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Sex differences in offspring neurodevelopment, cognitive performance and microglia morphology associated with
Fábio J Sousa1,2, Raquel G Correia1,2, Alexandra F Cruz1,2
1Coimbra Institute for Clinical and Biomedical Research (iCBR), Faculty of Medicine, University of Coimbra, Coimbra, Portugal.
Insights
Maternal diabetes impacts offspring brain development and behavior, with sex-specific effects. Insulin treatment during pregnancy mitigates most adverse outcomes, highlighting the importance of sex-specific considerations in managing gestational diabetes.
Area of Science:
- Neuroscience
- Developmental Biology
- Immunology
Background:
- Maternal diabetes during pregnancy poses risks to offspring central nervous system (CNS) development, potentially causing cognitive impairment and psychiatric disorders.
- Microglia, the CNS immune cells, are crucial sensors of intrauterine metabolic challenges and actively shape brain development.
- Significant sex dimorphism exists in neurodevelopment and microglial function, necessitating investigation into sex-specific impacts of maternal diabetes.
Purpose of the Study:
- To investigate the sex-specific effects of maternal diabetes on offspring behavior and microglia morphology during infancy.
- To determine if insulin therapy can prevent or mitigate maternal diabetes-induced adverse effects on offspring development and behavior, considering sex differences.
- To analyze molecular and cellular factors in the hippocampus potentially linking metabolic changes to behavioral outcomes.
Main Methods:
- Utilized a rodent model to study the effects of maternal diabetes on offspring development, behavior, and hippocampal microglia morphology.
- Assessed cognitive functions, including recognition memory, and analyzed molecular and cellular markers in the hippocampus.
- Investigated the impact of insulin treatment in diabetic dams on offspring outcomes and microglial characteristics.
Main Results:
- Maternal diabetes globally delayed offspring development and impaired recognition memory specifically in female offspring.
- Sex-specific alterations in molecular and cellular markers were observed in the hippocampus of offspring.
- Insulin treatment during pregnancy largely prevented negative effects of hyperglycemia, accelerated developmental milestones, and enhanced memory task performance.
- Insulin administration induced hyper-ramification of hippocampal microglia in both male and female offspring.
Conclusions:
- Maternal diabetes adversely affects offspring neurodevelopment and behavior in a sex-specific manner, with females exhibiting memory impairments.
- Insulin therapy is effective in preventing many detrimental effects of maternal hyperglycemia on offspring, but may also induce unique developmental modulations.
- The study underscores the critical need to consider sex differences when evaluating the impact of maternal diabetes and its treatment on offspring neurodevelopment.
Abstract:
Diabetes during pregnancy has been shown to affect the central nervous system (CNS) of the offspring, resulting in short- and long-term adverse effects. Children of diabetic mothers are more likely to develop cognitive impairment, also having increased susceptibility to psychiatric disorders. Microglia, the immune cells of the CNS, work as sensors of environmental changes, namely metabolic challenges, as early as the intrauterine period. During this period, microglia is actively involved in processes of neurogenesis, synaptic pruning and detection of any environmental alteration that may impact brain development. The remarkable sex dimorphism in neurodevelopment, as well as sex differences in the morphology and immune function of microglia during development, led us to clarify if maternal diabetes affects specific behavioral traits and microglia morphology during infancy in a sex-specific manner. Another important goal of this study was to clarify if insulin, the gold standard treatment of diabetes during gestation, could prevent maternal diabetes-induced behavioral changes, as well as microglia morphology, also considering sex specificities. Other molecular and cellular players potentially involved in the link between changes in metabolism and behavior were also analyzed in the hippocampus, a brain region implicated in cognition and other behavioral outcomes. Diabetes during pregnancy globally delayed female and male offspring development and was associated with impairments in recognition memory, but only in female offspring. In line with these results, at early and late infancy, some molecular and cellular markers were altered in offspring hippocampus in a sex-specific manner. The strict control of glycemia by insulin during pregnancy prevented most of the negative effects induced by uncontrolled hyperglycemia. Notably, insulin administration to diabetic dams may also modulate offspring development in a way that differs from what is observed in physiological conditions, since it promoted the expedited acquisition of developmental milestones and of discrimination ability at memory test, also inducing a hyper-ramification of male and female hippocampal microglia. Importantly, this study highlights the importance of analyzing the impact of maternal diabetes and insulin therapy, taking into account sex differences, since male and female present different vulnerabilities to hyperglycemia in this critical period of life.
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