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Molecular Mechanisms of Maternal Effects on Infant Neurodevelopment

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Neurobiology".

Deadline for manuscript submissions: 30 April 2026 | Viewed by 1158

Special Issue Editor


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Guest Editor
Fetal Programming and Hydroelectrolyte Metabolism Laboratory, Department of Internal Medicine, FCM, Campinas State University (UNICAMP), Campinas, Brazil
Interests: matenal effefct; nuerodevelopment; nutrient effect; brain sceince

Special Issue Information

Dear Colleagues,

The concept of 'fetal programming' suggests that an individual's phenotype can be influenced during intrauterine and perinatal development. Exposure to stressful stimuli during these critical periods may elevate the risk of metabolic, cardiovascular, and neuropsychiatric disorders later in life. Adverse stimuli often lead to increased fetal exposure to maternal glucocorticoids, which can accelerate the maturation of fetal tissues and organs, resulting in lower birth weights and a heightened risk of learning and behavioral issues. Research indicates that low placental levels of type-2 11β-hydroxysteroid dehydrogenase in stressed mothers contribute significantly to elevated fetal steroid exposure. Additionally, maternal nutritional restriction is correlated with a hyperanxious phenotype and reduced dendritic arborization in offspring neurons. However, the effects of severe gestational stressors on cellular structure and neurochemical composition in the central nervous system remain underexplored. The activation of mineralocorticoid (MR) and glucocorticoid (GR) receptors in corticotropin-releasing factor neurons enhances anxiety-like behaviors. Research also shows that type 1 CRF receptors influence neurotransmitter systems, including serotonin and dopamine, and interact with brain-derived neurotrophic factors, which play a critical role in fear and anxiety responses. This Special Issue aims to highlight research on the early effects of gestational stress on molecular and neurochemical composition, as well as cellular profiles in various brain regions of offspring, associated with the onset of stress-induced neurobehavioral changes.

Prof. Dr. José Antonio Rocha Gontijo
Guest Editor

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Keywords

  • maternal–fetal interactions
  • epigenetic regulation
  • neurodevelopmental programming
  • placental signaling
  • glucocorticoid receptors
  • brain-derived neurotrophic factor (BDNF)
  • oxidative stress
  • synaptic plasticity
  • perinatal stress
  • corticotropin-releasing factor (CRF) pathway

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Published Papers (1 paper)

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Research

18 pages, 2340 KB  
Article
Effect of the Gestational Fluoxetine Administration on Behavioral Tests and Hippocampal Structure in Male Offspring of Rats
by Marcelo Gustavo Lopes, Gabriel Boer Grigoletti-Lima, Patrícia Aline Boer and José Antonio Rocha Gontijo
Int. J. Mol. Sci. 2025, 26(21), 10758; https://doi.org/10.3390/ijms262110758 - 5 Nov 2025
Viewed by 936
Abstract
Depression is a common mental disorder during gestation, posing potential risks to fetal development and leading to behavioral and psychiatric alterations in offspring. Pharmacological intervention, particularly with selective serotonin reuptake inhibitors (SSRIs), is often necessary. This study investigated the effects of fluoxetine (F) [...] Read more.
Depression is a common mental disorder during gestation, posing potential risks to fetal development and leading to behavioral and psychiatric alterations in offspring. Pharmacological intervention, particularly with selective serotonin reuptake inhibitors (SSRIs), is often necessary. This study investigated the effects of fluoxetine (F) on behavioral and memory changes in rodent offspring following maternal gestational and lactation treatment, as well as potential alterations in hippocampal cellularity compared to control (C) progeny. Methodologies included the Morris water maze, elevated plus maze, activity monitoring, parental behavior assessments, and isotropic fractionation for the quantification of hippocampal cells and neurons. Results indicated that maternal fluoxetine exposure significantly affected the body mass, brain weight, and hippocampal metrics of the offspring, aligning with the ‘selfish brain’ hypothesis. Notably, dams treated with fluoxetine showed reduced parental care, leading to offspring with increased activity levels but no changes in anxiety-like behaviors. However, while there was a decline in learning and memory retention, as assessed by the Morris water maze, working and reference memory did not differ significantly from those of controls. This study establishes an association between fluoxetine treatment, increased hippocampal neuron density, and behavioral changes related to memory and hyperactivity, with implications for understanding behavioral disorders and informing future therapeutic interventions. Full article
(This article belongs to the Special Issue Molecular Mechanisms of Maternal Effects on Infant Neurodevelopment)
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