The differences in metabolic responses between dietary orotate and adenine in lipid profiles of serum and liver tissues

Authors

  • Yohanes Buang

DOI:

https://doi.org/10.13181/mji.v19i4.409

Abstract

Aim: Objectives to evalate the differences in metabolic responses between dietary orotic acid and adenine in lipid profiles of serum and liver tissues.

Methods: Rats were paired-fed 1.0 % orotic acid (orotic acid group) and 0.25 % adenine (adenine group) diets or a non-supplemented diet (control group) for 10 days. Serum lipid concentrations were measured using enzyme assay kits. Lipids of liver tissues were extracted and the lipid contents were  determined.

Results: Serum lipid concentrations (in mg/dL) of adenine group tended to increase whereas those levels decreased in orotic acid group compared to control group. The serum triglyceride (TG) concentrations of control, orotic acid, and adenine groups were (78.1±14.9), (69.0±23.6), and (136.1±21.6); phospholipids (PL): (109.2±11.5), (93.3±10.5), and (131.3±11.0); total cholesterol: (53.7±4.6), (42.9±6.5), and (68.1±5.8); and high-density lipoprotein (HDL)-cholesterol: (35.4±2.7),(33.0±3.0), and (44.7±2.7), respectively. Furthermore, liver TG content of orotic acid group markedly increased. The increase was approximately by 10-fold in comparison to other groups (P<0.05). The lipid contents of liver tissues (in mg/g tissue) in ordinarily of those three groups for TG were (11.4±1.3), (123.5±15.2), and (11.9±1.2); PL: (27.1±0.8), (25.4±1.3), and (30.7±0.6); and the total cholesterol: (2.73±0.09), (2.34±0.12), and (2.91±0.08), respectively. The liver PL and cholesterol content of adenine group increased by 21% and 25% than that of orotic acid group, but both lipid levels of the latter group increased by 7% and 15%, respectively, than that of the control group.

Conclusion: Dietary adenine enhances the serum TG, PL, cholesterol, and HDL-cholesterol and the liver PL and cholesterol but without alters the liver TG levels. Dietary orotic acid, however, attenuates these serum lipid levels but retains those lipids  synthesized in liver cells, mainly TG. (Med J Indones 2010; 19:217-22)

Keywords: Adenine, liver lipids, lipogenesis, orotic acid, serum  lipids

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References

Salerno C, Crifo C. Diagnostic value of urinary orotic acid levels: applicable separation methods. J Chrom. B Analyt Technol Biomed Life Sci. 2002; 781:57-71. https://doi.org/10.1016/S1570-0232(02)00533-0

Vandamme EJ. Production of vitamins, coenzymes and related biochemicals by biotechnological processes. J Chem Technol Biotechnol. 1992; 53:313-27. https://doi.org/10.1002/jctb.280530402

Motyl T, Krzeminski J, Podgurniak M, Witeszczak C, Zochowski P. Variability of orotic acid concentration in cow's milk. Endocr Regul. 1991; 25:79-82.

Lehninger, Nelson, Cox. 1993, Principles of Biochemistry 2nd ed. Worth Publishers, Inc. USA.

Stipanuk MH. Biochemical, Physiological, and Molecular Aspects of Human Nutrition. 2nd Ed., 2006. Published by Saunders-Elsevier, New York: page 666-72.

Allen L, deBenoist B, Dary O. Guidelines on food fortifi cation with micronutrients. WHO Library Cata-loguing-in-Publication Data. 2006; 73-80.

Website http://ghr.nlm.nih.gov/ghr/glossary/adenine. Accessed July 10, 2009.

Pottenger LA, Gets GS. Serum lipoprotein accumulation in the livers orotic acid-fed rats. J lipid Res. 1971;12: 450-9. https://doi.org/10.1016/S0022-2275(20)39494-3

Buang Y, Wang YM, Cha JY, Nagao K, Yanagita T. Dietary phosphatidylcholine alleviates fatty liver induced by orotic acid. Nutrition. 2005; 21: 867-73. https://doi.org/10.1016/j.nut.2004.11.019

Buang Y, Cha JY, Nagao K, Wang YM, Inoue N, Yanagita T. Alleviation of fatty liver by a-linolenic acid. J Nutr Sci Vitaminol. 2004; 50: 272- 6. https://doi.org/10.3177/jnsv.50.272

Miyazawa S, Furuta S, Hashimoto T. Reduction of v-oxidation capacity of rat liver mitochondria by feeding orotic acid. Biochim. Biophys. Acta. 1982; 711: 494-502. https://doi.org/10.1016/0005-2760(82)90064-9

Cha JY, Cho YS, Kim I, Anno T, Rahman SM, Yanagita T. Effect of hesperetin, a citrus fl avonoid, on the liver triacylglycerol content and phosphatidate phosphohydrolase activity in orotic acid-fed rats. J Plant Foods Human Nutr. 2001;17:1-10.

Folch J, Lees M, Sloane-Starley GH. A simple method for the isolation and purifi cation of total lipids from animal tissues. J. Biol. Chem.1957; 226:497-509. https://doi.org/10.1016/S0021-9258(18)64849-5

Fletcher MM. A colorimetric method for estimating serum triglycerides. Clin. Chim. Acta. 1968; 22:393-7. https://doi.org/10.1016/0009-8981(68)90041-7

Barlett GR. Phosphorous assay in column chromatography. J. Biol. Chem.1959; 234: 466-8. https://doi.org/10.1016/S0021-9258(18)70226-3

Sperry WM, Webb M. A revision of the schoenheimer-sperry method for cholesterol determination. J. Biol. Chem. 1950;187: 97-106. https://doi.org/10.1016/S0021-9258(19)50934-6

Nagao K, Wang YM, Inoue N, Han SY, Buang Y, Noda T, et al. The 10trans, 12cis Isomer of Cunjugated Linoleic Acid Promotes Energy Metabolism in OLETF Rats. Nutrition. 2003; 19, 7-8: 652-6. https://doi.org/10.1016/S0899-9007(03)00060-1

Lowry OH, Rosebrough NJ. Farr AL. Randal RJ. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951;193: 265-75. https://doi.org/10.1016/S0021-9258(19)52451-6

Duncan DB. Multiple range and multiple F Test. Biometric. 1955;11: 1-42. https://doi.org/10.2307/3001478

Li Z, Clark J, Diehl AM. The liver in obesity and type 2 diabetes mellitus. Clin Liver Dis. 2002; 6: 867-77. https://doi.org/10.1016/S1089-3261(02)00060-0

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Published

2010-11-01

How to Cite

1.
Buang Y. The differences in metabolic responses between dietary orotate and adenine in lipid profiles of serum and liver tissues. Med J Indones [Internet]. 2010Nov.1 [cited 2024Nov.22];19(4):217-22. Available from: http://mji.ui.ac.id/journal/index.php/mji/article/view/409

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Basic Medical Research
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