uu.seUppsala University Publications
Change search
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf
Congenital malformations in experimental diabetic pregnancy: Aetiology and antioxidative treatment
Uppsala University, Medicinska vetenskapsområdet, Faculty of Medicine, Department of Medical Cell Biology.
1997 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

Diabetes mellitus in pregnancy causes congenital malformations in the offspring.The aim of this work was to characterize biochemical and morphologic anomaliesin the conceptus of an animal model of diabetic pregnancy. In addition, apreventive treatment against diabetes-induced dysmorphogenesis was developed.Congenital cataract was often found in the offspring of diabetic rats. The fetal lenseshad increased water accumulation, sorbitol concentration and aldose reductaseactivity compared to control lenses. The results suggest that the cataracts form viaosmotic attraction of water due to sorbitol accumulation in the fetal lens.

Another set of malformations, with possible neural crest cell origin, occurredfrequently in offspring of diabetic rats. These included low set ears, micrognathia,hypoplasia of the thymus, thyroid and parathyroid glands, as well as anomalies ofthe heart and great vessels. Furthermore, diabetes caused intrauterine death andresorptions more frequently in the late part of gestation.

When the pregnant diabetic rats were treated with the antioxidants butylatedhydroxytoluene, vitamin E or vitamin C, the occurrence of gross malformationswas reduced from approximately 25% to less than 8%, and late resorptions from17% to 7%. This suggests that an abnormal handling of reactive oxygen species(ROS) is involved in diabetes-induced dysmorphogenesis in vivo. Indeed, anincreased concentration of lipid peroxides, indicating damage caused by ROS, wasfound in fetuses of diabetes rats. In addition, embryos of diabetic rats had lowconcentrations of the antioxidant vitamin E compared to control embryos. Thesebiochemical alterations were normalized by vitamin E treatment of the pregnantdiabetic rats.

The antioxidants are likely to have prevented ROS injury in the embryos of thediabetic rats, in particular in the neural crest cells, thereby normalizing embryonicdevelopment. These results provide a rationale for developing new anti-teratogenictreatments for pregnant women with diabetes mellitus.

Place, publisher, year, edition, pages
Uppsala: Acta Universitatis Upsaliensis , 1997. , 55 p.
Series
Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine, ISSN 0282-7476 ; 704
Keyword [en]
Cell biology, Diabetes, pregnancy, teratology, malformations, embryo, fetus, cataract, sorbitol, antioxidants, butylated hydroxytoluene, vitamin E, vitamin C, TBARS, neural crest cells
Keyword [sv]
Cellbiologi
National Category
Cell and Molecular Biology
Research subject
Medical Cell Biology
Identifiers
URN: urn:nbn:se:uu:diva-116ISBN: 91-554-4023-1 (print)OAI: oai:DiVA.org:uu-116DiVA: diva2:160710
Public defence
1997-09-19, lecture hall B21, Uppsala Biomedical Centre, Uppsala University, Uppsala, 09:15
Available from: 1997-08-29 Created: 1997-08-29Bibliographically approved

Open Access in DiVA

No full text
Buy this publication >>

By organisation
Department of Medical Cell Biology
Cell and Molecular Biology

Search outside of DiVA

GoogleGoogle Scholar

isbn
urn-nbn

Altmetric score

isbn
urn-nbn
Total: 671 hits
CiteExportLink to record
Permanent link

Direct link
Cite
Citation style
  • apa
  • ieee
  • modern-language-association
  • vancouver
  • Other style
More styles
Language
  • de-DE
  • en-GB
  • en-US
  • fi-FI
  • nn-NO
  • nn-NB
  • sv-SE
  • Other locale
More languages
Output format
  • html
  • text
  • asciidoc
  • rtf