Hostname: page-component-78c5997874-dh8gc Total loading time: 0 Render date: 2024-11-19T05:34:08.688Z Has data issue: false hasContentIssue false

Prenatal exposure to a maternal low-protein diet programmes a preference for high-fat foods in the young adult rat

Published online by Cambridge University Press:  09 March 2007

Leanne Bellinger
Affiliation:
Centre for Reproduction and Early Life, School of Biosciences, University of Nottingham, Sutton Bonington, Loughborough LE12 5RD, UK
Christina Lilley
Affiliation:
Centre for Reproduction and Early Life, School of Biosciences, University of Nottingham, Sutton Bonington, Loughborough LE12 5RD, UK
Simon C. Langley-Evans*
Affiliation:
Centre for Reproduction and Early Life, School of Biosciences, University of Nottingham, Sutton Bonington, Loughborough LE12 5RD, UK
*
*Corresponding author: fax +44 115 951 6122, Email [email protected]
Rights & Permissions [Opens in a new window]

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.

Nutrient restriction in pregnancy has been shown to programme adult obesity. Modulation of feeding behaviour may provide a mechanism through which obesity may be programmed. Pregnant Wistar rats were fed either a control diet or a low-protein (LP) diet throughout gestation. Their offspring were allocated to a self-selected-diet protocol to assess appetite and food preferences at 12 and at 30 weeks of age. Self-selection of high-fat, high-protein or high-carbohydrate foods by 12-week-old rats indicated that the prenatal environment influenced feeding behaviour. Both male and female offspring of LP-fed mothers consumed significantly more of the high-fat (P>0·001) and significantly less (P>0·02) of the high-carbohydrate food than the control animals. Female, but not male, offspring of LP-fed rats failed to adjust food intake to maintain a constant energy intake and had higher fat (P>0·005) and energy intakes (P>0·05) than control female rats. At 30 weeks of age there were no differences in the pattern of food selection between the two groups of animals. Male offspring of LP-fed rats had significantly more gonadal fat than control animals (P>0·05), but analysis of total body fat content indicated that there was no significant difference in overall adiposity. The present study suggests that in young adults at least, early life exposure to undernutrition determines a preference for fatty foods. Maternal nutrition may thus promote changes in systems that are involved in control of appetite or the perception of palatability.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2004

References

Anguita, RM, Sigulem, DM & Sawaya, ALIntrauterine food restriction is associated with obesity in young rats. J Nutr (1993) 123, 14211428Google ScholarPubMed
Barker, DJPThe developmental origins of adult disease. Eur J Epidemiol (2003) 18, 733736CrossRefGoogle ScholarPubMed
Bergel, E & Belizan, JMA deficient maternal calcium intake during pregnancy increases blood pressure of the offspring in adult rats. Br J Obstet Gynaecol (2002) 109, 540545CrossRefGoogle ScholarPubMed
Bray, GAAfferent signals regulating food intake. Proc Nutr Soc (2000) 59, 373384CrossRefGoogle ScholarPubMed
Curhan, GC, Chertow, GM, Willett, WC, Spiegelman, D, Colditz, GA, Manson, JE, Speizer, FE & Stampfer, MJBirth weight and adult hypertension and obesity in women. Circulation (1996) 94, 13101315CrossRefGoogle ScholarPubMed
Dahri, S, Snoeck, A, Reusens-Billen, B, Remacle, C & Hoet, JJIslet function in offspring of mothers on low protein diet during gestation. Diabetes (1991) 40, 115120CrossRefGoogle ScholarPubMed
Eriksson, JG, Forsen, TJ, Osmond, C & Barker, DJPathways of infant and childhood growth that lead to type 2 diabetes. Diabetes Care (2003) 26, 30063010CrossRefGoogle ScholarPubMed
Gambling, L, Dunford, S, Wallace, DI, Zuur, G, Solanky, N, Srai, SK & McArdle, HIron deficiency during pregnancy affects postnatal blood pressure in the rat. J Physiol (2003) 552, 603610CrossRefGoogle ScholarPubMed
Huxley, R, Neil, A & Collins, RUnravelling the fetal origins hypothesis: is there really an inverse association between birthweight and subsequent blood pressure? Lancet (2002) 360, 659665CrossRefGoogle ScholarPubMed
Jones, AP & Friedman, MIObesity and adipocyte abnormalities in offspring of rats undernourished during pregnancy. Science (1982) 215, 15181519CrossRefGoogle ScholarPubMed
Jones, AP, Simson, EL & Friedman, MIGestational undernutrition and the development of obesity in rats. J Nutr (1983) 114, 14821484Google Scholar
Kanarek, RB & Hirsch, EDietary induced over-eating in experimental animals. Fed Proc (1977) 36, 154158Google ScholarPubMed
Langley, SC & York, DAThe effects of the antiglucocorticoid RU486 on the development of obesity in the obese fa/fa Zucker rat. Am J Physiol (1990) 259, R539R542Google Scholar
Langley-Evans, SCCritical differences between two low protein diet protocols in the programming of hypertension in the rat. Int J Food Sci Nutr (2000) 51, 1117CrossRefGoogle ScholarPubMed
Langley-Evans, SCFetal programming of cardiovascular function through exposure to maternal undernutrition. Proc Nutr Soc (2001) 60, 505513CrossRefGoogle ScholarPubMed
Langley-Evans, SC, Bellinger, L, Sculley, DV, Langley-Evans, AJ & McMullen, SManipulation of the maternal diet in rat pregnancy: different approaches to the demonstration of the programming principle. In Early Life Origins of Adult Health and Disease, [Wintour-Coghlan, M and Owens, JA, editors]. Georgetown: Landes Biosciences Publishing (In the Press). (2004)Google Scholar
Langley-Evans, SC, Makinson, O & McMullen, SRenal programming by maternal low protein diets in the rat is not related to dietary methionine content. Pediatr Res (2003) 53, P402Google Scholar
Langley-Evans, SC, Phillips, GJ & Jackson, AAIn utero exposure to maternal low protein diets induces hypertension in weanling rats, independently of maternal blood pressure changes. Clin Nutr (1994) 13, 319324CrossRefGoogle ScholarPubMed
Langley-Evans, SC, Welham, SJM, Sherman, RC & Jackson, AAWeanling rats exposed to maternal low protein diets during discrete periods of gestation exhibit differing severity of hypertension. Clin Sci (1996) 91, 607615CrossRefGoogle ScholarPubMed
Law, CM, Barker, DJP, Osmond, C, Fall, CHD & Simmonds, SJEarly growth and abdominal fatness in adult life. J Epidemiol Community Health (1992) 46, 184186CrossRefGoogle ScholarPubMed
McCarthy, HD, Pickard, CL, Speed, J & Jackson, AASexual dimorphism of macronutrient selection and regional adipose tissue accumulation following in utero exposure to maternal low protein diet. Proc Nutr Soc (1994) 53, 172AGoogle Scholar
Martorell, R, Stein, AD & Schroeder, DGEarly nutrition and later adiposity. J Nutr (2001) 131, 874S880SCrossRefGoogle ScholarPubMed
Paz, I, Seidman, DS, Danon, YL, Laor, A, Stevenson, DK & Gale, RAre children born small-for-gestational-age at increased risk of short stature? Am J Dis Child (1993) 147, 337339Google ScholarPubMed
Petry, CJ, Ozanne, SE, Wang, CL & Hales, CNEarly protein restriction and obesity independently induce hypertension in year old rats. Clin Sci (1997) 93, 147152CrossRefGoogle ScholarPubMed
Petry, CJ, Dorling, MW, Pawlak, DB, Ozanne, SE & Hales, CNDiabetes in male offspring of rat dams fed a reduced protein diet. Int J Exp Diabetes Res (2001) 2, 139143CrossRefGoogle ScholarPubMed
Plagemann, A, Harder, T, Rake, A, Melchior, K, Rohde, W &Dorner, GHypothalamic nuclei are malformed in weanling offspring of low protein malnourished rat dams. J Nutr (2000) 130, 25822589CrossRefGoogle ScholarPubMed
Ravelli, AC, van der Meulen, JH, Osmond, C, Barker, DJ & Bleker, OPObesity at the age of 50 y in men and women exposed to famine prenatally. Am J Clin Nutr (1999) 70, 811816CrossRefGoogle ScholarPubMed
Ravelli, G, Stein, Z & Susser, MWObesity in young men after famine exposure in utero and in early infancy. New Engl J Med (1976) 295, 349353CrossRefGoogle ScholarPubMed
Rees, WDManipulating the sulfur amino acid content of the early diet and its implications for long-term health. Proc Nutr Soc (2002) 61, 7177CrossRefGoogle ScholarPubMed
Rothwell, NJ & Stock, MJEffects of feeding a palatable "cafeteria" diet on energy balance on young and adult lean (+/?) Zucker rats. Br J Nutr (1982) 47, 461471CrossRefGoogle Scholar
Sakai, N & Imada, SBilateral lesions of the insular cortex or of the prefrontal cortex block the association between taste and odor in the rat. Neurobiol Learn Mem (2003) 80, 2431CrossRefGoogle ScholarPubMed
Valdez, R, Athens, MA, Thompson, GH, Bradshaw, BS & Stern, MPBirthweight and adult health outcomes in a biethnic population in the USA. Diabetologia (1994) 37, 627631CrossRefGoogle Scholar
Vehaskari, VM, Aviles, DH & Manning, JPrenatal programming of adult hypertension in the rat. Kidney Int (2001) 59, 238245CrossRefGoogle ScholarPubMed
Vickers, MH, Breier, BH, Cutfield, WS, Hofman, PL & Gluckman, PDFetal origins of hyperphagia, obesity, and hypertension and postnatal amplification by hypercaloric nutrition. Am J Physiol Endocrinol Metab (2000) 279, E83E87CrossRefGoogle ScholarPubMed
Vickers, MH, Breier, BH, McCarthy, D & Gluckman, PDSedentary behavior during postnatal life is determined by the prenatal environment and exacerbated by postnatal hypercaloric nutrition. Am J Physiol (2003) 285, R271R273Google ScholarPubMed
Woods, LL, Weeks, DA & Rasch, RProgramming of adult blood pressure by maternal protein restriction: Role of nephrogenesis. Kidney Int (2004) 65, 13391348CrossRefGoogle ScholarPubMed