Hostname: page-component-cd9895bd7-dzt6s Total loading time: 0 Render date: 2024-12-28T12:20:00.516Z Has data issue: false hasContentIssue false

The effects of maternal protein restriction on the growth of the rat fetus and its amino acid supply

Published online by Cambridge University Press:  09 March 2007

William D. Rees*
Affiliation:
The Rowett Research Institute, Greenburn Road, Bucksburn, Aberdeen, AB21 9SB, UK
Susan M. Hay
Affiliation:
The Rowett Research Institute, Greenburn Road, Bucksburn, Aberdeen, AB21 9SB, UK
Viv Buchan
Affiliation:
The Rowett Research Institute, Greenburn Road, Bucksburn, Aberdeen, AB21 9SB, UK
Christos Antipatis
Affiliation:
The Rowett Research Institute, Greenburn Road, Bucksburn, Aberdeen, AB21 9SB, UK
Robert M. Palmer
Affiliation:
The Rowett Research Institute, Greenburn Road, Bucksburn, Aberdeen, AB21 9SB, UK
*
*Corresponding author: Dr William D. Rees, fax +44 (0) 1224 715349, 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.

Maternal protein deficiency causes fetal growth retardation which has been associated with the programming of adult disease. The growth of the rat fetus was examined when the mothers were fed on diets containing 180, 90 and 60 g protein/kg. The numbers of fetuses were similar in animals fed on the 180 and 90 g protein/kg diets but the number was significantly reduced in the animals fed on the 60 g protein/kg diet. The fetuses carried by the mothers fed on the 90 g protein/kg diet were 7·5% heavier than those of mothers fed on 180 g protein/kg diet on day 19 of gestation, but by day 21 the situation was reversed and the fetuses in the protein-deficient mothers were 14% smaller. Analysis of the free amino acids in the maternal serum showed that on day 19 the diets containing 90 and 60 g protein/kg led to threonine concentrations that were reduced to 46 and 20% of those found in animals fed on the control (180 g/kg) diet. The other essential amino acids were unchanged, except for a small decrease in the branched-chain amino acids in animals fed on the 60 g protein/kg diet. Both low-protein diets significantly increased the concentrations of glutamic acid+glutamine and glycine in the maternal serum. On day 21 the maternal serum threonine levels were still reduced by about one third in the group fed on the 90 g protein/kg diet. Dietary protein content had no effect on serum threonine concentrations in non-pregnant animals. Analysis of the total free amino acids in the fetuses on day 19 showed that feeding the mother on a low-protein diet did not change amino acid concentrations apart from a decrease in threonine concentrations to 45 and 26% of the control values at 90 and 60 g protein/kg respectively. The results suggest that threonine is of particular importance to the protein-deficient mother and her fetuses. Possible mechanisms for the decrease in free threonine in both mother and fetuses and the consequences of the change in amino acid metabolism are discussed.

Type
Research Article
Copyright
Copyright © The Nutrition Society 1999

References

Adkins, JS, Wertz, JM & Hove, EL (1966) Influence of non-essential amino acids on growth of rats fed high levels of essential amino acids. Proceedings of the Society for Experimental Biology and Medicine 122, 519523.CrossRefGoogle Scholar
Ashford, AJ & Pain, VM (1986) Effect of diabetes on the rates of synthesis and degradation of ribosomes in rat muscle and liver in vivo. Journal of Biological Chemistry 261, 40594065.Google Scholar
Bakker, RC & Brandjes, DPM (1997) Hyperhomocysteinaemia and associated disease. Pharmacy World and Science 19, 126132.Google Scholar
Ballevre, O, Cadenhead, A, Calder, AG, Rees, WD, Lobley, GE, Fuller, MF & Garlick, PJ (1990) Quantitative partition of threonine oxidation in pigs: effect of dietary threonine. American Journal of Physiology 259, E483E491.Google ScholarPubMed
Barker, DJ (1995) Fetal origins of coronary heart disease. British Medical Journal 311, 171174.Google Scholar
Bird, MI & Nunn, PB (1983) Metabolic homeostasis of l-threonine in the normally fed rat. Importance of liver threonine dehydrogenase activity. Biochemical Journal 214, 687694.Google Scholar
Burton, K (1956) A study of the conditions and mechanisms of the diphenylamine reaction for the colorimetric estimation of deoxyribonucleic acid. Biochemical Journal 62, 315318.CrossRefGoogle ScholarPubMed
Cherif, H, Reusens, B, Dahri, S, Remacle, C & Hoet, J-J (1996) Stimulatory effects of taurine on insulin secretion by fetal rat islets cultured in vitro. Journal of Endocrinology 151, 501506.Google Scholar
Davison, AN & Dobbing, J (1966) Myelination as a vulnerable period in brain development. British Medical Bulletin 22, 4044.Google Scholar
Desai, M, Crowther, NJ, Lucas, A & Hales, CN (1996) Organ-selective growth in the offspring of protein-restricted mothers. British Journal of Nutrition 76, 591603.Google Scholar
Desai, M, Crowther, NJ, Ozanne, SE, Lucas, A & Hales, CN (1995) Adult glucose and lipid metabolism may be programmed during fetal life. Biochemical Society Transactions 23, 331335.CrossRefGoogle ScholarPubMed
Fleming, JV, Hay, SM, Harries, DN & Rees, WD (1998) The effects of nutrient deprivation and differentiation on the expression of growth arrest genes (gas and gadd) in F9 embryonal carcinoma cells. Biochemical Journal 330, 573579.CrossRefGoogle ScholarPubMed
Gaull, GE, von Berg, W, Raiha, NCR & Sturman, JA (1973) Development of methyltransferase activities of human fetal tissues. Pediatric Research 7, 527533.Google Scholar
Girard-Globa, A, Robin, P & Forestier, M (1972) Long-term adaptation of weanling rats to high dietary levels of methionine and serine. Journal of Nutrition 102, 209218.Google Scholar
Godfrey, KM, Forrester, T, Barker, DJ, Jackson, AA, Landman, JP, Hall, JS, Cox, V & Osmond, C (1994) Maternal nutritional status in pregnancy and blood pressure in childhood. British Journal of Obstetrics and Gynaecology 101, 398403.CrossRefGoogle ScholarPubMed
Harper, AE (1974) 'Non essential' amino acids. Journal of Nutrition 104, 965967.Google Scholar
Jackson, AA (1991) The glycine story. European Journal of Clinical Nutrition 45, 5965.Google Scholar
Jackson, AA, Persaud, C, Werkmeister, G, McClelland, ISM, Badaloo, A & Forrester, T (1997) Comparison of urinary 5-l-oxoproline (l-pyroglutamate) during normal pregnancy in women in England and Jamaica. British Journal of Nutrition 80, 5155.Google Scholar
Kang-Lee, YAE & Harper, AE (1978) Threonine metabolism in vivo: effect of threonine intake and prior induction of threonine dehydratase in rats. Journal of Nutrition 108, 163175.Google Scholar
Langley, SC & Jackson, AA (1994) Increased systolic blood pressure in adult rats is altered by in utero exposure to maternal low protein diets. Journal of Nutrition 124, 15881596.Google Scholar
Langley-Evans, SC, Browne, RF & Jackson, AA (1994) Altered glucose tolerance in rats exposed to maternal low protein diets in utero. Comparative Biochemistry and Physiology 109A, 223229.Google Scholar
Langley-Evans, SC, Gardner, DS & Jackson, AA (1996) Association of disproportionate growth of fetal rats with raised systolic blood pressure in later life. Journal of Reproduction and Fertility 106, 307312.Google Scholar
Lenton, C, Ali, Z, Persaud, C & Jackson, AA (1998) Infants in Trinidad excrete more 5-l-oxoproline (l-pyroglutamic acid) in urine than infants in England: an environmental not ethnic difference. British Journal of Nutrition 80, 5155.Google Scholar
Lowry, OH, Rosebrough, NJ, Farr, AL & Randall, RJ (1951) Protein measurement with the Folin phenol reagent. Journal of Biological Chemistry 193, 265272.Google Scholar
Naismith, DJ & Morgan, BLG (1976) The biphasic nature of protein metabolism during pregnancy in the rat. British Journal of Nutrition 36, 563566.Google Scholar
Palmer, RM, Thom, A & Flint, DJ (1996) Repartitioning of maternal muscle protein towards the fetus induced by a polyclonal antiserum to rat GH. Journal of Endocrinology 151, 395400.CrossRefGoogle ScholarPubMed
Phillips, DI, Barker, DJ, Hales, CN, Hirst, S & Osmond, C (1994) Thinness at birth and insulin resistance in adult life. Diabetologia 37, 150154.CrossRefGoogle ScholarPubMed
Remesar, X, Lopex-Tejero, D & Pastor-Anglada, M (1987) Some aspects of amino acid metabolism in the rat fetus. Comparative Biochemistry and Physiology 88B, 719725.Google Scholar
Reusens, B, Dahri, S, Snoeck, A, Bennis-Taleb, N, Remacle, C & Hoet, J-J (1995) Long term consequences of diabetes and its complications may have a fetal origin: experimental and epidemiological evidence. In Diabetes: Nestlé Nutrition Workshop Series, vol. 35, pp. 187198 [Cowett, RM, editor]. New York, NY: Raven Press.Google Scholar
Rowe, PB & McEwen, SE (1983) De novo purine synthesis in cultured rat embryos undergoing organogenesis. Proceedings of the National Academy of Sciences USA 80, 73337336.Google Scholar
Snoeck, A, Remacle, C, Reusens, B & Hoet, JJ (1990) Effect of a low protein diet during pregnancy on the fetal rat endocrine pancreas. Biology of the Neonate 57, 107118.CrossRefGoogle ScholarPubMed
VanAerts, LAGJM, Blom, HJ, DeAbreu, RA, Trijbels, FJM, Eskes, TKAB, Copius, Peereboom-Stegeman JHJC & Noordhoek, J (1994) Prevention of neural tube defects by and toxicity of l-homocysteine in cultured postimplantation rat embryos. Teratology 50, 348360.Google Scholar
VanAerts, LAGJMPoirot, CM, Herberts, CA, Blom, HJ, DeAbreu, RA, Trijbels, FJM, Eskes, TKAB, Copius, Peereboom-Stegeman JHJC & Noordhoek, J (1995) Development of methionine synthase, cystathionine-b-synthase and S-adenosyl-homocysteine hydrolase during gestation in rats. Journal of Reproduction and Fertility 103, 227232.Google Scholar
Widdowson, EM & McCance, RA (1963) Effects of finite periods of under-nutrition at different ages on the composition and subsequent development of the rat. Proceedings of the Royal Society Series B 158, 329342.Google Scholar
Wouters, MGAJ, Thomas, CMG, Boers, GHJ, Borm, GF, Blom, HJ, Steegers-Theunisen, RPM, Trijbels, FJM & Eskes, TKAB (1993) Hyperhomocysteinemia: a risk factor in women with unexplained recurrent early pregnancy loss. Fertility and Sterility 60, 820825.Google Scholar