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Effect of Diabetes on Circulating Pancreatic Hormones in Pregnant Rats and Their Offspring
I L Iessi1, Y K Sinzato1, F Q Gallego1
1Laboratory of Experimental Research in Gynecology and Obstetrics, Program of Gynecology, Obstetrics and Mastology Graduate Course, Botucatu Medical School, Unesp Univ Estadual Paulista, Botucatu, São Paulo State, Brazil.
Insights
Maternal diabetes during pregnancy alters pancreatic hormone levels in mothers, fetuses, and offspring. This study reveals how diabetes impacts insulin, glucagon, and somatostatin in a diabetic rat model.
Area of Science:
- Endocrinology
- Reproductive Biology
- Metabolic Disorders
Background:
- The intrauterine environment significantly influences fetal development and long-term health.
- Maternal diabetes can lead to fetal growth abnormalities and metabolic dysregulation.
- Pancreatic hormones like insulin, glucagon, and somatostatin play critical roles in glucose homeostasis.
Purpose of the Study:
- To investigate the impact of a diabetic intrauterine environment on circulating levels of insulin, glucagon, and somatostatin.
- To examine these hormonal changes in pregnant rats (dams), their fetuses, and offspring.
- To understand the role of streptozotocin-induced diabetes in altering pancreatic hormone profiles across generations.
Main Methods:
- Induction of diabetes in Wistar rats using streptozotocin at birth or adulthood.
- Categorization of rats into control, mildly diabetic (MD), and severely diabetic (SD) groups.
- Assessment of dams, fetuses (day 21 pregnancy), and offspring (day 10 postpartum) for hormonal levels and glucose tolerance.
Main Results:
- Severely diabetic (SD) dams exhibited impaired glucose tolerance, lower body weight, and reduced insulin levels.
- SD fetuses showed hyperglycemia with decreased insulin and glucagon.
- SD newborns had diminished pancreatic insulin and plasma somatostatin; mildly diabetic (MD) groups displayed lower glucagon and somatostatin levels.
- MD offspring maintained lower somatostatin levels into the neonatal period.
Conclusions:
- A diabetic intrauterine environment profoundly alters circulating pancreatic hormone levels in dams, fetuses, and offspring.
- Gestational diabetes can lead to persistent hormonal imbalances affecting offspring's metabolic programming.
- These findings highlight the critical role of maternal metabolic health in offspring development and endocrine function.
Abstract:
The aim of the study was to investigate the role of diabetic intrauterine environment on circulating insulin, glucagon, and somatostatin levels in pregnant rats, fetuses, and offspring. Diabetes was induced in female Wistar rats by streptozotocin at birth or as adult and the animals were assigned into: control (C); mildly diabetic (MD); and severely diabetic (SD). The rats were mated and distributed into 2 subgroups: euthanasia at day 21 of pregnancy and at day 10 postpartum. Both MD and SD dams showed impaired oral glucose tolerance. SD dams had lower body weight and insulin levels compared to C and MD dams. SD fetuses presented hyperglycemia and reduction of insulin and glucagon levels compared to C and MD fetuses. SD newborns had diminished total pancreatic insulin and plasma somatostatin compared to the other groups. MD dams and fetuses had lower glucagon and somatostatin levels compared to C dams. MD offspring had maintained lower somatostatin levels to neonatal period. Diabetes causes alterations in circulating levels of pancreatic hormones in the mother and offspring.
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