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Combined effects of oral oleoyl-estrone and limited food intake on body composition of young overweight male rats

Abstract

Objective:

The combined effects of limited food intake and OE treatment have been analysed in order to determine whether hypocaloric diets enhance the slimming effects of OE on mature overweight male rats. Two levels of dietary limitation at 50 and 25% of a standard intake were established, roughly corresponding to the human LCDs and VLCDs.

Design:

Wistar male rats (6 weeks old) were made overweight by a cafeteria diet. After transition to standard diet, they were subjected to food restriction: down to 50 or 25% with respect to the transition period. Half the animals were given daily oral gavages of 10 nmol/g oleoyl-estrone (OE), and the rest received only the vehicle during 10 days.

Measurements:

Changes in weight and body composition: water, lipid, protein or gross energy were determined by comparing the final pool size with that of day 0, calculated from the initial body weight and the composition of untreated rats. Energy and nitrogen balances were estimated. Plasma levels of metabolites and hormones were also measured.

Results:

OE induced changes in body composition similar to those elicited by a 50% reduction in food, with massive loss of lipid and energy. OE-treated rats ate less than the controls, but additional effects on body composition on reduced diet were minimal. OE improved metabolic homoeostasis: better maintained glycaemia, lower cholesterol and shallower hormonal changes, but at the expense of slightly increased protein mobilisation.

Conclusions:

The data presented suggest that no advantages are accomplished by combining OE treatment and hypocaloric diets compared with OE alone, at least under the experimental conditions tested, since the effects were not additive. Despite OE affecting food intake, mechanisms other than that are deemed responsible for the mobilisation of body fat, since intake alone cannot explain the effects on body weight, nor the metabolic and hormonal changes in OE-treated rats. It is concluded that the combination of food restriction and OE may result in unwanted increased protein mobilisation with no synergy between both slimming treatments.

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References

  1. Cahill GF, Herrera MG, Morgan AP, Soeldner J, Steinke J, Levy PL et al. Hormone fuel relationships during fasting. J Clin Invest 1966; 45: 1751–1769.

    Article  CAS  Google Scholar 

  2. Felig P, Owen OE, Wahren J, Cahill GF . Amino acid metabolism during prolonged starvation. J Clin Invest 1969; 48: 584–594.

    Article  CAS  Google Scholar 

  3. Palou A, Remesar X, Arola L, Herrera E, Alemany M . Metabolic effects of short term food deprivation in the rat. Horm Metabol Res 1981; 13: 326–330.

    Article  CAS  Google Scholar 

  4. Santos Pinto FN, Luz J, Griggio MA . Energy expenditure of rats subjected to long-term food restriction. Int J Food Sci Nutr 2001; 52: 193–200.

    Article  CAS  Google Scholar 

  5. Sanchis D, Balada F, Grasa MM, Virgili J, Peinado J, Monserrat C et al. Oleoyl-estrone induces the loss of body fat in rats. Int J Obes Relat Metab Disord 1996; 20: 588–594.

    CAS  Google Scholar 

  6. Virgili J, Casals I, Peinado-Onsurbe J, Esteve M, Julve J, Fernández-López JA et al. Distribution of oleoyl-estrone in rat plasma lipoproteins. Horm Metab Res 1999; 31: 597–601.

    Article  CAS  Google Scholar 

  7. Balada F, Sanchis D, Virgili J, Grasa MM, Monserrat C, Fernández-López JA et al. Effect of the slimming agent oleoyl-estrone in liposomes (Merlin-2) on the body weight of rats fed a cafeteria diet. Arch Physiol Biochem 1997; 105: 487–495.

    Article  CAS  Google Scholar 

  8. Grasa MM, Vilà R, Esteve M, Cabot C, Fernández-López JA, Remesar X et al. Oleoyl-estrone lowers the body weight of both ob/ob and db/db mice. Horm Metab Res 2000; 32: 246–250.

    Article  CAS  Google Scholar 

  9. Sanchis D, Balada F, Picó C, Grasa MM, Virgili J, Farrerons C et al. Rats receiving the slimming agent oleoyl-estrone in liposomes (Merlin-2) decrease food intake but maintain thermogenesis. Arch Physiol Biochem 1997; 105: 663–672.

    Article  CAS  Google Scholar 

  10. Sanchis D, Adán C, Ardévol A, Grasa MM, Cabot C, Balada F et al. Short-term treatment with oleoyl-estrone in liposomes (Merlin-2) strongly reduces the expression of the ob gene in young rats. Biochem J 1997; 326: 357–360.

    Article  CAS  Google Scholar 

  11. Grasa MM, Cabot C, Esteve M, Yubero P, Masanés RM, Blay M et al. Daily oral oleoyl-estrone gavage induces a dose-dependent loss of fat in Wistar rats. Obes Res 2001; 9: 202–209.

    Article  CAS  Google Scholar 

  12. Cabot C, Salas A, Ferrer-Lorente R, Savall P, Remesar X, Fernández-López JA et al. Short-term oral oleoyl-estrone treatment increases plasma cholesterol turnover in the rat. Int J Obes Relat Metab Disord 2005; 29: 534–539.

    Article  CAS  Google Scholar 

  13. Blay M, Peinado-Onsurbe J, Grasa MM, Díaz-Silva M, Fernández-López JA, Remesar X et al. Effect of oral oleoyl-estrone treatment on plasma lipoproteins and tissue lipase and lipase activities of Zucker lean and obese female rats. Int J Obes Relat Metab Disord 2002; 26: 618–626.

    Article  CAS  Google Scholar 

  14. van Gaal LF, Vansant GA, de Leeuw IH . Factors determining energy expenditure during very-low-calorie diets. Am J Clin Nutr 1992; 56 (Suppl 1): 224S–229S.

    Article  CAS  Google Scholar 

  15. Dulloo AG, Girardier L . Influence of dietary-composition on energy-expenditure during recovery of body-weight in the rat – Implications for catch-up growth and obesity relapse. Metabolism 1992; 41: 1336–1342.

    Article  CAS  Google Scholar 

  16. Ryan DH . Clinical use of sibutramine. Drugs Today 2004; 40: 41–54.

    Article  CAS  Google Scholar 

  17. López-Martí J, Díaz -Silva M, Salas A, Grasa MM, Fernández-López JA, Remesar X et al. Oleoyl-estrone induces the massive loss of body weight in Zucker fa/fa rats fed a high-energy hyperlipidic diet. J Nutr Biochem 2000; 11: 530–535.

    Article  Google Scholar 

  18. Remesar X, Guijarro P, Torregrosa C, Grasa MM, López J, Fernández-López JA et al. Oral oleoyl-estrone induces the rapid loss of body fat in Zucker lean rats fed a hyperlipidic diet. Int J Obes Relat Metab Disord 2000; 24: 1405–1412.

    Article  CAS  Google Scholar 

  19. Alemany M, Fernández-López JA, Petrobelli A, Granada M, Foz M, Remesar X . Pérdida de peso en un paciente con obesidad mórbida en tratamiento con oleoil-estrona. Med Clin (Barc) 2003; 121: 496–499.

    Article  Google Scholar 

  20. Ferrer-Lorente R, Cabot C, Fernández-López JA, Remesar X, Alemany M . Effects of oleoyl-estrone with dexfenfluramine, sibutramine or phentermine on overweight rats. Eur J Pharmacol 2005; 513: 243–248.

    Article  CAS  Google Scholar 

  21. Rafecas I, Esteve M, Fernández-López JA, Remesar X, Alemany M . Whole rat protein content estimation: applicability to the Nx6.25 method. Br J Nutr 1994; 72: 199–209.

    Article  CAS  Google Scholar 

  22. Folch J, Lees M, Sloane-Stanley GH . A simple method for the isolation and purification of total lipids from animal tissues. J Biol Chem 1957; 232: 497–509.

    Google Scholar 

  23. Esteve M, Rafecas I, Remesar X, Alemany M . Nitrogen balance discrepancy in Wistar rats fed a cafeteria diet. Biochem Int 1992; 26: 687–694.

    CAS  PubMed  Google Scholar 

  24. Matthews DR, Hosker JP, Rudenski AS, Naylor BA, Teacher DF, Turner RC . Homeostasis model assessment: insulin resistance and B cell function from fasting plasma glucose and insulin concentration in man. Diabetologia 1985; 28: 412–419.

    Article  CAS  Google Scholar 

  25. Bonora E, Saggiani F, Targher G, Zenere MB, Alberiche M, Monauni T et al. Homeostasis model assessment closely mirrors the glucose clamp technique in the assessment of insulin sensitivity. Studies in subjects with various degrees of glucose tolerance and insulin sensitivity. Diabet Care 2000; 23: 57–63.

    Article  CAS  Google Scholar 

  26. Díaz M, Grasa MM, Fernández-López JA, Remesar X, Alemany M . Short-term effects of oleoyl-estrone on insulin sensitivity and glucose disposal in the rat. Int J Obes Relat Metab Disord 2002; 26 (Suppl 1): S204 (abstract).

    Google Scholar 

  27. Felig P . The glucose-alanine cycle. Metabolism 1973; 21: 197–207.

    Google Scholar 

  28. Grasa MM, Díaz-Silva M, Fernández-López JA, Remesar X, Alemany M . Oleoyl-estrone decreases rat plasma insulin, leptin and adiponectin, lowering muscle and BAT glucose uptake. Int J Obes Relat Metab Disord 2003; 27, P1-001 (abstract).

  29. Cahill GF, Owen PE, Morgan AP . The consumption of fuels during prolonged starvation. Adv Enzyme Regul 1968; 6: 143–150.

    Article  CAS  Google Scholar 

  30. Considine RV, Sinha MK, Heiman ML, Kriauciunas A, Stephens TW, Nyce MR et al. Serum immunoreactive leptin concentrations in normal-weight and obese humans. N Engl J Med 1996; 334: 292–295.

    Article  CAS  Google Scholar 

  31. Weyer C, Funahashi T, Tanaka S, Hotta K, Matsuzawa Y, Pratley RE et al. Hypoadiponectinemia in obesity and type 2 diabetes: close association with insulin resistance and hyperinsulinemia. J Clin Endocr Metab 2001; 86: 1930–1935.

    Article  CAS  Google Scholar 

  32. Lihn AS, Pedersen SB, Richelsen B . Adiponectin: action, regulation and association to insulin sensitivity. Obes Rev 2005; 6: 13–21.

    Article  CAS  Google Scholar 

  33. Vendrell J, Broch M, Vilarrasa N, Molina A, Gómez JM, Gutiérrez C et al. Resistin, adiponectin, ghrelin, leptin, and proinflammatory cytokines: relationships in obesity. Obes Res 2004; 12: 962–971.

    Article  CAS  Google Scholar 

  34. Remesar X, Fernández-López JA, Blay MT, Savall P, Salas A, Díaz-Silva M et al. Effect of oral oleoyl-estrone on adipose tissue composition in male rats. Int J Obes Relat Metab Disord 2002; 26: 1092–1102.

    Article  CAS  Google Scholar 

  35. Salas A, Esteve M, Alemany M, Remesar X . Oleoyl-estrone induces apoptosis in different locations of rat white adipose tissue. Int J Obes Relat Metab Disord 2004; 28 (Suppl 1): S103 (abstract).

    Google Scholar 

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Acknowledgements

We thank CCN-IEC and Mercadona for their help in financing this project.

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Correspondence to M Alemany.

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Romero, M., Esteve, M. & Alemany, M. Combined effects of oral oleoyl-estrone and limited food intake on body composition of young overweight male rats. Int J Obes 30, 1149–1156 (2006). https://doi.org/10.1038/sj.ijo.0803224

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