Thus, depletion of dietary iron stores are instantly detected via homeostatic regulatory mechanisms. These mechanisms are regulated by the blood-brain barrier in response to iron status. Mostly, the overall concentration of iron in brain tissue is adequate, with concentrations differing according to brain region and stage of development. Some areas of the brain that are important for cognition—such as the cortex, hippocampus, and striatum—are more sensitive to iron deficiency than others10. Iron affects the proper myelination of neurons and is a co-factor for a number of enzymes involved in neurotransmitter synthesis, including tryptophan hydroxylase (serotonin) and tyrosine hydroxylase (norepinephrine and dopamine)10,12. The role of iron in optimal neurotransmitter functioning is supported by a research study. The study’s results explains that the distribution of iron in the brain overlaps with the distribution of the neurotransmitters dopamine (DA) and gamma-aminobutyric acid (GABA)11. This co-localization of iron, DA, and GABA is important because the brain areas in which this occurs (e.g., the frontal cortex) regulate mental, cognitive, emotional, and behavioral functions in children young 11. However, DA is the only neurotransmitter that has been consistently related to experimental changes in iron status. Animal studies have found that iron deficiency results in a reduction of DA
Thus, depletion of dietary iron stores are instantly detected via homeostatic regulatory mechanisms. These mechanisms are regulated by the blood-brain barrier in response to iron status. Mostly, the overall concentration of iron in brain tissue is adequate, with concentrations differing according to brain region and stage of development. Some areas of the brain that are important for cognition—such as the cortex, hippocampus, and striatum—are more sensitive to iron deficiency than others10. Iron affects the proper myelination of neurons and is a co-factor for a number of enzymes involved in neurotransmitter synthesis, including tryptophan hydroxylase (serotonin) and tyrosine hydroxylase (norepinephrine and dopamine)10,12. The role of iron in optimal neurotransmitter functioning is supported by a research study. The study’s results explains that the distribution of iron in the brain overlaps with the distribution of the neurotransmitters dopamine (DA) and gamma-aminobutyric acid (GABA)11. This co-localization of iron, DA, and GABA is important because the brain areas in which this occurs (e.g., the frontal cortex) regulate mental, cognitive, emotional, and behavioral functions in children young 11. However, DA is the only neurotransmitter that has been consistently related to experimental changes in iron status. Animal studies have found that iron deficiency results in a reduction of DA