The risk of congenital abnormality in diabetic pregnancy is about four times that for the normal population. Past clinical studies have suggested hyperglycemia and hyperketonemia as the factors responsible for these abnormalities, with no reference to the possible effects of low insulin levels. We examine the effect of hypoinsulinemia on rat embryonic growth and development in culture while normal glucose levels are maintained. With anti-insulin antibody bound to an affinity column containing cyanogen bromide-activated Sepharose 4B beads, insulin was selectively removed from the homologous culture serum eluted down the column. A culture of rat embryos from the early head-fold stage for 50 h in insulin-depleted normoglycemic homologous serum (insulin levels 0.055–0.18 ng/ml) showed retardation of growth and development when compared with control embryos. Adding physiological amounts (10 ng/ml) of insulin back into the insulin-depleted serum subsequently restored growth level to that of control embryos. We conclude that low insulin levels, encountered in newly diagnosed diabetic pregnancy, may be instrumental in increasing the risk of congenital abnormalities.
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Original Articles|
June 01 1989
Effects of Low Insulin Levels on Rat Embryonic Growth and Development
James P Travers;
James P Travers
Department of Anatomy, University of Leicester
Leicester, United Kingdom
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Margaret K Pratten;
Margaret K Pratten
Department of Anatomy, University of Leicester
Leicester, United Kingdom
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Felix Beck
Felix Beck
Department of Anatomy, University of Leicester
Leicester, United Kingdom
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Address correspondence and reprint requests to Dr. James P. Travers, Department of Human Morphology, Queen's Medical Centre, Clifton Boulevard, University of Nottingham, Nottingham NG-7 2UH, UK.
Diabetes 1989;38(6):773–778
Article history
Received:
May 17 1988
Revision Received:
February 13 1989
Accepted:
February 13 1989
PubMed:
2656345
Citation
James P Travers, Margaret K Pratten, Felix Beck; Effects of Low Insulin Levels on Rat Embryonic Growth and Development. Diabetes 1 June 1989; 38 (6): 773–778. https://doi.org/10.2337/diab.38.6.773
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