Abstract
Background and aims:
As interleukin-6 (IL-6) has an important role in general metabolism with high circulating levels in obesity and other associated diseases, the factors regulating its synthesis and release have been considered possible therapeutic targets and have recently been studied. We examined the influence of three different diets, each having a different fatty acid composition—saturated, monounsaturated or polyunsaturated (coconut oil, olive oil and sunflower oil diets), on IL-6 release from rat adipocytes, and the interaction between diet and other regulatory factors of IL-6 release, such as epinephrine.
Methods:
A group of rats was assigned to one of the three different diets, each with a significantly different concentration of saturated, monounsaturated and polyunsaturated fatty acids. Samples were taken from the omental adipose tissue for measurement of the triacylglycerol fatty acid composition of the tissues and for adipocyte isolation. IL-6 release from adipocytes was measured in vitro, under nonstimulated conditions and also with two concentrations of epinephrine in the medium.
Results:
Animals fed with the olive oil diet showed lower values of IL-6 release with and without epinephrine stimulation. IL-6 release from adipocytes varied according to the diet, but not according to epinephrine dose. However, a significant interaction was found between the epinephrine dose and the diet in IL-6 release regulation.
Conclusions:
IL-6 release from adipocytes was markedly regulated by the dietary fatty acid composition, even under epinephrine stimulation, with lower values of IL-6 release in the olive oil diet. The study also showed that epinephrine regulation of IL-6 release was related to the diet.
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References
Spiegelman BM, Flier JS . Adipogenesis and obesity: rounding out the big picture. Cell 1996; 87: 377–389.
Sopasakis VR, Sandqvist M, Gustafson B, Hammarstedt A, Schmelz M, Yang X et al. High local concentrations and effects on differentiation implicate interleukin-6 as a paracrine regulator. Obes Res 2004; 12: 454–460.
Kishimoto T, Hirano T . Molecular regulation of B lymphocyte response. Annu Rev Immunol 1988; 6: 485–512.
Mitani H, Katayama N, Araki H, Ohishi K, Kobayashi K, Suzuki H et al. Activity of interleukin 6 in the differentiation of monocytes to macrophages and dendritic cells. Br J Haematol 2000; 109: 288–295.
Pedersen BK, Steensberg A, Fischer C, Keller C, Keller P, Plomgaard P et al. Searching for the exercise factor: is IL-6 a candidate? J Muscle Res Cell Motil 2003; 24: 113–119.
Sabio G, Das M, Mora A, Zhang Z, Jun JY, Ko HJ et al. A stress signaling pathway in adipose tissue regulates hepatic insulin resistance. Science 2008; 322: 1539–1543.
Eder K, Baffy N, Falus A, Fulop AK . The major inflammatory mediator interleukin-6 and obesity. Inflamm Res 2009; 58: 727–736.
Black PH . The inflammatory consequences of psychologic stress: relationship to insulin resistance, obesity, atherosclerosis and diabetes mellitus, type II. Med Hypotheses 2006; 67: 879–891.
Vicennati V, Vottero A, Friedman C, Papanicolaou DA . Hormonal regulation of interleukin-6 production in human adipocytes. Int J Obes Relat Metab Disord 2002; 26: 905–911.
Goossens GH, Jocken JW, van Baak MA, Jansen EH, Saris WH, Blaak EE . Short-term beta-adrenergic regulation of leptin, adiponectin and interleukin-6 secretion in vivo in lean and obese subjects. Diabetes Obes Metab 2008; 10: 1029–1038.
Budge H, Sebert S, Sharkey D, Symonds ME . Session on ‘Obesity’. Adipose tissue development, nutrition in early life and its impact on later obesity. Proc Nutr Soc 2009; 68: 321–326.
Soriguer F, Moreno F, Rojo-Martinez G, Cardona F, Tinahones F, Gomez-Zumaquero JM et al. Redistribution of abdominal fat after a period of food restriction in rats is related to the type of dietary fat. Br J Nutr 2003; 89: 115–122.
Juhasz A, Katona E, Csongradi E, Paragh G . [The regulation of body mass and its relation to the development of obesity]. Orv Hetil 2007; 148: 1827–1836.
Jimenez-Gomez Y, Lopez-Miranda J, Blanco-Colio LM, Marin C, Perez-Martinez P, Ruano J et al. Olive oil and walnut breakfasts reduce the postprandial inflammatory response in mononuclear cells compared with a butter breakfast in healthy men. Atherosclerosis 2009; 204: e70–e76.
Hennig B, Meerarani P, Ramadass P, Watkins BA, Toborek M . Fatty acid-mediated activation of vascular endothelial cells. Metabolism 2000; 49: 1006–1013.
Reeves PG, Nielsen FH, Fahey Jr GC . AIN-93 purified diets for laboratory rodents: final report of the American Institute of Nutrition ad hoc writing committee on the reformulation of the AIN-76A rodent diet. J Nutr 1993; 123: 1939–1951.
Hamilton S, Hamilton RJ, Sewell PA . Extraction of lipids and derivative formation. In: Hamilton RJ, Hamilton S (eds). Lipid Analysis. A Practical Approach. Oxford University Press: Oxford, 1992.
Soriguer F, Rojo-Martinez G, Dobarganes MC, Garcia Almeida JM, Esteva I, Beltran M et al. Hypertension is related to the degradation of dietary frying oils. Am J Clin Nutr 2003; 78: 1092–1097.
Rodbell M . Metabolism of isolated fat cells. VI. The effects of insulin, lipolytic hormones, and theophylline on glucose transport and metabolism in ‘ghosts’. J Biol Chem 1967; 242: 5751–5756.
Goldrick RB . Morphological changes in the adipocyte during fat deposition and mobilization. Am J Physiol 1967; 212: 777–782.
DiGirolamo M, Fine JB, Tagra K, Rossmanith R . Qualitative regional differences in adipose tissue growth and cellularity in male Wistar rats fed ad libitum. Am J Physiol 1998; 274: R1460–R1467.
Spranger J, Kroke A, Mohlig M, Hoffmann K, Bergmann MM, Ristow M et al. Inflammatory cytokines and the risk to develop type 2 diabetes: results of the prospective population-based European Prospective Investigation into Cancer and Nutrition (EPIC)-Potsdam Study. Diabetes 2003; 52: 812–817.
Flachs P, Mohamed-Ali V, Horakova O, Rossmeisl M, Hosseinzadeh-Attar MJ, Hensler M et al. Polyunsaturated fatty acids of marine origin induce adiponectin in mice fed a high-fat diet. Diabetologia 2006; 49: 394–397.
Hoene M, Weigert C . The role of interleukin-6 in insulin resistance, body fat distribution and energy balance. Obes Rev 2008; 9: 20–29.
Garcia-Escobar E, Soriguer F, Garcia-Serrano S, Gomez-Zumaquero JM, Morcillo S, Haro J et al. Dietary oleic acid and adipocyte lipolytic activity in culture. J Nutr Biochem 2008; 19: 727–731.
Pinkney JH, Coppack SW, Mohamed-Ali V . Effect of isoprenaline on plasma leptin and lipolysis in humans. Clin Endocrinol (Oxf) 1998; 48: 407–411.
Acknowledgements
We are grateful to Ian Johnstone for help with the English language version of the paper. This study was undertaken with financial support from the Fondo de Investigación Sanitaria of the Instituto de Salud Carlos III (PI021480 and the Metabolism and Nutrition Network RCMYN C03-08) and Junta de Andalucía (02/03, 125/02, 115/02).
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García-Escobar, E., Rodríguez-Pacheco, F., García-Serrano, S. et al. Nutritional regulation of interleukin-6 release from adipocytes. Int J Obes 34, 1328–1332 (2010). https://doi.org/10.1038/ijo.2010.70
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DOI: https://doi.org/10.1038/ijo.2010.70
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