칼슘과 제니스테인 섭취가 고지방식이로 유도된 비만 모델 마우스의 체지방과 지질대사에 미치는 영향

Effects of Calcium and Genistein on Body Fat and Lipid Metabolism in High Fat-induced Obese Mice

  • 김미현 (서울대학교 생활과학대학 식품영양학과, 생활과학연구소) ;
  • 김설희 (서울대학교 생활과학대학 식품영양학과, 생활과학연구소) ;
  • 박현우 (아모레퍼시픽 기술연구원 식품연구소 건강식품연구팀) ;
  • 김완기 (아모레퍼시픽 기술연구원 식품연구소 건강식품연구팀) ;
  • 이연숙 (서울대학교 생활과학대학 식품영양학과, 생활과학연구소)
  • Kim, Mi-Hyun (Department of Food & Nutrition, Research Institute of Human Ecology, Seoul Notional University) ;
  • Kim, Seol-Hee (Department of Food & Nutrition, Research Institute of Human Ecology, Seoul Notional University) ;
  • Park, Hyun-Woo (Health Product Research Team, Food Research Institute, Amorepacific Corporation R & D Center) ;
  • Kim, Wan-Gi (Health Product Research Team, Food Research Institute, Amorepacific Corporation R & D Center) ;
  • Lee, Yeon-Sook (Department of Food & Nutrition, Research Institute of Human Ecology, Seoul Notional University)
  • 발행 : 2006.12.31

초록

The study was conducted to investigate the effects of dietary calcium and soy isoflavone on body fat and lipid metabolism in high fat-induced obesity. Four week old female C57/BL6J mice, known as a good model of diet-induced obesity, were fed low Ca and high fat diet for 6 weeks. After induced obesity, mice were divided into six groups according to diets varying calcium contents (0.1 or 1.5%) and genistein contents (0 or 500 or 1,000 ppm). Body weight, fat pad (perirenal fat and parameterial fat), adipocyte size, serum total lipid and total cholesterol were significantly decreased by both high Ca intake and genistein supplementation. However, the effect of genistein supplementation showed in low Ca-fed groups. Serum LDL-cholesterol and TG were significantly decreased by high Ca intake and genistein supplementation, respectively. In liver, lipogenic enzymes (fatty acid synthase and malic enzyme) activity and TG were significantly decreased by both high Ca intake and genistein supplementation. This inhibitory effect of genistein on lipogenic enzymes showed in low Ca-fed groups. But liver total cholesterol and total lipid were significantly decreased by high Ca intake and genistein supplementation, respectively. Fecal excretion of total lipid, total cholesterol and TG were significantly increased by high Ca intake, not by genistein supplementation. In conclusion, high calcium intake and genistein supplement may be beneficial for suppression of obesity through direct anti-adipogenesis by decreasing fat weight and size and indirect anti-lipo-genesis by inhibiting lipogenic enzymes activity and improving lipid profile.

키워드

참고문헌

  1. James PT. Obesity: The worldwide epidemic. Clin Dermatol 22 (4): 276-280, 2004 https://doi.org/10.1016/j.clindermatol.2004.01.010
  2. National Health and Nutrition Survey, Ministry of Health and Welfare, Seoul, 2001
  3. Jacqmain M, Doucet E, Despres JP, Bouchard C, Tremblay A. Calcium intake, body composition, and lipoprotein-lipid concentrations in adults. Am J Clin Nutr 77(6):1448-1452, 2003 https://doi.org/10.1093/ajcn/77.6.1448
  4. Zemel MB, Shi H, Greer B, DiRienzo D, Zemel PC. Regulation of adiposity by dietary calcium. FASEB J 14: 1132-1138, 2000 https://doi.org/10.1096/fasebj.14.9.1132
  5. Watanabe S, Uesugi S, Kikuchi Y. Isoflavones for prevention of cancer, cardiovascular diseases, gynecological problems and possible immune potentiation. Biomed Pharm 56(6):302-312, 2002 https://doi.org/10.1016/S0753-3322(02)00182-8
  6. Naaz A, Yellayi S, Zakroczymski MA, Bunick D, Doerge DR, Lubahn DB, Helferich WG, Cooke PS. The soy isoflavone genistein decreases adipoase deposition in mice. Endocrinology 144: 3315-3320, 2003 https://doi.org/10.1210/en.2003-0076
  7. Goodman-Gruen D, Kritz-Silverstein D. Usual dietary isoflavone intake and body composition in postmenopausal women. Menopause 10(5): 427-432, 2003 https://doi.org/10.1097/01.GME.0000058866.35869.B4
  8. Lee YM, Choi JS, Kim MH, Jung MH, Lee YS, Song JH. Effects of dietary genistein on hepatic lipid metabolism and mitochondrial function in mice fed high-fat diet. J Nutr 22: 956-964, 2006 https://doi.org/10.1016/j.nut.2005.12.014
  9. Frings CS, Dunn RT. The colorimetric method for determination of serum total lipids based on the sulfo-phosphovanilin reaction. Am J Clin Pathol 52: 89-91, 1970
  10. Friedwald WT. Levy RI, Fredrickson DS. Estimation of the concentration of low density lipoprotein cholesterol in plasma without use of the preparative ultracentrifugation. Clin Chem 18: 499-502, 1972
  11. Folch J, Less M, Stanley GHS. A Simple method foy the isolation and purification of total lipids from animal tissues. J Biol Chem 226: 497-502, 1957
  12. Ashton AR. NADP-malic enzyme from C4 plant Flaveria bidents: Nucleotide substrate specificity. Arch Biochem Biophys 345: 251-258, 1997 https://doi.org/10.1006/abbi.1997.0260
  13. Linn TC. Purification and crystallization of rat liver fatty acid synthetase. Arch Biochem Biophys 209(2): 613-619, 1981 https://doi.org/10.1016/0003-9861(81)90320-9
  14. Lee JH, Lee YS. Effect of excess calcium and iron supplement on bone loss, nephrocalcinosis and renal function in osteoporotic model rats. Korean J Nutrition 33(2): 147-158, 2000
  15. Jenkins DJ, Kendall CW, Jackson CJ, Connelly PW, Parker T, Faulkner D, Vidgen E, Cunnane SC, Leiter LA, Josse RG. Effects of high- and low- isoflavone soyfoods on blood lipids, oxidized LDL, homocystein, and blood pressure in hyperlipidemic men and women. Am J Clin Nutr 76: 365-372, 2002 https://doi.org/10.1093/ajcn/76.2.365
  16. Reid IR, Mason B, Horne A, Ames R, Clearwater J, Bava U, Orr- Walker B, Wu F, Evans MC, Gamble GD. Effects of calcium supplementation on serum lipid concentrations in normal older women: a randomized controlled trial. Am J Med 112(5): 343-347, 2002 https://doi.org/10.1016/S0002-9343(01)01138-X
  17. Lee YS, Shin DM. Effect of dietary calcium and sodium level on lipid metabolism in hyperlipidemic/hypercholesterolemic rats. Korean J Nutrition 33(4): 403-410, 2000
  18. Denke MA, Fox MM, Schulte MC. Short-term dietary calcium fortification increases fecal saturated fat content and reduces serum lipids in men. J Nutr 123(6): 1047-1053, 1993
  19. Kirk EA, Sutherland P, Wang SA, Chait A, LeBoeuf RC. Dietary isoflavones reduce plasma cholesterol and atherosclerosis in C57BL/6 mice but not LDL receptor-deficient mice. J Nutr 128 (6): 954-959, 1998 https://doi.org/10.1093/jn/128.6.954
  20. Kawakami Y, Tsurugasaki W, Yoshida Y, Igarashi Y, Nakamura S, Osada K. Regulative actions of dietary soy isoflavone on biological antioxidative system and lipid metabolism in rats. J Agric Food Chem 52(6): 1764-1768, 2004 https://doi.org/10.1021/jf0345898
  21. Sood A, Harold LS, Jack HO. Tissue-Specific Regulation of Malic Enzyme by Thyroid Hormone in the Neonatal Rat. Biochem Biophys Res Commun 22(2): 287-291, 1996
  22. Divi RL, Chang HC, Doerge DR. Anti-Thyroid Isoflavones from Soybean. Biochem Pharmacol 54(10): 1087-1096, 1997 https://doi.org/10.1016/S0006-2952(97)00301-8
  23. Schmutzler C, Inka H, Peter JH, Gabor K, Luise S, Birgit M, Lutz S, Petra A, Annetic G, Dana S. Endocrine active compounds affect thyrotropin and thyroid hormone level in serum as well as endpoints of thyroid hormone action in liver, heart and kidney. Toxicology 205: 95-102, 2004 https://doi.org/10.1016/j.tox.2004.06.041
  24. Zemel MB. Regulation of adiposity and obesity risk by dietary calcium: mechanisms and implications. J Am Coll Nutr 21(2): 146S-151S, 2002
  25. Xue B, Zemel MB. Relationship between human adipose tissue agouti and fatty acid synthase (FAS). J Nutr 130(10): 2478-2481, 2000 https://doi.org/10.1093/jn/130.10.2478
  26. Brusselmans K, Vrolix R, Verhoeven G, Swinnen JV. Induction of cancer cell apoptosis by flavonoids is associated with their ability to inhibit fatty acid synthase activity. J Biol Chem 1-29, 2004
  27. Heim M, Frank O, Kampmann G, Sochocky N, Pennimpede T, Fuchs P, Hunziker W, Weber P, Martin I, Bendik I. The phytoestrogen genistein enhances osteogenesis and represses adipogenic differentiation of human primary bone marrow stromal cells. Endocrinology 145(2): 848-859, 2004 https://doi.org/10.1210/en.2003-1014