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Related Concept Videos

Teratogenicity01:07

Teratogenicity

The ability of a drug to produce structural deformations and functional abnormalities in the developing embryo or the fetus is called teratogenicity, and the drug producing this effect is known as a teratogen. Teratogenic effects include stillbirth, miscarriage, intrauterine growth restriction, and neurocognitive delay. A teratogen may affect the embryo at different stages of development, which is important in determining the type and extent of the damage. During blastocyst formation, the early...
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Drugs affecting neurotransmitter synthesis can impact the adrenergic neuron and the synthesis of neurotransmitters. For example, α-methyltyrosine and carbidopa target specific enzymes involved in catecholamine synthesis. α-methyltyrosine inhibits the enzyme tyrosine hydroxylase, which converts tyrosine into dopamine. By blocking this enzyme, α-methyltyrosine reduces dopamine production and other catecholamines. Carbidopa, on the other hand, inhibits the enzyme dopa decarboxylase, which converts...

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Hypoxia Alters miRNAs Levels Involved in Non-Mendelian Inheritance of Autism Spectrum Disorder in Mice
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Fetal asphyxia leads to a decrease in dorsal raphe serotonergic neurons.

Eveline Strackx1, Daniël L A van den Hove, Hellen P Steinbusch

  • 1School of Mental Health and Neuroscience, Faculty of Health, Medicine and Life Sciences, Maastricht University, Maastricht, The Netherlands.

Developmental Neuroscience
|September 12, 2008
PubMed
Summary
This summary is machine-generated.

Fetal asphyxia in rats leads to increased anxiety and reduced serotonin neuron density in adulthood. These developmental insults may predispose individuals to lifelong anxiety and brain changes.

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Published on: August 5, 2017

Area of Science:

  • Neuroscience
  • Developmental Biology
  • Behavioral Science

Background:

  • Fetal asphyxia (FA) is a critical event during birth that can impact brain development.
  • Serotonergic (5-hydroxytryptamine/serotonin, 5-HT) neurons in the dorsal raphe nucleus (DRN) play a crucial role in mood regulation.
  • Age-related changes in neuronal populations are common, but the impact of early-life insults on these changes is less understood.

Purpose of the Study:

  • To investigate the long-term effects of fetal asphyxia on anxiety behaviors.
  • To examine the impact of FA on the number, density, and volume of serotonergic neurons in the DRN.
  • To determine if FA exacerbates age-related changes in the serotonergic system.

Main Methods:

  • Fetal asphyxia was induced in rats at embryonic day 17.
  • Anxiety-related behaviors were assessed using the open field test.
  • Design-based stereology was employed to quantify 5-HT neurons in the DRN at 6 and 19 months of age.

Main Results:

  • Rats exposed to FA exhibited increased anxiety behaviors at 19 months of age compared to controls.
  • No significant differences in DRN 5-HT neuron numbers were observed at 6 months.
  • At 19 months, FA rats showed significantly reduced 5-HT neuron density and volume in the DRN.
  • An age-related decline in 5-HT neuron number, density, and volume was observed within the FA group.

Conclusions:

  • Fetal asphyxia is associated with heightened anxiety and alterations in the serotonergic system in aged rats.
  • These findings suggest that early-life asphyxia may predispose individuals to serotonergic dysfunction and anxiety disorders later in life.
  • Developmental insults during critical periods can have lasting consequences on brain development and behavior.