Abstract
Reduced serotonin transporter (5-HTT) expression is associated with abnormal affective and anxiety-like symptoms in humans and rodents, but the mechanism of this effect is unknown. Transient inhibition of 5-HTT during early development with fluoxetine, a commonly used serotonin selective reuptake inhibitor, produced abnormal emotional behaviors in adult mice. This effect mimicked the behavioral phenotype of mice genetically deficient in 5-HTT expression. These findings indicate a critical role of serotonin in the maturation of brain systems that modulate emotional function in the adult and suggest a developmental mechanism to explain how low-expressing 5-HTT promoter alleles increase vulnerability to psychiatric disorders.
MeSH terms
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Animals
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Animals, Newborn
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Anxiety* / chemically induced
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Avoidance Learning / drug effects
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Behavior, Animal / drug effects
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Brain / drug effects
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Brain / growth & development
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Central Nervous System / drug effects
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Central Nervous System / growth & development
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Emotions* / drug effects
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Feeding Behavior / drug effects
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Fluoxetine / adverse effects
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Fluoxetine / toxicity*
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Humans
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Membrane Glycoproteins / antagonists & inhibitors
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Membrane Glycoproteins / genetics
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Membrane Glycoproteins / physiology*
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Membrane Transport Modulators
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Membrane Transport Proteins / antagonists & inhibitors
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Membrane Transport Proteins / genetics
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Membrane Transport Proteins / physiology*
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Mice
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Motor Activity / drug effects
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Nerve Tissue Proteins / antagonists & inhibitors
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Nerve Tissue Proteins / genetics
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Nerve Tissue Proteins / physiology*
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Polymorphism, Genetic
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Random Allocation
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Selective Serotonin Reuptake Inhibitors / adverse effects
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Selective Serotonin Reuptake Inhibitors / toxicity*
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Serotonin Plasma Membrane Transport Proteins
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Stress, Physiological
Substances
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Membrane Glycoproteins
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Membrane Transport Modulators
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Membrane Transport Proteins
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Nerve Tissue Proteins
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SLC6A4 protein, human
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Serotonin Plasma Membrane Transport Proteins
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Serotonin Uptake Inhibitors
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Slc6a4 protein, mouse
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Fluoxetine