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Effects of Water Extracts from Mulberry Leaves on Hepatic HMG-CoA Reductase and Acyl-CoA-Cholesterol Acyl Transferase Activity in Rats Fed High Cholesterol Diets

  • Choi, Jeong-Hwa (School of Food Science, Jinju International University) ;
  • Hong, Jung-Hee (Department of Food Science and Nutrition, Catholic University of Daegu) ;
  • Yang, Jeong-Ah (Department of Food Science and Nutrition, Catholic University of Daegu) ;
  • Rhee, Soon-Jae (Department of Food Science and Nutrition, Catholic University of Daegu) ;
  • Park, Mo-Ra (Department of Food Science and Nutrition, Sangju National University)
  • Published : 2006.03.01

Abstract

This study investigated the effects of mulberry leaf extract on lipid metabolism in rats fed a high cholesterol diet. Sprague-Dawley male rats weighing $100{\pm}10g$ were randomly assigned either to one of two normal diet groups, with (NE group) or without (N group) mulberry extract, or one of four high cholesterol groups containing 1% cholesterol and various levels of dietary mulberry leaf extract. The rats fed high cholesterol diets were subdivided into 4 groups according to level of mulberry extract; Mulberry extract free group (HC group), 0.8% mulberry leaf extract group (HCL group), 1.6% mulberry leaf extract (HCM group) and 3.2% mulberry leaf extract (HCH group). The rats were fed their respective diets ad libitum for 4 weeks. The levels of serum triglyceride, total cholesterol and LDL-cholesterol of the HC group were higher than mulberry leaf extract supplemented groups. In contrast, the levels of serum HDL-cholesterol in groups supplemented with mulberry leaf extract were significantly lower than that of HC group. Hepatic total lipids, triglycerides, and cholesterol were significantly higher in the high cholesterol groups compared to those of the normal group, but were lower in the HCL, HCM and HCH groups than in the HC group. HMG-CoA reductase activity was significantly decreased in the HC and HCL groups compared to the normal and NE groups. However, the activities in the HCM and HCH group were similar to that of the normal group. The activity of acyl-CoA-cholesterol acyl transferase (ACAT) was increased in high cholesterol groups compared to the normal group. However, the activity was lower for all of the high cholesterol groups fed mulberry leaf extracts, and was lowest for the highest supplemented group (HCH), with no significantly difference from the normal group. In conclusion, the reduction in serum and hepatic lipid composition by mulberry leaf extract may be due to its modulation of HMG-CoA reductase and ACAT activities.

Keywords

References

  1. Korea National Statistical Office. Population items. http:// kosis.nso.go.kr/ (accessed June 2003)
  2. Framingham Heart Study. http://www.nhlbi.nih.gov/ (accessed March 2005)
  3. Kim SY, GA JJ, Lee WC, Ryu KS, Lee KR, Kim YC. 1999. Antioxidative flavonoids from the leaves of Morus alba. Arch Pharm Res 22: 81-85 https://doi.org/10.1007/BF02976442
  4. Purusotam B, Shigetoshi K, Satoshi T, Mineo S, Tsuneo N. 1993. Two new 2-arylbenzofuran derivatives from hypoglycemic activity-bearing fractions of Morusinsignis. Chem Pharm Bull 41: 1238-1243 https://doi.org/10.1248/cpb.41.1238
  5. Massayasu K, Fu-jun C, Noboru N, Ikuho K, Naoki A, Sakuji K. 1995. Anti hyperglycemic effect of N-containing sugars delived from mulberry leaves in streptozotocin- induced diabetic mice. J Traditional Medicine 12: 214- 219
  6. Lee JS. 1994. Blood glucose lowering effect of SangYup (Mori Folium). MS Thesis. Kyung Hee University
  7. Kim SY, Lee WC, Kim HB, Kim SK. 1998. Antihyperlipidemic effects of methanol extracts from mulberry leaves in cholesterol induced hyperlipidemia in rats. J Korean Soc Food Sci Nutr 27: 1217-1222
  8. Yun SJ, Lee WC. 1994. Characteristics of superoxide dismutases of mulberry leaf. Korean J Breed 26: 389-393
  9. Hong JH, Park MR, Rhee SJ. 2002. Effects of YK-209 mulberry leaves on HMG CoA reductase and lipid com-position of liver in streptozotocin-induced diabetic rats. J Korean Soc Food Sci Nutr 31: 826-833 https://doi.org/10.3746/jkfn.2002.31.5.826
  10. Chae JY, Lee JY, Hoang IS, Whangbo D, Choi PW, Lee WC, Kim JW, Kim SY, Choi SW, Rhee SJ. 2003. Analysis of functional components of leaves of different mulberry cultivars. J Korean Soc Food Sci Nutr 32: 15-21 https://doi.org/10.3746/jkfn.2003.32.1.015
  11. Friedwald WT, Levy RI, Fedreicson DS. 1972. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without was of the preparative ultracentrifuge. Clin Chem 18: 499-506
  12. Fiordaliso M, Kok N, Desager KP, Goethals F, Deboyser D. 1977. Estimation of the concentration of low-density lipoprotein cholesterol in plasma. Am J Clin Nutr 30: 171 https://doi.org/10.1093/ajcn/30.2.171
  13. Folch JM, Lee M, Stanley GHS. 1957. A simple method for the isolation and purification of total lipids from animal tissue. J Biol Chem 26: 497-509
  14. Sale FD, Marchesini S, Fishman PH, Berra B. 1984. A sensitive enzymatic assay for determination of cholesterol in lipid extracts. Academic Press Inc, New York. p 347- 350
  15. Hulcher FH, Oleson WH. 1974. Simplified spectropho-tometric assay for microsomal 3-hydroxy-3-meth-ylglutaryl Co A reductase by measurement of coenzyme A. J Lipid Res 14: 625-632
  16. Shapiro DJ, Nordstrom JL, Mitschelen JJ, Rodwell VW, Schimke RT. 1974. Microassay for 3-hydroxy-3-meth-ylglutaryl Co A reductase in rat liver and in L-cell fibroblast. Biochim Biophy Acta 370: 369-377 https://doi.org/10.1016/0005-2744(74)90098-9
  17. Erickson SK, Schrewsbery MA, Brooks C, Meyer DJ. 1980. Rat liver acyl-coenzyme A:cholesterol acyltransferase: its regulation in vivo and some of properties in vitro. J  Lipid Res 21: 930-941
  18. Gillies PJ, Rathgeb KA, Robinson CS. 1986. Regulation of acyl-coenzyme A:cholesterol acyltransferase activity in normal and atherosclerotic rabbit aortas: Role of a cholesterol substrate pool. Exp Mol Pathol 44: 329-339 https://doi.org/10.1016/0014-4800(86)90046-8
  19. Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. 1951. Protein measurement with thefolin phenol. J Biol Chem 193: 265-275
  20. Lee WC, Kim AJ, Kim SY. 2003. The study on the functional materials and effects of mulberry leaf. Food Science and Industry 36(3): 2-13
  21. Do KM, Park YB, Bok SH, Lee MK, Jeong TS, Choi MS. 2001. Alteration of lipid metabolism by ginseng supplements with different levels of vitamin E in high cholesterol-fed rats. J Food Sci Nutr 6: 66-72
  22. Kim JH, Jeon SM, Park YA, Choi MS, Moon KD. 1999. Effects of safflower seed (Carthamus tinctorious L.) powder on lipid metabolism in high fat and high cholesterol- fed rats. J Korean Soc Food Sci Nutr 28: 625-631
  23. Choi MS, Bok SH. 2001. Comparison of jujube extract with tangerine peel extract in lowering lasma lipids and activities cholesterol regulating enzymes in cholesterol-fed rats. J Food Sci Nutr 6: 122-12
  24. Carr TP, Parks SJ, Rudel LL. 1992. Hepatic ACAT activity in African green monkeys is highly colerated to plasma LDL cholesteryl ester enrichment and coronary artery atherosclerosis. Arterioscler Thromb Vasc Biol 12: 1274- 1283 https://doi.org/10.1161/01.ATV.12.11.1274