![]() |
|
|
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||

* Rowett Research Institute, Bucksburn, Aberdeen, AB21 9SB UK and
Biomathematics and Statistics Scotland, Rowett Research Institute, Bucksburn, Aberdeen, AB21 9SB UK
2 To whom correspondence should be addressed. E-mail: H.McArdle{at}rowett.ac.uk.
Imbalances in nutrition during pregnancy can lead to long-, as well as short-term consequences, a phenomenon known as fetal programming. However, there is little information about when the fetus is most sensitive to its environment during gestation. We hypothesize that different fetal systems are most vulnerable to nutritional stress during periods of maximal growth and differentiation. We used iron (Fe) deficiency, which causes hypertension in the offspring, to test this hypothesis. We examined development between embryonic day (E) 10.5 and 12.5, when cardiovascular development is maximal, using whole embryo culture. Female rats were fed Fe-deficient or control diet for 4 wk before mating and up to E10.5. The embryos were cultured for 48 h in 95% rat serum collected from males fed either a control or Fe-deficient diet. Growth was impaired and heart size increased in embryos taken from Fe-deficient mothers and cultured in deficient serum compared with control embryos cultured in control serum. To test whether restoring normal Fe levels could reverse these effects, we cultured embryos from control and deficient dams in either control or deficient medium. The yolk sac circulation of embryos from dams fed either diet cultured in deficient medium was less developed, with a thinner and less branched network than that in all embryos cultured in control serum. The heart was enlarged in embryos of deficient dams cultured in deficient serum compared with the heart size of those cultured in control serum. Culturing embryos in control serum reversed these changes. We conclude, therefore, that this period of cardiovascular organogenesis is one of the sensitive windows during which optimal Fe status is critical for normal development.
KEY WORDS: fetal programming developmental origins embryo culture micronutrients
This article has been cited by other articles:
![]() |
C. P. Stewart, P. Christian, K. J. Schulze, S. C. LeClerq, K. P. West Jr, and S. K. Khatry Antenatal Micronutrient Supplementation Reduces Metabolic Syndrome in 6- to 8-Year-Old Children in Rural Nepal J. Nutr., August 1, 2009; 139(8): 1575 - 1581. [Abstract] [Full Text] [PDF] |
||||
![]() |
I. Cetin, C. Berti, and S. Calabrese Role of micronutrients in the periconceptional period Hum. Reprod. Update, June 30, 2009; (2009) dmp025v1. [Abstract] [Full Text] [PDF] |
||||
![]() |
Z. Wang, Z. Huang, G. Lu, L. Lin, and M. Ferrari Hypoxia during pregnancy in rats leads to early morphological changes of atherosclerosis in adult offspring Am J Physiol Heart Circ Physiol, May 1, 2009; 296(5): H1321 - H1328. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. Gambling, A. Czopek, H. S. Andersen, G. Holtrop, S. K. S. Srai, Z. Krejpcio, and H. J. McArdle Fetal iron status regulates maternal iron metabolism during pregnancy in the rat Am J Physiol Regulatory Integrative Comp Physiol, April 1, 2009; 296(4): R1063 - R1070. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. L. Bourque, M. Komolova, K. Nakatsu, and M. A. Adams Long-Term Circulatory Consequences of Perinatal Iron Deficiency in Male Wistar Rats Hypertension, January 1, 2008; 51(1): 154 - 159. [Abstract] [Full Text] [PDF] |
||||
![]() |
J. L. Beard, E. L. Unger, L. E. Bianco, T. Paul, S. E. Rundle, and B. C. Jones Early Postnatal Iron Repletion Overcomes Lasting Effects of Gestational Iron Deficiency in Rats J. Nutr., May 1, 2007; 137(5): 1176 - 1182. [Abstract] [Full Text] [PDF] |
||||