Effects of Arginine Supplementation on Bone Mineral Density and Bone Markers in OVX Rats

난소절제쥐에서 Arginine 첨가 식이가 골밀도 및 골대사에 미치는 영향

  • Choi, Mi-Ja (Department of Food and Nutrition, Keimyung University)
  • Published : 2009.06.30

Abstract

As far as we know, there were no studies of the effect of L-arginine on bone metabolism in post-menopausal women or ovariectomized rats. The primary objective of the current study was to determine whether arginine supplementation was associated with alterations in femoral and spinal bone mineral density (BMD) and bone markers in ovariectomized (Ovx) rats. Forty female Sprague-Dawley rats were divided into two groups, Ovx and sham groups, which were each randomly divided into two subgroups that were fed control and arginine supplemented diet. All rats were fed on experimental diet and deionized water ad libitum for 9 weeks. Bone formation was measured by serum osteocalcin and alkaline phosphatase (ALP) concentrations. Bone resorption was measured by deoxypyridinoline (DPD) crosslinks immunoassay and corrected for creatinine. Serum osteocalcin, growth hormone, insulin-like growth factor-1 (IGF-1), parathyroid hormone (PTH) and calcitonin were analyzed using radioimmunoassay kits. Bone mineral density (BMD) and bone mineral content (BMC) were measured using PIXImus (GE Lunar Co, Wisconsin, USA) in spine and femur. The serum and urine concentrations of Ca and P were determined. The plasma was analyzed for arginine. Diet did not affect weight gain, mean food intake, and plasma arginine concentration. Urinary Ca excretion was decreased by arginine supplementation in Ovx rats, but statistically not significant. The Ovx rats fed arginine-supplemented diet were not significantly different in ALP, osteocalcin, crosslinks value, PTH, calcitonin and IGF-1 compared to those fed control diet. The arginine-supplemented group had significantly higher serum Ca and growth hormone than control group. Spine and femur BMD were significantly increased by arginine supplementation on 5th and 9th weeks after feeding. Our findings indicate that dietary L-arginine supplementation decreased bone mineral density loss in Ovx rats. Therefore, dietary arginine supplementation may represent a potentially useful strategy for the management of osteoporosis.

Keywords

References

  1. Greendale GA, FitzGerald G, Huang MH, Sternfeld B, Gold E, Seeman T, Sherman S, Sowers M. Dietary soy isoflavones and bone mineral density: results from the study of women’s health across the nation. Am J Epidemiol 2002; 155(8): 746-754 https://doi.org/10.1093/aje/155.8.746
  2. Ho SC, Chan SG, Yi Q, Wong E, Leung PC. Soy intake and the maintenance of peak bone mass in Hong Kong Chinese women. J Bone Miner Res 2001; 16: 1363-1369 https://doi.org/10.1359/jbmr.2001.16.7.1363
  3. Setchell, KD, Lydeking-Olsen E. Dietary phytoestrogens and their effect on bone: evidence from in vitro and in vivo, human observational, and dietary intervention studies. Am J Clin Nutr 2003; 78: 593S-609S
  4. Atkinson C, Compston JE, Day NE, Dowsett M, Bingham SA. The effects of phytoestrogen isoflavones on bone density in women: a double-blind, randomized, placebo-controlled trial. Am J Clin Nutr 2004; 79: 326-333
  5. Spence LA, Lipscomb ER, Cadogan J, Martin B, Wastney ME, Peacock M, Weaver CM. The effect of soy protein and soy isoflavones on calcium metabolism in postmenopausal women: a randomized crossover study. Am J Clin Nutr 2005; 81: 916-922
  6. Andreassen TT, Jorgensen PH, Flyvbjerg A, Orskov H, Oxlund H. Growth hormone stimulates bone formation and strength of cortical bone in aged rats. J Bone Miner Res 1995; 10: 1057-1067 https://doi.org/10.1002/jbmr.5650100710
  7. Monson JP, Arake WM, Carroll PV, Weaver JU, Rodriguez- Arnao J, Savage MO. Influence of growth hormone on accretion of bone mass. Horm Res 2000; 58(Suppl)1: 52s-56s https://doi.org/10.1159/000064765
  8. Sugimoto T, Kaji H, Nakaoka D, Yamauchi M, Tano S, Sugishita T, Baylink DJ, Mohan S, Chihara K. Effect of low-dose of recombinant human growth hormone on bone metabolism in elderly women with osteoporosis. Eur J Endocrinol 2002; 147(3): 339-348 https://doi.org/10.1530/eje.0.1470339
  9. Choi MJ. Effects of arginine supplementation on bone mineral density in growing female rats. Korean J Nutr 2007; 40(3): 235- 241
  10. Reeves PG, Nielsen FH, Fahey GC. AIN-93 purified diets for laboratory rodents. J Nutr 1993; 123: 1939-1951
  11. Xing S, Cekan SZ, Dicafalusy U. Validation of radioimunoassay for estadiol-17 isotope dilution-mass spectrometry and a test of radiochemical purity. Clin Chem Acta 1983; 135: 189-201 https://doi.org/10.1016/0009-8981(83)90135-3
  12. Guarnero P, Grimaux M, Seguin P, Delmas P. Characterization of immunoreactive forms of human osteocalcin generated in vivo and in vitro. J Bone Min Res 1994; 9: 692-698 https://doi.org/10.1002/jbmr.5650090215
  13. Nanda N, Joshi H, Subbarao SK, Sharma VP. Two-site immunoradiometric assay (IRMA): detection, efficiency, and procedural modifications. J Am Mosq Control Assoc 1994; 10: 225-227
  14. Guarnero P, Grimaux M, Seguin P, Delmas P. Characterization of immunoreactive forms of human osteocalcin generated in vivo and in vitro. J Bone Min Res 1994; 9: 692-698 https://doi.org/10.1002/jbmr.5650090215
  15. Yvette C. Luiking and Nicolaas E. P. Deutz. Biomarkers of arginine and lysine excess. J Nutr 2007; 137: 1662S-1666S
  16. Daly JM, Reynolds J, Thom A, Kinsley L, Dietrick-Gallagher M, Shou J, Ruggieri B. Immune and metabolic effects of arginine in the surgical patient. Ann Surg 1988; 208: 512-523 https://doi.org/10.1097/00000658-198810000-00013
  17. Chyun JH, Griminger P. Improvement of nitrogen retention by arginine and glycine supplementation and its relation to collagen synthesis in traumatized mature and aged rats. J Nutr 1984; 114: 1697-1704
  18. Kohli R, Meininger CJ, Haynes TE, Yan W, Self JT, Wu G. Dietary L-arginine supplementation enhances endothelial nitric oxide synthesis in streptozotocin-induced diabetic rats. J Nutr 2004; 134(3): 600-608
  19. Mituka BM, Rawnsley HN. Clinical biochemical and hematological reference value in normal experimental animals and normal humans. 2nd edition, New York: Masson; 1987. p.160
  20. Choi MJ. Effects of soy protein on bone mineral content and bone mineral density in growing male rats. Korean J Nutr 2002; 35 (4): 409-413
  21. Choi MJ, Jo HJ. Effects of soy protein and isoflavones on bone mineral density in growing female rats. Korean J Nutr 2003; 36 (4): 359-367
  22. Choi MJ, Jung SH. The effect of dietary source and sulfur amino acid content on bone metabolism in growing rats. Korean J Nutr 2004; 37(2): 100-107
  23. Choi MJ. Effects of soy and isoflavones on bone markers and hormones in growing male rats. Korean J Nutr 2003; 36(5): 452- 458
  24. Choi MJ, Kim JH, Chang KJ. The effect of dietary taurine supplementation on plasma and liver lipid concentrations and free amino acid concentrations in rats fed a high-cholesterol diet. Adv Exp Med Biol 2006; 583: 235-242 https://doi.org/10.1007/978-0-387-33504-9_25
  25. Lee YM, Choi MJ, Chang KJ. The effect of dietary taurine supplementation on plasma and urinary free amino acid concentrations in diabetic rats. Adv Exp Med Biol 2003; 526: 75-82
  26. Choi MJ. Effects of soy and isoflavones on bone markers and hormones in growing male rats. Korean J Nutr 2003; 36(5): 452-458
  27. Kalu DN, Masoro EJ, Yu BP, Hardin RR, Hollis BW. Modulation of age related hyperparathyroidism and senile bone loss in fischer rats by soy protein and food restriction. Endocrinology 1998; 122: 1847-1854 https://doi.org/10.1210/endo-122-5-1847
  28. Choi MJ, Cho HJ. Effects of soy and isoflavones on bone metabolism in growing female rats. Korean J Nutr 2003; 36(6): 549- 558
  29. Bravenboer N, Hoizmann PJ, Matten JC, Stuurman LM, Roos JC, Lips P. Effect of long-term growth hormone treatment on bone mass and bone metabolism in growth hormone-deficient men. J Bone Miner Res 2005; 20(10): 1778-1784 https://doi.org/10.1359/JBMR.050613
  30. Dean HJ, Kellett JG, Bala RM. The effect of growth hormone treatment on somatomedin levels in growth hormone deficient children. J Clin Endocrinol Metab 1982; 55: 1167-1173 https://doi.org/10.1210/jcem-55-6-1167
  31. Lely AJ. Growth hormone and aging. GH & IGF Res 1999; 9: 117-119 https://doi.org/10.1016/S1096-6374(99)80023-9
  32. Lewinson D, Shenzer P, Hochberg Z. Growth hormone involvement in the regulation of tartrate resistant acid phosphatase positive cells that are active in cartilage and bone resorption. Calcif Tissue Int 1993; 52: 216-221 https://doi.org/10.1007/BF00298722
  33. Choi MJ. Effects of arginine supplementation on bone markers and hormones in growing female rats. Korean J Nutr 2007; 40 (4): 320-326
  34. Barret-Connor E, Goodman-Gruen D. Gender differences in insulin- like growth factor and bone mineral density association in old age: the Rancho Bernardo Study. J Bone Miner Res 1998; 13 (8): 1343-1349 https://doi.org/10.1359/jbmr.1998.13.8.1343
  35. Sugimoto T, Nishiyama K, Kuribayashi F, Chihara K. Serum levels of insulin-like growth factor (IGF) I, IGF binding protein (IGFBP)-2 and IGFBP-3 in osteoporotic patients with and without spinal fractures. J Bone Miner Res 1997; 12: 1272-1279 https://doi.org/10.1359/jbmr.1997.12.8.1272
  36. Krassas GE, Papadopoulou PH, Koliakos G. Growth hormone, insulin growth factor-I, and IGF binding protein-3 axis relationship with bone mineral density among healthy men. Arch Androl 2003; 49: 191-199 https://doi.org/10.1080/01485010390196724