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Body adiposity and bone parameters of male rats from mothers fed diet containing flaxseed flour during lactation

Published online by Cambridge University Press:  07 December 2015

C. A. S. da Costa*
Affiliation:
Laboratory of Experimental Nutrition, Department of Nutrition and Dietetics, Fluminense Federal University, Niterói, Brazil
P. C. A. da Silva
Affiliation:
Laboratory of Experimental Nutrition, Department of Nutrition and Dietetics, Fluminense Federal University, Niterói, Brazil
D. C. Ribeiro
Affiliation:
Laboratory of Experimental Nutrition, Department of Nutrition and Dietetics, Fluminense Federal University, Niterói, Brazil
A. D. D. Pereira
Affiliation:
Laboratory of Experimental Nutrition, Department of Nutrition and Dietetics, Fluminense Federal University, Niterói, Brazil
A. d. S. d. Santos
Affiliation:
Physiological Sciences, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro, Rio de Janeiro, Brazil
L. d. A. Maia
Affiliation:
Physiological Sciences, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro, Rio de Janeiro, Brazil
L. D. G. Ruffoni
Affiliation:
Laboratory of Exercise Physiology, Federal University of São Carlos, São Paulo, Brazil
F. C. de Santana
Affiliation:
Laboratory of Lipids, Department of Food Science and Experimental Nutrition, Faculty of Pharmaceutical Sciences, University of São Paulo, São Paulo, Brazil
M. D. C. de Abreu
Affiliation:
Laboratory of Experimental Nutrition, Department of Nutrition and Dietetics, Fluminense Federal University, Niterói, Brazil
B. F. d. C. Boueri
Affiliation:
Laboratory of Experimental Nutrition, Department of Nutrition and Dietetics, Fluminense Federal University, Niterói, Brazil
C. R. Pessanha
Affiliation:
Laboratory of Experimental Nutrition, Department of Nutrition and Dietetics, Fluminense Federal University, Niterói, Brazil
K. O. Nonaka
Affiliation:
Laboratory of Exercise Physiology, Federal University of São Carlos, São Paulo, Brazil
J. Mancini-Filho
Affiliation:
Laboratory of Lipids, Department of Food Science and Experimental Nutrition, Faculty of Pharmaceutical Sciences, University of São Paulo, São Paulo, Brazil
C. C. A. do Nascimento-Saba
Affiliation:
Physiological Sciences, Institute of Biology Roberto Alcantara Gomes, State University of Rio de Janeiro, Rio de Janeiro, Brazil
G. T. Boaventura
Affiliation:
Laboratory of Experimental Nutrition, Department of Nutrition and Dietetics, Fluminense Federal University, Niterói, Brazil
*
*Address for correspondence: C. A. S. da Costa, Experimental Nutrition Laboratory, College of Nutrition, Federal Fluminense University, Rua Mário Santos Braga, 30, Niterói, RJ 24015-110, Brazil. (Email nutcarlos@hotmail.com)

Abstract

Obesity and osteoporosis may have their origins in early postnatal life. This study was designed to evaluate whether flaxseed flour use during lactation period bears effect on body adiposity and skeletal structure of male rat pups at weaning. At birth, male Wistar rats were randomly assigned to control and experimental (FF) groups, whose dams were treated with control or flaxseed flour diet, respectively, during lactation. At 21 days of age, pups were weaned to assess body mass, length and composition by dual-energy X-ray absorptiometry. The animals were then sacrificed to carry out analysis of serum profile, intra-abdominal adipocyte morphology and femur characteristics. Differences were considered significant when P<0.05. The FF group displayed the following characteristics (P<0.05): higher body mass, length, bone mineral content, bone area and concentrations of osteoprotegerin, osteocalcin and high-density lipoprotein cholesterol; higher levels of stearic, α-linolenic, eicosapentaenoic and docosapentaenoic acids and lower levels of arachidonic acid and cholesterol; smaller adipocyte area; and higher mass, epiphysis distance, diaphysis width, maximal load, break load, resilience and stiffness of femur. Flaxseed flour intake during lactation period promoted adipocyte hypertrophy down-regulation and contributed to pup bone quality at weaning.

Type
Original Article
Copyright
© Cambridge University Press and the International Society for Developmental Origins of Health and Disease 2015 

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References

1. Hochberg, Z. Evo Devo of Child Growth: Treatise on Child Growth and Human Evolution. 2012. Miley: New York, NY.Google Scholar
2. Golding, J, Rogers, IS, Emmett, PM. Association between breast feeding, child development and behavior. Early Hum Dev. 1997; 29, 175184.CrossRefGoogle Scholar
3. Cooper, C, Westlake, S, Harvey, N, et al. Review: developmental origins of osteoporotic fracture. Osteoporos Int. 2006; 17, 337347.CrossRefGoogle ScholarPubMed
4. Green, KH, Wong, SCF, Weiler, HA. The effect of dietary n-3 long-chain polyunsaturated fatty acids on femur mineral density and biomarkers of bone metabolism in healthy diabetic and dietary-restricted growing rats. Prostaglandins Leukot Essent Fatty Acids. 2004; 71, 121130.CrossRefGoogle ScholarPubMed
5. Costa, CAS, Carlos, AS, Santos, AS, et al. Abdominal adiposity, insulin and bone quality in young male rats fed a high-fat diet containing soybean or canola oil. Clinics (São Paulo). 2011; 66, 18111816.CrossRefGoogle ScholarPubMed
6. Costa, CAS, Carlos, AS, Gonzalez, GP, et al. Diet containing low n-6/n-3 polyunsaturated fatty acids ratio, provided by canola oil, alters body composition and bone quality in young rats. Eur J Nutr. 2012; 51, 191198.CrossRefGoogle ScholarPubMed
7. Kruger, MC, Coetzee, M, Haag, M, Weiler, H. Long-chain polyunsaturated fatty acids: selected mechanisms of action on bone. Prog Lipid Res. 2010; 49, 438449.CrossRefGoogle ScholarPubMed
8. Ruxton, CHS, Reed, SC, Simpson, MJ, Millington, KJ. The health benefits of omega-3 polyunsaturated fatty acids: a review of the evidence. J Hum Nutr Diet. 2004; 17, 449459.CrossRefGoogle ScholarPubMed
9. Leite, CDFC, Vicente, GC, Suzuki, A, et al. Effects of flaxseed on rat milk creamatocrit and its contribution to offspring body growth. J Pediatr. 2012; 88, 7478.CrossRefGoogle ScholarPubMed
10. Pacheco, JT, Delaprame, JB, Boaventura, GT. Impact of dietary flaxseed (Linum usitatissimum) supplementation on biochemical profile in healthy rats. Nutr Hosp. 2011; 26, 798802.Google Scholar
11. Goyal, A, Sharma, V, Upadhyay, N, Gill, S, Sihag, M. Flax and flaxseed oil: an ancient medicine & modern functional food. J Food Sci Technol. 2014; 51, 16331653.CrossRefGoogle ScholarPubMed
12. Ribeiro, ICA, da Costa, CAS, Pereira, VA, Boaventura, GT, Chagas, MA. Effects of flaxseed flour on the lipid profile of rats submitted to prolonged androgen stimuli. Nutr Hosp. 2014; 30, 825830.Google ScholarPubMed
13. Daleprane, JB, Batista, A, Pacheco, JT, et al. Dietary flaxseed supplementation improves endothelial function in the mesenteric arterial bed. Food Res Int. 2010; 43, 20522056.CrossRefGoogle Scholar
14. Leite, CDFC, Almeida, KCL, Gúzman-Silva, MA, Meneses, JA, Boaventura, GT. Flaxseed and its contribution to body growth and brain of Wistar rats during childhood and adolescence. Nutr Hosp. 2006; 26, 415420.Google Scholar
15. Cardozo, LFMF, Soares, LL, Brant, LHC, et al. Hematological and immunological are altered by chronic intake of flaxseed in Wistar rats. Nutr Hosp. 2011; 26, 10911096.Google Scholar
16. Fishbeck, KL, Rasmussen, KM. Effect of repeated cycles on maternal nutritional status, lactational performance and litter growth in ad libitum-fed and chronically food-restricted rat. J Nutr. 1987; 117, 19671975.CrossRefGoogle Scholar
17. Reeves, PG. Components of the AIN-93 diets as improvements in the AIN-76A diet. J Nutr. 1997; 127, 838841.CrossRefGoogle ScholarPubMed
18. Lukaski, HC, Hall, CB, Marchello, MJ, Siders, WA. Validation of dual X-ray absorptiometry for body-composition assessment of rats exposed to dietary stressors. Nutrition. 2001; 17, 607613.CrossRefGoogle ScholarPubMed
19. Ribeiro, DC, da Silva, PCA, Pereira, AD, et al. Assessments of body composition and bone parameters of lactating rats treated with diet containing flaxseed meal (Linum usitatissimum) during post-weaning period. Nutr Hosp. 2014; 30, 366371.Google Scholar
20. AOAC. Official Methods of Analysis. 2002. AOAC International: Gaithersburg.Google Scholar
21. AOCS. Determination of Cis-, Trans-, Saturated, Monounsaturated, and Polyunsaturated Fatty Acids in Vegetable or Non-Ruminant Animal Oils and Fats by Capillary GLC. Official Method Ce 1h-05. 2005. AOCS Press: Champaign, IL.Google Scholar
22. Trebacz, H, Zduneck, A. Three-point bending and acoustic emission study of adult rat femora after immobilization and free remobilization. J Biomech. 2006; 39, 237245.CrossRefGoogle ScholarPubMed
23. Tinoco, SMB, Sichieri, R, Setta, CL, Moura, AS, Carmo, MGT. n-3 Polyunsaturated fatty acids in milk is associate to weight gain and growth in premature infants. Lipids Health Dis. 2009; 8, 23.CrossRefGoogle ScholarPubMed
24. McCullough, RS, Edel, AL, Bassett, CMC, et al. The alpha linolenic acid content of flaxseed is associated with an induction of adipose leptin expression. Lipids. 2011; 46, 10431052.CrossRefGoogle ScholarPubMed
25. Gebauer, SK, Psota, TL, Harris, WS, Kris-Etherton, PM. n-3 Fatty acid dietary recommendations and food sources to achieve essentiality and cardiovascular benefits. Am J Clin Nutr. 2006; 83, 15261535.CrossRefGoogle ScholarPubMed
26. Massiera, F, Saint-Marc, P, Seydoux, J, et al. Arachidonic acid and prostacyclin signaling promote adipose tissue development: a human health concern? J Lipid Res. 2003; 44, 271279.CrossRefGoogle ScholarPubMed
27. Hsu, SC, Huang, CJ. Reduced fat mass in rats fed a high oleic acid-rich safflower oil diet is associated with changes in expression of hepatic PPARα and adipose SREBP-1c-regulated genes. J Nutr. 2006; 136, 17791785.CrossRefGoogle ScholarPubMed
28. Pellizzon, MA, Billheimer, JT, Bloedon, LT, Szapary, PO, Rader, DJ. Flaxseed reduces plasma cholesterol levels in hypercholesterolemic mouse models. J Am Coll Nutr. 2007; 26, 6675.CrossRefGoogle ScholarPubMed
29. Dietschy, JM, Woollett, LA, Spady, DK. The interaction of dietary cholesterol and specific fatty acids in the regulation of LDL receptor activity and plasma LDL cholesterol concentrations. Ann N Y Acad Sci. 1993; 676, 1126.CrossRefGoogle ScholarPubMed
30. Pearson, TA. Metabolic consequences of stearic acid relative to long-chain fatty acids. Paper presented to conference on metabolic consequences of stearic acid relative to other long-chain fatty acids. Nutr Res. 1993; 5, 56.Google Scholar
31. Go, J, Song, Y, Park, JH, Park, JY, Choi, YH. Association between serum cholesterol level and bone mineral density at lumbar spine and femur neck in postmenopausal Korean women. Korean J Fam Med. 2012; 33, 166173.CrossRefGoogle ScholarPubMed
32. You, L, Sheng, Z, Tang, CL, et al. High cholesterol diet increases osteoporosis risk via inhibiting bone formation in rats. Acta Pharmacol Sin. 2011; 32, 14981504.CrossRefGoogle ScholarPubMed
33. Jeong, I, Cho, SW, Kim, SW, et al. Lipid profiles and bone mineral density in pre- and postmenopausal women in Korea. Calcif Tissue Int. 2010; 87, 507512.CrossRefGoogle ScholarPubMed
34. Corwin, RL. Effects of dietary fats on bone health in advanced age. Prostaglandins Leukot Essent Fatty Acids. 2003; 68, 379386.CrossRefGoogle Scholar
35. Tsujio, M, Mizorogi, T, Kitamura, I, et al. Bone mineral analysis through dual energy X-ray absorptiometry in laboratory animals. J Vet Med Sci. 2009; 71, 14931497.CrossRefGoogle ScholarPubMed
36. Ward, WE, Yuan, YV, Cheung, AM, Thompson, LU. Exposure to flaxseed and its purified lignan reduces bone strength in young but not older male rats. J Toxicol Environ Health. 2010; 11, 5365.Google Scholar