Literature DB >> 6360760

Diabetes in pregnancy. Skeletal malformations in the offspring of diabetic rats after intermittent withdrawal of insulin in early gestation.

U J Eriksson, E Dahlström, C Hellerström.   

Abstract

Precise timing of the teratogenic period in diabetic pregnancy is of clinical importance since correction of the glucose intolerance during this period may protect the offspring from malformations. An experimental approach to elucidate this problem with regard to skeletal development was made in groups of pregnant streptozotocin-diabetic rats (MDI), which were treated with daily insulin injections except for a 2-day period in the first half of pregnancy. The degree of metabolic derangement was estimated by measurements of serum glucose concentrations. During the insulin-free period, the rats showed severe hyperglycemia (greater than 20 mM) while during ongoing insulin treatment, only brief periods of hyper- or hypoglycemia were observed. Insulin treatment was withdrawn successively between gestational days 3 and 12. Control groups consisted of normal pregnant rats (N) or pregnant rats with manifest diabetes (MD) without insulin treatment. The serum glucose levels of the N animals were below 6 mM while those of the MD animals were above 25 mM throughout pregnancy. Skeletal malformations in the viable offspring were recorded on gestational day 20 after Alizarin staining of calcified ossification centers, which also allowed an estimate of skeletal development as a whole. Untreated diabetes in the MD rats induced a high rate of fetal resorptions, a decrease in fetal weight and viability, as well as retardation of skeletal development. Intermittent insulin treatment in the MDI rats ameliorated, but did not abolish, these changes. In the MD group 9 of 48 viable fetuses showed severe malformations of either the lower jaw (micrognathia) or of the lumbosacral region (caudal dysgenesis).(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1983        PMID: 6360760     DOI: 10.2337/diab.32.12.1141

Source DB:  PubMed          Journal:  Diabetes        ISSN: 0012-1797            Impact factor:   9.461


  12 in total

Review 1.  Environmental teratogens.

Authors:  R L Brent; D A Beckman
Journal:  Bull N Y Acad Med       Date:  1990 Mar-Apr

2.  Maternal diabetes modulates offspring cell proliferation and apoptosis during odontogenesis via the TLR4/NF-κB signalling pathway.

Authors:  Guoqing Chen; Wenhua Sun; Yan Liang; Tian Chen; Weihua Guo; Weidong Tian
Journal:  Cell Prolif       Date:  2016-12-16       Impact factor: 6.831

3.  Fuel-mediated teratogenesis. Use of D-mannose to modify organogenesis in the rat embryo in vivo.

Authors:  T Buchanan; N Freinkel; N J Lewis; B E Metzger; S Akazawa
Journal:  J Clin Invest       Date:  1985-06       Impact factor: 14.808

4.  In vitro study of the carry-over effect associated with early diabetic embryopathy in the rat.

Authors:  S Pampfer; Y D Wuu; I Vanderheyden; R De Hertogh
Journal:  Diabetologia       Date:  1994-09       Impact factor: 10.122

5.  Skeletal growth of fetuses from streptozotocin diabetic rat mothers: in vivo and in vitro studies.

Authors:  E Heinze; U Vetter
Journal:  Diabetologia       Date:  1987-02       Impact factor: 10.122

Review 6.  Diabetes in pregnancy 1985.

Authors:  D R Hadden
Journal:  Diabetologia       Date:  1986-01       Impact factor: 10.122

7.  Oestrogen and progestogen receptors in endometrium and myometrium at the time of blastocyst implantation in pregnant diabetic rats.

Authors:  R De Hertogh; I Vanderheyden; B Glorieux; E Ekka
Journal:  Diabetologia       Date:  1989-08       Impact factor: 10.122

8.  Effect of maternal diabetes and ethanol interactions on embryo development in the mouse.

Authors:  R Padmanabhan; M Shafiullah
Journal:  Mol Cell Biochem       Date:  2004-06       Impact factor: 3.396

9.  Oxidative stress-induced JNK1/2 activation triggers proapoptotic signaling and apoptosis that leads to diabetic embryopathy.

Authors:  Xuezheng Li; Hongbo Weng; Cheng Xu; E Albert Reece; Peixin Yang
Journal:  Diabetes       Date:  2012-06-11       Impact factor: 9.337

10.  c-Jun NH2-terminal kinase 1/2 and endoplasmic reticulum stress as interdependent and reciprocal causation in diabetic embryopathy.

Authors:  Xuezheng Li; Cheng Xu; Peixin Yang
Journal:  Diabetes       Date:  2012-09-06       Impact factor: 9.461

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