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Oral oleoyl-estrone induces the rapid loss of body fat in Zucker lean rats fed a hyperlipidic diet

International Journal of Obesity volume 24, pages 1405–1412 (2000)Cite this article

Abstract

OBJECTIVE: To test whether oleoyl-estrone affects body weight when given orally, which may help curtail the secondary growth-boosting effects of derived estrone.

DESIGN: The rats were fed for 15 days with a powdered hyperlipidic diet (16.97 MJ/kg metabolizable energy) in which 46.6% was lipid-derived and 16.1% protein-derived energy (HL group), containing 1.23±0.39 μmol/kg of fatty-acyl esters of estrone. This diet was supplemented with additional oleoyl-estrone to produce diets with 2.5 μmol/kg (diet OE2.5), 4.4 μmol/kg (diet OE4.4), and 33.3 μmol/kg content in fatty-acyl estrone (diet OE33).

SUBJECTS: Twelve-week old female Zucker lean (Fa/?) rats initially weighing 200–235 g.

MEASUREMENTS: Food intake and body weight changes; urine and droppings production and nitrogen content. Body composition (water, lipid, protein) and total energy. Energy and nitrogen balances. Plasma chemistry including free amino acids.

RESULTS: Oral administration of oleoyl-estrone in a hyperlipidic diet resulted in significant losses of fat, energy and, ultimately, weight, which were dependent on the dose of oleoyl-estrone ingested. Treatment induced the maintenance of energy expenditure combined with lower food intake, creating an energy gap that was filled with internal fat stores whilst preserving body protein. The decrease in food intake was not a consequence of food aversion but of diminished appetite. Energy expenditure was practically constant for all groups except for the OE33, which showed values about 25% lower than the controls. In most of the groups studied, there was a net protein deposition in spite of severe lipid and energy drainage. Amino acid levels agreed with this N-sparing shift. In spite of lowered energy intake, the N balance was positive or near zero in all groups, with a sizeable N-gap in controls and in lower-dose groups that disappeared in the OE33 group.

CONCLUSION: Treatment of rats with a hyperlipidic diet containing added oleoyl-estrone resulted in the dose-related loss of fat reserves with scant modification of other metabolic parameters and preservation of body protein. The results agree with the postulated role of oleoyl-estrone as a ponderostat signal and open the way for its development as anti-obesity drug.

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Acknowledgements

This study was financed by Laboratoris SALVAT, SA. and grants ALI96-1094, BIO98-0316 and 2FD97-0233 of the Government of Spain. Thanks are given to Robin Rycroft from the Language Advisory Service at the University of Barcelona for correction of the text.

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  1. Centre de Recerca en Nutrició i Ciència dels Aliments, Universitat de Barcelona, Barcelona, Spain

    X Remesar, P Guijarro, C Torregrosa, MM Grasa, J López, JA Fernández-López & M Alemany

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  1. X Remesar
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Correspondence to M Alemany.

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Remesar, X., Guijarro, P., Torregrosa, C. et al. Oral oleoyl-estrone induces the rapid loss of body fat in Zucker lean rats fed a hyperlipidic diet. Int J Obes 24, 1405–1412 (2000). https://doi.org/10.1038/sj.ijo.0801393

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