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A specific dose of grape seed-derived proanthocyanidins to inhibit body weight gain limits food intake and increases energy expenditure in rats

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Abstract

Purpose

Several studies have suggested that flavanols may have antiobesity effects; however, those effects clearly depend on the experimental conditions. In a previous study, we found that a single acute dose of grape seed proanthocyanidin extract (GSPE) has satiating effects. We therefore hypothesise that satiating doses of GSPE could be used to reduce body weight gain, and our present objective was to define the most effective dose.

Methods

We assayed two GSPE doses in aged male Wistar rats. First we performed a subchronic (8-day) treatment by intragastric administration, which was repeated after a washout period. We measured body weight, energy intake and faeces composition; we performed indirect calorimetry; and we analysed the mRNA expression of genes involved in lipid metabolism to determine the target tissue for the GSPE.

Results

We observed that 0.5 g GSPE/kg BW significantly reduced food intake and thus the amount of energy absorbed. This dosage also increased lipid oxidation in subcutaneous adipose tissue, thus causing a higher total energy expenditure. These combined effects caused a decrease in body weight. Conversely, 1 g GSPE/kg BW, which also reduced energy absorption after the first treatment, had a rebound effect on body weight gain which resulted in a lower response to the proanthocyanidin extract. That is, after the second treatment, the GSPE did not reduce the energy absorbed or modify energy expenditure and body weight.

Conclusion

GSPE at a dose of 0.5 g/kg can reduce body weight by limiting food intake and activating energy expenditure in subcutaneous adipose tissue.

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References

  1. Wang YC, McPherson K, Marsh T et al (2015) Health and economic burden of the projected obesity trends in the USA and the UK. Lancet 378:815–825. doi:10.1016/S0140-6736(11)60814-3

    Article  Google Scholar 

  2. Landete JM (2011) Updated knowledge about polyphenols: functions, bioavailability, metabolism, and health. Crit Rev Food Sci Nutr 52:936–948. doi:10.1080/10408398.2010.513779

    Article  Google Scholar 

  3. Salvadó MJ, Casanova E, Fernández-Iglesias A et al (2015) Roles of proanthocyanidin rich extracts in obesity. Food Funct 6:1053–1071. doi:10.1039/C4FO01035C

    Article  Google Scholar 

  4. Bladé C, Arola L, Salvadó M-J (2010) Hypolipidemic effects of proanthocyanidins and their underlying biochemical and molecular mechanisms. Mol Nutr Food Res 54:37–59

    Article  Google Scholar 

  5. Lee YA, Cho EJ, Tanaka T, Yokozawa T (2007) Inhibitory activities of proanthocyanidins from persimmon against oxidative stress and digestive enzymes related to diabetes. J Nutr Sci Vitaminol 53:287–292

    Article  CAS  Google Scholar 

  6. Mcdougall GJ, Stewart D (2005) The inhibitory effects of berry polyphenols on digestive enzymes. BioFactors 23:189–195. doi:10.1002/biof.5520230403

    Article  CAS  Google Scholar 

  7. Gonzalez-Abuin N, González-Abuín N, Martínez-Micaelo N et al (2014) Grape-seed procyanidins prevent the cafeteria-diet-induced decrease of glucagon-like peptide-1 production. J Agric Food Chem 62:1066–1072. doi:10.1021/jf405239p

    Article  CAS  Google Scholar 

  8. González-Abuín N, Martínez-Micaelo N, Margalef M et al (2014) A grape seed extract increases active glucagon-like peptide-1 levels after an oral glucose load in rats. Food Funct 5:2357–2364. doi:10.1039/c4fo00447g

    Article  Google Scholar 

  9. Serrano J, Casanova-Martí À, Gil-Cardoso K, Blay MT, Terra X, Pinent P, Ardévol A (2016) Acutely administrated grape-seed proanthocyanidin extract acts as a satiating agent. Food Funct 7:483–490. doi:10.1039/c5fo00892a

    Article  CAS  Google Scholar 

  10. Quiñones M, Guerrero L, Suarez M et al (2013) Low-molecular procyanidin rich grape seed extract exerts antihypertensive effect in males spontaneously hypertensive rats. Food Res Int 51:587–595

    Article  Google Scholar 

  11. Soares S, Brandão E, Mateus N, De Freitas V (2015) Sensorial properties of red wine polyphenols: astringency and bitterness. Crit Rev Food Sci Nutr. doi:10.1080/10408398.2014.946468

    Google Scholar 

  12. Salvadó MJ, Casanova E, Fernández-iglesias A et al (2015) Roles of proanthocyanidin rich extracts in obesity. Food Funct 6:1053–1071. doi:10.1039/c4fo01035c

    Article  Google Scholar 

  13. Tebib K, Besançon P, Rouanet JM (1996) Effects of dietary grape seed tannins on rat cecal fermentation and colonic bacterial enzymes. Nutr Res 16:105–110. doi:10.1016/0271-5317(95)02064-0

    Article  CAS  Google Scholar 

  14. Goncalves R, Mateus N, De Freitas V (2010) Study of the interaction of pancreatic lipase with procyanidins by optical and enzymatic methods. J Agric Food Chem 58:11901–11906. doi:10.1021/jf103026x

    Article  CAS  Google Scholar 

  15. Yilmazer-Musa M, Griffith AM, Michels AJ et al (2012) Grape seed and tea extracts and catechin 3-gallates are potent inhibitors of α-amylase and α-glucosidase activity. J Agric Food Chem 60:8924–8929. doi:10.1021/jf301147n

    Article  CAS  Google Scholar 

  16. Gonçalves R, Mateus N, de Freitas V (2010) Biological relevance of the interaction between procyanidins and trypsin: a multitechnique approach. J Agric Food Chem 58:11924–11931. doi:10.1021/jf1023356

    Article  Google Scholar 

  17. Tebib K, Rouanet JM, Besançon P (1994) Effect of grape seed tannins on the activity of some rat intestinal enzyme activities. Enzyme Protein 48:51–60

    CAS  Google Scholar 

  18. Pinent M, Blay M, Serrano J, Ardévol A (2015) Effects of flavanols on the enteroendocrine system: repercussions on food intake. Crit Rev Food Sci Nutr. doi:10.1080/10408398.2013.871221

    Google Scholar 

  19. Panickar KS (2013) Effects of dietary polyphenols on neuroregulatory factors and pathways that mediate food intake and energy regulation in obesity. Mol Nutr Food Res 57:34–47. doi:10.1002/mnfr.201200431

    Article  CAS  Google Scholar 

  20. Bao L, Cai X, Dai X et al (2014) Grape seed proanthocyanidin extracts ameliorate podocyte injury by activating peroxisome proliferator-activated receptor-γ coactivator 1α in low-dose streptozotocin-and high-carbohydrate/high-fat diet-induced diabetic rats. Food Funct 5:1872–1880. doi:10.1039/c4fo00340c

    Article  CAS  Google Scholar 

  21. Assaad H, Yao K, Tekwe CD et al (2014) Analysis of energy expenditure in diet-induced obese rats. Front Biosci (Landmark Ed) 19:967–985

    Article  Google Scholar 

  22. Most J, Goossens GH, Jocken JWE, Blaak EE (2014) Short-term supplementation with a specific combination of dietary polyphenols increases energy expenditure and alters substrate metabolism in overweight subjects. Int J Obes (Lond) 38:698–706. doi:10.1038/ijo.2013.231

    Article  CAS  Google Scholar 

  23. Rondanelli M, Opizzi A, Perna S et al (2013) Acute effect on satiety, resting energy expenditure, respiratory quotient, glucagon-like peptide-1, free fatty acids, and glycerol following consumption of a combination of bioactive food ingredients in overweight subjects. J Am Coll Nutr 32:41–49. doi:10.1080/07315724.2013.767667

    Article  CAS  Google Scholar 

  24. Hursel R, Viechtbauer W, Dulloo AG et al (2011) The effects of catechin rich teas and caffeine on energy expenditure and fat oxidation: a meta-analysis. Obes Rev 12:e573–e581. doi:10.1111/j.1467-789X.2011.00862.x

    Article  CAS  Google Scholar 

  25. Da-Silva WS, Harney JW, Kim BW et al (2007) The small polyphenolic molecule kaempferol increases cellular energy expenditure and thyroid hormone activation. Diabetes 56:767–776. doi:10.2337/db06-1488

    Article  CAS  Google Scholar 

  26. Gruendel S, Garcia AL, Otto B et al (2006) Carob pulp preparation rich in insoluble dietary fiber and polyphenols enhances lipid oxidation and lowers postprandial acylated ghrelin in humans. J Nutr 136:1533–1538

    CAS  Google Scholar 

  27. Bérubé-Parent S, Pelletier C, Doré J, Tremblay A (2005) Effects of encapsulated green tea and Guarana extracts containing a mixture of epigallocatechin-3-gallate and caffeine on 24 h energy expenditure and fat oxidation in men. Br J Nutr 94:432–436

    Article  Google Scholar 

  28. Klaus S, Pültz S, Thöne-Reineke C, Wolfram S (2005) Epigallocatechin gallate attenuates diet-induced obesity in mice by decreasing energy absorption and increasing fat oxidation. Int J Obes (Lond) 29:615–623. doi:10.1038/sj.ijo.0802926

    Article  CAS  Google Scholar 

  29. Komatsu T, Nakamori M, Komatsu K et al (2003) Oolong tea increases energy metabolism in Japanese females. J Med Invest 50:170–175

    Google Scholar 

  30. Dulloo AG, Duret C, Rohrer D et al (1999) Efficacy of a green tea extract rich in catechin polyphenols and caffeine in increasing 24-h energy expenditure and fat oxidation in humans. Am J Clin Nutr 70:1040–1045

    CAS  Google Scholar 

  31. Casanova E, Baselga-Escudero L, Ribas-Latre A et al (2014) Chronic intake of proanthocyanidins and docosahexaenoic acid improves skeletal muscle oxidative capacity in diet-obese rats. J Nutr Biochem 25:1003–1010. doi:10.1016/j.jnutbio.2014.05.003

    Article  CAS  Google Scholar 

  32. Crescenti A, del Bas JM, Arola-Arnal A et al (2015) Grape seed procyanidins administered at physiological doses to rats during pregnancy and lactation promote lipid oxidation and up-regulate AMPK in the muscle of male offspring in adulthood. J Nutr Biochem. doi:10.1016/j.jnutbio.2015.03.003

    Google Scholar 

  33. Caimari A, del Bas JM, Crescenti A, Arola L (2012) Low doses of grape seed procyanidins reduce adiposity and improve the plasma lipid profile in hamsters. Int J Obes 37:576–583. doi:10.1038/ijo.2012.75

    Article  Google Scholar 

  34. Margalef M, Pons Z, Bravo FI et al (2015) Tissue distribution of rat flavanol metabolites at different doses. J Nutr Biochem. doi:10.1016/j.jnutbio.2015.04.006

    Google Scholar 

  35. Baiges I, Palmfeldt J, Blade C et al (2010) Lipogenesis is decreased by grape seed proanthocyanidins according to liver proteomics of rats fed a high fat diet. Mol Cell Proteom. doi:10.1074/mcp.M000055-MCP201

    Google Scholar 

  36. Wajchenberg BL (2000) Subcutaneous and visceral adipose tissue: their relation to the metabolic syndrome. Endocr Rev 21:697–738. doi:10.1210/edrv.21.6.0415

    Article  CAS  Google Scholar 

  37. Freedland ES (2004) Role of a critical visceral adipose tissue threshold (CVATT) in metabolic syndrome: implications for controlling dietary carbohydrates: a review. Nutr Metab (Lond) 1:12. doi:10.1186/1743-7075-1-12

    Article  Google Scholar 

  38. Ardévol A, Motilva MJ, Serra A et al (2013) Procyanidins target mesenteric adipose tissue in Wistar lean rats and subcutaneous adipose tissue in Zucker obese rat. Food Chem 141:160–166. doi:10.1016/j.foodchem.2013.02.104

    Article  Google Scholar 

Download references

Acknowledgments

We would like to express our thanks to Niurka Llopiz for her technical support. We also thank the Technological Center of Nutrition and Health for the use of their animal facilities. This work has been supported by a Grant (AGL2014-55347-R) from the Spanish government. Àngela Casanova received a grant for Ph.D. students from Universitat Rovira i Virgili. Joan Serrano received a pre-doctoral fellowship from the Government of Catalonia. Montserrat Pinent is a Serra Húnter fellow.

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Correspondence to Anna Ardévol.

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Joan Serrano and Àngela Casanova-Martí have contributed equally to this work.

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394_2016_1209_MOESM1_ESM.docx

Figure S1. Rebooting after treatment 1. Body weight in aged male Wistar rats was measured every 2 days after treatment 1. Circles indicate control (vehicle-administered) animals; square indicates 0.5 g GSPE/kg BW dose; and triangles indicate 1 g GSPE/kg BW dose. Day 26 stopped the statistical (p < 0.05) differences between dose 1 and control group. Day 30 stopped the statistical (p < 0.05) differences between dose 0.5 and control group. (DOCX 19 kb)

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Serrano, J., Casanova-Martí, À., Gual, A. et al. A specific dose of grape seed-derived proanthocyanidins to inhibit body weight gain limits food intake and increases energy expenditure in rats. Eur J Nutr 56, 1629–1636 (2017). https://doi.org/10.1007/s00394-016-1209-x

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