Impairment of Rat Fetal Beta-Cell Development by Maternal Exposure to Dexamethasone during Different Time-Windows
2011

Impact of Dexamethasone on Fetal Pancreas Development

Sample size: 45 publication 10 minutes Evidence: moderate

Author Information

Author(s): Dumortier Olivier, Theys Nicolas, Ahn Marie-Thérèse, Remacle Claude, Reusens Brigitte

Primary Institution: Laboratoire de Biologie Cellulaire, Université catholique de Louvain, Institut des Sciences de la Vie, Louvain-la-Neuve, Belgium

Hypothesis

This study aims to investigate the consequences of overexposure to exogenous glucocorticoids during different time-windows of gestation for the development of the fetal endocrine pancreas.

Conclusion

Excessive glucocorticoid levels during gestation reduce the beta- and alpha-cell mass in the pancreas through different mechanisms depending on the timing of exposure.

Supporting Evidence

  • Dexamethasone reduced beta-cell mass by 62% when given throughout gestation.
  • Fetuses exposed to glucocorticoids had reduced insulin secretion.
  • Islet vascularization was significantly decreased in fetuses exposed to dexamethasone throughout gestation.

Takeaway

Giving too much of a stress hormone called dexamethasone to pregnant rats can hurt the growth of their babies' pancreas, which is important for making insulin.

Methodology

Pregnant Wistar rats were given dexamethasone in their drinking water during different gestational periods, and the fetuses were analyzed for pancreatic development.

Potential Biases

Potential bias in the selection of treatment groups and the interpretation of results.

Limitations

The study was conducted on rats, which may not fully represent human responses to glucocorticoid exposure.

Participant Demographics

Pregnant Wistar rats were used in the study.

Statistical Information

P-Value

p<0.05

Statistical Significance

p<0.05

Digital Object Identifier (DOI)

10.1371/journal.pone.0025576

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