Hostname: page-component-cd9895bd7-jkksz Total loading time: 0 Render date: 2024-12-25T17:24:43.089Z Has data issue: false hasContentIssue false

Some metabolic effects on lactating rats of a low-energy diet restricted in good-quality protein

Published online by Cambridge University Press:  08 March 2007

María del Rosario Ayala
Affiliation:
Departamento de Fisiología Dr Mauricio Russek, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Carpio y Plan de Ayala, Mexico
Radu Racotta
Affiliation:
Departamento de Fisiología Dr Mauricio Russek, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Carpio y Plan de Ayala, Mexico
Homero Hernández-Montes
Affiliation:
Laboratorio de Investigación Médica en Nutrición, Centro Médico Nacional Siglo XXI, IMSS, Mexico
Lucía Quevedo*
Affiliation:
Departamento de Fisiología Dr Mauricio Russek, Escuela Nacional de Ciencias Biológicas, Instituto Politécnico Nacional, Carpio y Plan de Ayala, Mexico
*
*Corresponding author: Dr Lucía Quevedo, fax +52 (55) 57296206, email quevedocorona@hotmail.com
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.

Adult female Sprague–Dawley rats were fed ad libitum during pregnancy and lactation a control diet (CD; 16·1 kJ/g) or a low-energy diet with wheat gluten as the main protein source (LED; 13·3 kJ/g). Body weight, food intake, resting energy expenditure, respiratory quotient and substrate use by the mammary gland were measured. After the animals had been killed, the parametrial and retroperitoneal fat pads were weighed. The mean food intake (g) of the two groups of rats was similar, resulting in a lower energy intake by the LED rats, significantly different during the last 2 weeks of lactation. The mean body weight of both dams and pups in the LED group was lower, starting at day 9 of lactation. The resting energy expenditure increased gradually during lactation in the control group, whereas this increase was not seen in rats of the LED group in the last week of lactation. Rats that had fasted overnight had a respiratory quotient of 0·7 or less, whereas for rats that had been fed, the mean respiratory quotient was over 1·0. Under both conditions, rats showed ketonuria. The arteriovenous difference in 3-hydroxybutyrate level was higher and those for glucose, lactate and triacylglycerol were lower across the mammary glands of LED rats. The parametrial fat depot weighed less in LED rats. Reducing the increase in resting energy expenditure and using ketone bodies to a greater extent as fuels may represent important mechanisms in the LED dams to cover the energy cost of milk production.

Type
Research Article
Copyright
Copyright © The Nutrition Society 2006

References

Blaxter, K (1989) Energy Metabolism in Animals and Man.Cambridge, UK:Cambridge University Press.Google Scholar
Broady, S (1945) Bioenergetics and Growth, New York: Reinhold Publishing.Google Scholar
Butte, NF, Villalpando, S, Wong, WW, Flores-Huerta, S, Hernández-Beltrán, MJ, O'Brian, E (1993) Higher total energy expenditure contributes to growth faltering in breast-fed infants living in rural Mexico. J Nutr 123, 10281035.Google ScholarPubMed
Calloway, DH & Kretsch, MJ (1978) Protein and energy utilization in men given a rural Guatemalean diet and egg formulas with and without added oat bran. Am J Clin Nutr 31, 11181126.CrossRefGoogle Scholar
Del Prado, M, Delgado, D & Villalpando, S (1997) Maternal lipid intake during pregnancy and lactation alters milk composition and production and litter growth in rats. J Nutr 127, 458462.CrossRefGoogle ScholarPubMed
Hellerstein, MK, Schwartz, J-M & Neese, RA (1996) Regulation of hepatic de novo lipogenesis in humans. Annu Rev Nutr 16, 523527.CrossRefGoogle ScholarPubMed
Leon, M & Woodside, B (1983) Energetic limits on reproduction: maternal food intake. Physiol Behav 30, 945957.CrossRefGoogle ScholarPubMed
Quek, VS & Trayhurn, P (1990) Calorimetric study of the energetics of pregnancy in golden hamsters. Am J Physiol 259, R807R812.Google ScholarPubMed
Reeves, PG (1997) Components of the AIN-93 diets as improvements in the AIN-76A diet. J Nutr 127, Suppl. 5, 838s841sCrossRefGoogle ScholarPubMed
Roberts, SB & Coward, WA (1984) Lactation increases the efficiency of energy utilization in rats. J Nutr 114, 21932200.CrossRefGoogle ScholarPubMed
Robinson, AM, Girard, JR & Williamson, D (1978) Evidence for a role of insulin in the regulation of lipogenesis in lactating rat mammary gland. Measurements of lipogenesis in vivo and plasma hormone concentrations in response to starvation and refeeding. Biochem J 176, 343346.CrossRefGoogle ScholarPubMed
Robinson, AM & Williamson, DH (1978) Utilization of D-3-hydroxy[3-14C]butyrate for lipogenesis in vivo in lactating rat mammary gland. Biochem J 176, 635638.CrossRefGoogle ScholarPubMed
Robinson, AM & Williamson, DH (1980) Physiological roles of ketone bodies as substrates and signals in mammalian tissues. Physiol Rev 60, 143187.CrossRefGoogle ScholarPubMed
Rosado, JL, López, P, Morales, M, Muñoz, E & Allen, LH (1992) Bioavailability of energy, nitrogen, fat, zinc, iron and calcium from rural and urban Mexican diets. Br J Nutr 68, 4558.CrossRefGoogle ScholarPubMed
Schutz, Y, Lechtig, A & Bradfield, RB (1980) Energy expenditures and food intakes of lactating women in Guatemala. Am J Clin Nutr 33, 892902.CrossRefGoogle ScholarPubMed
Simonson, DC & DeFronzo, RA (1990) Indirect calorimetry: methodological and interpretative problems. Am J Physiol 258, E399E412.Google ScholarPubMed
Sohlström, A, Kabir, N, Sadurskis, A & Forsum, E (1994) Body composition and fat distribution during the first 2 weeks of gestation in ad lib.-fed and energy-restricted rats. Br J Nutr 71, 317333.CrossRefGoogle ScholarPubMed
Taylor, JB, Calvert, CC, Baldwin, RL & Sainz, RD (1986) Effects of dietary protein, fat and restriction on body composition and energy balance in lactating rats. J Nutr 116, 15191528.CrossRefGoogle ScholarPubMed
Trayhurn, P (1989) Thermogenesis and the energetics of pregnancy and lactation. Can J Physiol Pharmacol 67, 370375.CrossRefGoogle ScholarPubMed
Villanueva, I, Piñon, M, Quevedo-Corona, L, Martínez-Olivares, R & Racotta, R (2002) Chemical sympathectomy alters food intake and thermogenic responses to catecholamines in rats. Life Sci 71, 789801.CrossRefGoogle ScholarPubMed
Viña, JR, Puertes, IR, Rodriguez, A, Saez, GT, Viña, J (1987) Effect of fasting on amino acid metabolism by lactating mammary gland. J Nutr 117, 533538.CrossRefGoogle ScholarPubMed
Whitelaw, E & Williamson, DH (1977) Effects of lactation on ketogenesis from oleate or butyrate in rat hepatocytes. Biochem J 164, 521528.CrossRefGoogle ScholarPubMed
Williamson, DH (1990) The lactating mammary gland of the rat and the starved-refed transition: a model system for the study of the temporal regulation of substrate utilization. Biochem Soc Trans 18, 853856.CrossRefGoogle Scholar
Williamson, DH, Munday, MR & Jones, RG (1984) Biochemical basis of dietary influences on the synthesis of the macronutrients of rat milk. Fed Proc 43, 24432447.Google ScholarPubMed