc 30, 652-659.
  16. Lee JG, Lim YS, Joo DS and Jeong IH. 2002. Effects of Diet with Sea Tangle (Kjellemaniella Crassifolia) an Calcium Absorption and Feces in Rats. J Kor Fish Soc 35, 601-607. https://doi.org/10.5657/kfas.2002.35.6.601
  17. Levrat, MA, Remesy, C and Demigne, C, 1991, High Propionic Acid Fermentations and Mineral Accumulation in the Cecum of Rats Adapted to Different Levels of Inulin, J Nutr 121, 11, 1730-1737.
  18. Medeiros DM, Stoecker B, Plattner A, Jennings D and Haub M. 2004. Iron Deficiency Negatively Affects Vertebrae and Femurs of Rats Independently of Energy Intake and Body Weight. J Nutr 134, 3061-3067.
  19. Mitruka BM and Rawnsley HM. 1981. Clinical Biochemical and Hematological Reference Value in Normal Experimental Animals and Normal Humans. 2ed, Masson Pub., New York, U.S.A., 160.
  20. Miura T, Matsuzaki H, Suzuki K and Goto S. 1999. Long-Term High Intake of Calcium Reduces Magnesium Utilization in Rats. Nutr Res 19, 1363-1369. https://doi.org/10.1016/S0271-5317(99)00093-7
  21. Reeves PG, Nielsen FH and Fahey GC. Jr. 1993. AIN-93 Purified Diets for Laboratory Rodents: Final Report of The American Institute of Nutrition ad Hoc Writing Committee on The reformulation of the AIN-76A Rodent Diet. J Nutr 123, 1939-1951.
  22. Reinhart GA and Mahan DC. 1986. Effect of Various Calcium, Phosphorus Ratio at Low and High Dietary Phosphorus for Starter, Grower and Finishing Swine. J Animal Sci 63, 457-466. https://doi.org/10.2527/jas1986.632457x
  23. Ruperez P. 2002. Mineral Content of Edible Marine Seaweed. Food Chem 79, 23-26. https://doi.org/10.1016/S0308-8146(02)00171-1
  24. Uchiyama S, Hashizume M, Hokari Y, Nakagawa T, Igarashi A and Yamaguchi M. 2004. Characterization of Active Component in Marine Alga Sargassum honeri Extrat in Stimulating Bone Calcification In Vitro. J. Health Sci 50, 634-639. https://doi.org/10.1248/jhs.50.634
  25. Weaver CM. 2000. The growing Years and Prevention of Osteoporosis in Late Life. Proceedings of The Nutrition Society 59, 303-306. https://doi.org/10.1017/S0029665100000331
  26. Yamaguchi M, Hachiya S, Hiratsuka S and Suzuki T. 2001. Effect of Marine Algae Extract on Bone Calcification in the Femoral-Metaphyseal Tissues of Rats: Anabolic Effect of Sargassum honeri. J Health Sci 47, 533-538. https://doi.org/10.1248/jhs.47.533
  27. Ynsa MD. Ager FJ, Alvess LC, Zubeldia MA, Millan JC and Pinheiro T. 2006. Elemental Distributions in Femoral Bone of Rat under Osteoporosis Preventive Treatments. J Microscopy 224, 298-305. https://doi.org/10.1111/j.1365-2818.2006.01705.x