Prenatal Exposure to a Maternal Low Protein Diet Shortens Life Span in Rats

Background: Postweaning diet restriction is associated with prolongation of life span, reduced age-related disease and slower ageing. The effects of diet restriction imposed prior to weaning have not been so well characterised, but studies suggest an opposite effect with increased age-related diseases occurring in offspring exposed to undernutrition in prenatal life. It remains unclear whether life span is similarly adversely affected by early diet restriction. Objective: The present study in rats aimed to evaluate the impact of a maternal low protein diet upon the life span of the resulting offspring. Methods: Rat dams were fed either a 180-gram casein/kg control diet or a 90-gram casein/kg low protein diet from conception until the end of pregnancy. The offspring were then maintained with minimal handling until death from natural causes or distress-necessitated euthanasia. Results: The average life span of female rats exposed to low protein diets in utero was reduced by 11% (p = 0.044, Kaplan-Meier analysis). There was a similar but non- significant trend in the male offspring (control 76 ± 3 weeks, low protein 73 ± 3 weeks). In addition the rats exposed to a prenatal low protein diet had significantly higher systolic blood pressure at 4 weeks of age and tended to be smaller than control animals in postnatal life. Conclusion: The results suggest that intrauterine diet restriction reduces life span in rats and contrasts with the well-recognised increase in life span produced by postweaning diet restriction. The timing of the nutritional intervention appears to be critical and recognition of this is relevant to understanding the mechanisms underlying the effects of diet restriction on ageing and life span.

[1]  C Osmond,et al.  Maternal nutrition in early and late pregnancy in relation to placental and fetal growth , 1996, BMJ.

[2]  A Lucas,et al.  Programming by early nutrition in man. , 2007, Ciba Foundation symposium.

[3]  B. J. Jennings,et al.  Early growth determines longevity in male rats and may be related to telomere shortening in the kidney , 1999, FEBS letters.

[4]  C Osmond,et al.  Initiation of hypertension in utero and its amplification throughout life. , 1993, BMJ.

[5]  D J Barker,et al.  Diet in pregnancy and the offspring's blood pressure 40 years later , 1996, British journal of obstetrics and gynaecology.

[6]  C. Barrows The Effect of Dietary Restriction on Life Span , 1989 .

[7]  S. Langley-Evans,et al.  Evidence of progressive deterioration of renal function in rats exposed to a maternal low-protein diet in utero , 2000, British Journal of Nutrition.

[8]  C. Cooper,et al.  Are rates of ageing determined in utero? , 1998, Age and ageing.

[9]  D. Gardner,et al.  Association of disproportionate growth of fetal rats in late gestation with raised systolic blood pressure in later life. , 1996, Journal of reproduction and fertility.

[10]  C. Lee,et al.  EFFECT OF DIETARY RESTRICTION OF PREGNANT RATS ON BODY WEIGHT GAIN OF THE OFFSPRING. , 1964, The Journal of nutrition.

[11]  C. Cooper,et al.  Undernutrition and aging. , 1997, Gerontology.

[12]  A. Kahn Embryogenic effect on post-natal changes in hemoglobin concentration with time. , 1968, Growth.

[13]  Simon J. M. Welham,et al.  Fetal exposure to a maternal low protein diet impairs nephrogenesis and promotes hypertension in the rat. , 1999, Life sciences.

[14]  S. Ozanne,et al.  Early protein restriction and obesity independently induce hypertension in 1-year-old rats. , 1997, Clinical science.

[15]  S. Langley-Evans,et al.  Early administration of angiotensin-converting enzyme inhibitor captopril, prevents the development of hypertension programmed by intrauterine exposure to a maternal low-protein diet in the rat. , 1998, Clinical science.

[16]  A. Jackson,et al.  Increased systolic blood pressure in adult rats induced by fetal exposure to maternal low protein diets. , 1994, Clinical science.

[17]  Kahn Aj Embryogenic effect on post-natal changes in hemoglobin concentration with time. , 1968 .

[18]  C Osmond,et al.  Fetal and infant growth and impaired glucose tolerance at age 64. , 1991, BMJ.

[19]  S. Ozanne,et al.  Fishing in the stream of diabetes: from measuring insulin to the control of fetal organogenesis. , 1996, Biochemical Society transactions.

[20]  D. Ingram,et al.  Slowing ageing by caloric restriction , 1995, Nature Medicine.

[21]  T. B. Robertson,et al.  EXPERIMENTAL STUDIES ON GROWTH XV. ON THE GROWTH OF RELATIVELY LONG LIVED COMPARED WITH THAT OF RELATIVELY SHORT LIVED ANIMALS , 1920 .

[22]  D J Barker,et al.  Is lifespan determined in utero? , 1997, Archives of disease in childhood. Fetal and neonatal edition.

[23]  D. Barker,et al.  Weight in infancy and prevalence of coronary heart disease in adult life , 1995, BMJ.

[24]  S. Langley-Evans,et al.  Impaired growth and increased glucocorticoid-sensitive enzyme activities in tissues of rat fetuses exposed to maternal low protein diets. , 1998, Life sciences.

[25]  P. Egger,et al.  Childhood growth, physical activity, and peak bone mass in women , 1995, Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research.

[26]  Simon J. M. Welham,et al.  Weanling rats exposed to maternal low-protein diets during discrete periods of gestation exhibit differing severity of hypertension. , 1996, Clinical science.

[27]  B. Merry Effect of dietary restriction on lifespan , 1991 .

[28]  R. Grimble,et al.  The acute phase response of adult rats is altered by in utero exposure to maternal low protein diets. , 1994, The Journal of nutrition.