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Postnatal Overfeeding in Rodents Induces a Neurodevelopment Delay and Anxious-like Behaviour Accompanied by Sex- and
Andreia Amaro1,2,3, Diana Sousa1,2,3, Mariana Sá-Rocha1,2,3
1Coimbra Institute for Clinical and Biomedical Research (iCBR) and Institute of Physiology, Faculty of Medicine, University of Coimbra, 3000-548 Coimbra, Portugal.
Insights
Postnatal overfeeding impacts neurodevelopment and behavior, causing lasting changes in offspring. These effects vary by sex and brain region, affecting nutrient-sensing pathways like NPY and GABA.
Area of Science:
- Neuroscience
- Developmental Biology
- Endocrinology
Background:
- Early life nutrition significantly influences long-term neurodevelopment and behavior.
- Nutritional disturbances can disrupt neuronal connections and neuroendocrine pathways.
- Mechanisms linking postnatal nutrition to adult behavior remain unclear.
Purpose of the Study:
- To investigate sex-specific neurodevelopmental and behavioral outcomes of postnatal overfeeding.
- To explore underlying molecular mechanisms in the central nervous system.
- To examine the interplay between synaptic and neuroendocrine alterations.
Main Methods:
- Postnatal overfeeding induced via litter size reduction at postnatal day 3.
- Neurodevelopmental assessments in infancy.
- Behavioral testing (locomotion, anxiety, memory) in adolescence.
- Molecular analysis of hippocampus, hypothalamus, and prefrontal cortex.
Main Results:
- Females showed impaired developmental milestones; males had transient locomotor delays.
- Adolescent offspring exhibited anxious behavior but normal short-term memory.
- Region-specific changes in NPY1R, GABA(A), vGLUT1, and PSD95 levels were observed.
- Sex and brain region specificity in molecular alterations was evident.
Conclusions:
- Postnatal overfeeding induces sex-specific neurodevelopmental deficits and behavioral changes.
- Altered NPY and GABA signaling in specific brain regions contribute to these effects.
- Findings highlight the critical role of early nutrition in shaping brain function and behavior.
Abstract:
Nutritional disturbances during the early postnatal period can have long-lasting effects on neurodevelopment and may be related to behavioural changes at adulthood. While such neuronal connection disruption can contribute to social and behaviour alterations, the dysregulation of the neuroendocrine pathways involved in nutrient-sensing balance may also cause such impairments, although the underlying mechanisms are still unclear. We aimed to evaluate sex-specific neurodevelopmental and behavioural changes upon postnatal overfeeding and determine the potential underpinning mechanisms at the central nervous system level, with a focus on the interconnection between synaptic and neuroendocrine molecular alterations. At postnatal day 3 (PND3) litters were culled to three animals (small litter procedure). Neurodevelopmental tests were conducted at infancy, whereas behavioural tests to assess locomotion, anxiety, and memory were performed at adolescence, together with molecular analysis of the hippocampus, hypothalamus, and prefrontal cortex. At infancy, females presented impaired acquisition of an auditory response, eye opening, olfactory discrimination, and vestibular system development, suggesting that female offspring neurodevelopment/maturation was deeply affected. Male offspring presented a transitory delay in locomotor performance., while both offspring had lower upper limb strength. At adolescence, both sexes presented anxious-like behaviour without alterations in short-term memory retention. Both males and females presented lower NPY1R levels in a region-specific manner. Furthermore, both sexes presented synaptic changes in the hippocampus (lower GABAA in females and higher GABAA levels in males), while, in the prefrontal cortex, similar higher GABAA receptor levels were observed. At the hypothalamus, females presented synaptic changes, namely higher vGLUT1 and PSD95 levels. Thus, we demonstrate that postnatal overfeeding modulates offspring behaviour and dysregulates nutrient-sensing mechanisms such as NPY and GABA in a sex- and brain-region-specific manner.
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