Publications by authors named "Roisin Moloney"

Article Synopsis
  • High levels of the neurosteroid allopregnanolone during pregnancy are crucial for fetal brain development, but maternal stress can lower these levels, leading to myelination issues and increased behavioral disorders in childhood.
  • Supplementing neurosteroid action with allopregnanolone analogues or using mitochondrial translocator protein (TSPO) ligands can help reverse developmental deficits that arise from low allopregnanolone levels.
  • Preterm birth significantly decreases neurosteroid support, causing severe myelination deficits; however, postnatal treatments like ganaxolone can enhance myelination and reduce hyperactivity, suggesting potential therapeutic benefits of allopregnanolone after pregnancy issues.
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The postnatal environment is challenging for the preterm neonate with exposure to hypoxic and excitotoxic events, amplified by premature loss of placentally derived neurosteroids. Between preterm birth and term equivalent age (TEA), cerebellar development continues despite these challenges. We hypothesize that neurosteroid replacement therapy during this time will support optimal cerebellar development.

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Article Synopsis
  • Preterm birth can lead to brain injuries and long-term behavioral issues due to the loss of neurosteroid support from the placenta, increasing the risk of excitotoxic damage.
  • The study used guinea pigs to test zuranolone, an analogue of allopregnanolone, by administering it to preterm pups and analyzing behavior and brain structure.
  • Zuranolone treatment improved behavioral outcomes, prevented hyperactivity in male pups, and restored myelination and neurotransmitter pathways in preterm offspring, suggesting its potential as a neuroprotective therapy for preventing long-term impairments after preterm birth.
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Article Synopsis
  • - Preterm birth can lead to serious brain injuries and developmental disorders in newborns, and current treatments are ineffective in preventing these issues.
  • - The study explores neurosteroid replacement therapy as a potential new treatment by using guinea pig brain cell cultures to understand how it might mitigate neurological damage related to preterm birth.
  • - Results show that neurosteroids such as etifoxine and zuranolone can significantly reduce cell damage and improve marker expression following oxygen-glucose deprivation, indicating their neuroprotective effects might be due to reducing glutamate levels and enhancing brain-derived neurotrophic factor (BDNF).
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Children born preterm have an increased likelihood of developing neurobehavioral disorders such as attention-deficit hyperactivity disorder (ADHD) and anxiety. These disorders have a sex bias, with males having a higher incidence of ADHD, whereas anxiety disorder tends to be more prevalent in females. Both disorders are underpinned by imbalances to key neurotransmitter systems, with dopamine and noradrenaline in particular having major roles in attention regulation and stress modulation.

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Preterm birth is known to cause impaired cerebellar development, and this is associated with the development of neurobehavioral disorders. This review aims to identify the mechanisms through which preterm birth impairs cerebellar development and consequently, increases the risk of developing neurobehavioral disorders. The severity of these disorders is directly related to the degree of prematurity, but it is also evident that even late preterm births are at significantly increased risk of developing serious neurobehavioral disorders.

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Primary cell culture is a technique that is widely used in neuroscience research to investigate mechanisms that underlie pathologies at a cellular level. Typically, mouse or rat tissue is used for this process; however, altricial rodent species have markedly different neurodevelopmental trajectories comparatively to humans. The use of guinea pig brain tissue presents a novel aspect to this routinely used cell culture method whilst also allowing for dual isolation of two major cell types from a physiologically relevant animal model for studying perinatal neurodevelopment.

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Disruptions to neurodevelopment are known to be linked to behavioral disorders in childhood and into adulthood. The fetal brain is extremely vulnerable to stimuli that alter inhibitory GABAergic pathways and critical myelination processes, programing long-term neurobehavioral disruption. The maturation of the GABAergic system into the major inhibitory pathway in the brain and the development of oligodendrocytes into mature cells capable of producing myelin are integral components of optimal neurodevelopment.

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Background: Many Polio survivors have reduced mobility, pain and fatigue, which make access to conventional forms of aerobic exercise difficult. Inactivity leads to increased risk of health problems, many of which are prevalent among Polio survivors. Aerobic exercise programmes in Polio survivors should utilise stable muscle groups and should be designed to minimise exacerbation of pain and fatigue.

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Background: Unilateral peripheral vestibular loss results in gait and balance impairment, dizziness and oscillopsia. Vestibular rehabilitation benefits patients but optimal treatment remains unknown. Virtual reality is an emerging tool in rehabilitation and provides opportunities to improve both outcomes and patient satisfaction with treatment.

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