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The Use of Trace Eyeblink Classical Conditioning to Assess Hippocampal Dysfunction in a Rat Model of Fetal Alcohol Spectrum Disorders
Published on: August 5, 2017
Fetal alcohol spectrum disorders and their transmission through genetic and epigenetic mechanisms
Edward A Mead1, Dipak K Sarkar1
1Rutgers Endocrine Program, Department of Animal Sciences, Rutgers, The State University of New Jersey, New Brunswick, NJ, USA.
Insights
Fetal alcohol spectrum disorders (FASD), caused by prenatal alcohol exposure, affect approximately 1% of US children. Research highlights FASD's impact on the HPA axis, immune system, and potential transgenerational effects.
Area of Science:
- Neuroscience
- Developmental Biology
- Public Health
Background:
- Fetal alcohol spectrum disorders (FASD) result from prenatal ethanol exposure.
- FASD affects approximately 1% of US children and is a leading cause of preventable mental retardation.
- These disorders are linked to significant alterations in the hypothalamic-pituitary-adrenal (HPA) axis and immune function.
Purpose of the Study:
- To review current literature on FASD.
- To emphasize the role of HPA axis dysfunction in FASD.
- To explore the connection between HPA axis dysfunction and transgenerational inheritance in FASD.
Main Methods:
- Literature review of existing studies on FASD.
- Analysis of research focusing on HPA axis function in FASD.
- Examination of studies investigating epigenetic factors and transgenerational inheritance in FASD.
Main Results:
- Prenatal ethanol exposure leads to HPA axis dysregulation, causing lifelong impairments.
- FASD is associated with immune system deficits, increasing susceptibility to diseases like cancer.
- Emerging evidence suggests a role for genetic and epigenetic factors in FASD, including potential transgenerational effects.
Conclusions:
- FASD presents a significant public health challenge with lifelong consequences.
- HPA axis dysfunction is a critical mechanism underlying FASD's impact.
- Further research into epigenetic factors and transgenerational inheritance is crucial for understanding and preventing FASD.
Abstract:
Fetal alcohol spectrum disorders (FASD) are a group of related conditions that arise from prenatal exposure to maternal consumption of the teratogen, ethanol. It has been estimated that roughly 1% of children in the US suffer from FASD (Sampson etal., 1997), though in some world populations, such as inhabitants of some poorer regions of South Africa, the rate can climb to as high as 20% (May etal., 2013). FASD are the largest cause of mental retardation in U.S. neonates, and ironically, are entirely preventable. FASD have been linked to major changes in the hypothalamic-pituitary-adrenal (HPA) axis, resulting in lifelong impairments through mental disorders, retardation, and sensitivity to stress. FASD are linked to an impaired immune system which consequently leads to an elevated risk of cancer and other diseases. FASD arise from a complex interplay of genetic and epigenetic factors. Here, we review current literature on the topic to tease apart what is known in these areas particularly emphasizing HPA axis dysfunction and how this ties into new studies of transgenerational inheritance in FASD.
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