Hypocaloric diet in perinatal life followed by obesity exacerbates metabolic disorders in the offspring of wistar rats

Autores/as

DOI:

https://doi.org/10.21527/2176-7114.2024.48.13981

Palabras clave:

Adaptive plasticity, high-fat diet, obesity, rats

Resumen

The effects of an obesogenic post-weaning diet on the growth and metabolic parameters of adult offspring submitted to a hypocaloric diet in perinatal life were evaluated. Male Wistar rats were divided into two groups according to maternal diet during pregnancy and lactation: Control (C, received normocaloric diet) and hypocaloric diet during pregnancy and lactation (H, received hypocaloric diet). At weaning, half the number of animals in each group was divided into two more groups according to the post-weaning diet: control (CC, n=12), control and subject to the obesogenic diet (CO n=11), hypocaloric diet and control (HC, n=14) and hypocaloric and obesogenic diet (HO, n=9). Maternal body weight, food intake, and energy intake were recorded daily. In the offspring, birth weight, growth rate, and physical characteristics were evaluated. At 120 days, relative food consumption, glucose tolerance test (GTT), biochemical profile, and organ weight were analyzed. Mothers on a low-calorie diet showed no difference in body weight during pregnancy or lactation even with lower energy intake. In offspring, litters from mothers fed a low-calorie diet showed a deficit in physical characteristics (growth restriction and low weight). The effect of an obesogenic diet on visceral fat weight, GTT, and hypercholesterolemia was most pronounced in animals subjected to a perinatal hypocaloric diet followed by a lifelong obesogenic diet. Conclusion: Our observations expand the evidence that social environments with food scarcity and/or obesogenic environments determine greater susceptibility to obesity.

Citas

Velazquez MA, Fleming TP, Watkins AJ. Periconceptional environment and the developmental origins of disease. Journal of Endocrinology. 2019 Jul;242(1):T33–49.

Sreevidya Sreekantha, Wang Y, Sakurai R, Liu J, Rehan VK. Maternal food restriction‐induced intrauterine growth restriction in a rat model leads to sex‐specific adipogenic programming. The FASEB Journal [Internet]. 2020 Oct 13 [cited 2023 Nov 19];34(12):16073–85.

Wen Y, Cheng S, Lu J, He X, Jiao Z, Xu D, et al. Dysfunction of the hypothalamic‑pituitary‑adrenal axis in male rat offspring with prenatal food restriction: Fetal programming of hypothalamic hyperexcitability and poor hippocampal feedback. Molecular Medicine Reports. 2021 Nov 18;25(1).

Fleming TP, Sun C, Oleg Denisenko, Caetano L, Anan Aljahdali, Gould JM, et al. Environmental Exposures around Conception: Developmental Pathways Leading to Lifetime Disease Risk. 2021 Sep 6;18(17):9380–0.

Gantenbein KV, Kanaka-Gantenbein C. Highlighting the trajectory from intrauterine growth restriction to future obesity. Frontiers in Endocrinology. 2022 Nov 11;13.

Hanson M, Godfrey KM, Lillycrop KA, Burdge GC, Gluckman PD. Developmental plasticity and developmental origins of non-communicable disease: Theoretical considerations and epigenetic mechanisms. Prog Biophys Mol Biol [Internet]. 2011;106(1):272–80. Available from: http://dx.doi.org/10.1016/j.pbiomolbio.2010.12.008

Ajuogu PK, Wolden M, McFarlane JR, Hart RA, Carlson DJ, Van der Touw T, et al. Effect of low- and high-protein maternal diets during gestation on reproductive outcomes in the rat: a systematic review and meta-analysis. Journal of Animal Science. 2019 Dec 19;98(1).

Kim J, Choi A, Kwon YH. Maternal Protein Restriction Altered Insulin Resistance and Inflammation-Associated Gene Expression in Adipose Tissue of Young Adult Mouse Offspring in Response to a High-Fat Diet. Nutrients. 2020 Apr 16;12(4):1103.

Devarajan A, Rajasekaran NS, Valburg C, Ganapathy E, Bindra S, Freije WA. Maternal perinatal calorie restriction temporally regulates the hepatic autophagy and redox status in male rat. Free Radic Biol Med. 2019;130:592–600.

Do Nascimento E, De Santana Muniz G, Das Graças De Santana Muniz M, De Souza Alexandre L, Da Rocha LS, Leandro CG, et al. Unlimited access to low-energy diet causes acute malnutrition in dams and alters biometric and biochemical parameters in offspring. J Dev Orig Health Dis. 2014;5(1):45–55.

Monte C. Malnutrition: a secular challenge to child nutrition. J Pediatr (Rio J). 2000;76(8):285–97.

Millward DJ. Protein requirements of infants. Am J Clin Nutr. 1989;50(2):406–7.

Krechowec SO, Vickers M, Gertler A, Breier BH. Prenatal influences on leptin sensitivity and susceptibility to diet-induced obesity. J Endocrinol. 2006;189(2):355–63.

Thompson NM, Norman AM, Donkin SS, Shankar RR, Vickers MH, Miles JL, et al. Prenatal and postnatal pathways to obesity: Different underlying mechanisms, different metabolic outcomes. Endocrinology. 2007;148(5):2345–54.

Vickers MH, Breier BH, McCarthy D, Gluckman PD. Sedentary behavior during postnatal life is determined by the prenatal environment and exacerbated by postnatal hypercaloric nutrition. Am J Physiol - Regul Integr Comp Physiol. 2003;285(1 54-1):271–3.

MacKay H, Khazall R, Patterson ZR, Wellman M, Abizaid A. Rats perinatally exposed to food restriction and high-fat diet show differences in adipose tissue gene expression under chronic caloric restriction. Adipocyte. 2013;2(4):237–45.

Lopes De Souza S, Orozco-Solis R, Grit I, Manhães De Castro R, Bolaños-Jiménez F. Perinatal protein restriction reduces the inhibitory action of serotonin on food intake. Eur J Neurosci. 2008;27(6):1400–8.

Le Floch JP, Escuyer P, Baudin E, Baudon D, Perlemuter L. Blood glucose area under the curve. Methodological aspects. Diabetes Care. 1990;13(2):172–5.

William T. Friedewald, Levy RI, Fredrickson DS. Estimation of the Concentration of Low-Density Lipoprotein Cholesterolin Plasma,Without Useof the Preparative Ultracentrifuge. J Chem Inf Model. 1972;18(6):1689–99.

Bateson P, Gluckman P, Hanson M. The biology of developmental plasticity and the Predictive Adaptive Response hypothesis. J Physiol. 2014;592(11):2357–68.

Nascimento E do, Muniz G de S, Silva AAM da, Santana R de A, Vasconcelos DAA de, Cavalcante TCF. Western-style diet changes murinometric and metabolic parameters of rat offspring in time-specific windows. Brazilian J Dev. 2020;6(7):48355–72.

Nascimento E, Guzman-Quevedo O, Delacourt N, da Silva Aragão R, Perez-Garcia G, de Souza SL, et al. Long-Lasting Effect of Perinatal Exposure to L-tryptophan on Circadian Clock of Primary Cell Lines Established from Male Offspring Born from Mothers Fed on Dietary Protein Restriction. PLoS One. 2013;8(2).

Roberts SB, Heyman MB. Dietary composition and obesity: Do we need to look beyond dietary fat? J Nutr. 2000;130(2 SUPPL.):272–5.

Nakashima Y, Sato A. PUPS of dams fed low-fat diet during pregnancy and lactation showed strong preference for high-fat diet to achieve optimal growth. J Nutr Sci Vitaminol (Tokyo). 2011;57(5):355–63.

Magnuson AM, Regan DP, Booth AD, Fouts JK, Solt CM, Hill JL, et al. High-fat diet induced central adiposity (visceral fat) is associated with increased fibrosis and decreased immune cellularity of the mesenteric lymph node in mice. Eur J Nutr [Internet]. 2020;59(4):1641–54. Available from: https://doi.org/10.1007/s00394-019-02019-z

Butruille L, Marousez L, Pourpe C, Oger F, Lecoutre S, Catheline D, et al. Maternal high-fat diet during suckling programs visceral adiposity and epigenetic regulation of adipose tissue stearoyl-CoA desaturase-1 in offspring. Int J Obes [Internet]. 2019;43(12):2381–93. Available from: http://dx.doi.org/10.1038/s41366-018-0310-z

Viraragavan A, Willmer T, Patel O, Basson A, Johnson R, Pheiffer C. Cafeteria diet induces global and Slc27a3-specific hypomethylation in male Wistar rats. Adipocyte [Internet]. 2021;10(1):108–18. Available from: https://doi.org/10.1080/21623945.2021.1886697

Ozanne SE, Jensen CB, Tingey KJ, Storgaard H, Madsbad S, Vaag AA. Low birthweight is associated with specific changes in muscle insulin-signalling protein expression. Diabetologia. 2005;48(3):547–52.

Huang BW, Chiang MT, Yao HT, Chiang W. The effect of high-fat and high-fructose diets on glucose tolerance and plasma lipid and leptin levels in rats. Diabetes, Obes Metab. 2004;6(2):120–6.

Schaalan M, El-Abhar HS, Barakat M, El-Denshary ES. Westernized-like-diet-fed rats: effect on glucose homeostasis, lipid profile, and adipocyte hormones and their modulation by rosiglitazone and glimepiride. J Diabetes Complications [Internet]. 2009;23(3):199–208. Available from: http://dx.doi.org/10.1016/j.jdiacomp.2008.02.003

Alejandro EU, Jo S, Akhaphong B, Llacer PR, Gianchandani M, Gregg B, et al. Maternal low-protein diet on the last week of pregnancy contributes to insulin resistance 2 and β-cell dysfunction in the mouse offspring. 2020.

Vidal-Santos R, Macedo FN, Santana MNS, De Melo VU, De Brito Alves JL, Santos MRV, et al. Western diet in the perinatal period promotes dysautonomia in the offspring of adult rats. J Dev Orig Health Dis. 2017;8(2):216–25.

Zinkhan EK, Yu B, Callaway CW, McKnight RA. Intrauterine growth restriction combined with a maternal high-fat diet increased adiposity and serum corticosterone levels in adult rat offspring. J Dev Orig Health Dis. 2018;9(3):315–28.

Descargas

Publicado

2024-06-24

Cómo citar

Araújo, L. L., do Nascimento, E., Franco, E. de S., Souto, V. F., Melo, M. C. A. de L., Muniz, G. de S., & Leandro, C. V. G. (2024). Hypocaloric diet in perinatal life followed by obesity exacerbates metabolic disorders in the offspring of wistar rats. Revista Contexto &Amp; Saúde, 24(48), e13981. https://doi.org/10.21527/2176-7114.2024.48.13981

Número

Sección

Artigo Original