Abstract
GABA is the major inhibitory neurotransmitter that counterbalances excitation in the mature brain. The inhibitory action of GABA relies on the inflow of chloride ions (Cl−), which hyperpolarizes the neuron. In early development, GABA signaling induces outward Cl− currents and is depolarizing. The postnatal shift from depolarizing to hyperpolarizing GABA is a pivotal event in brain development and its timing affects brain function throughout life. Altered timing of the postnatal GABA shift is associated with several neurodevelopmental disorders. Here, we argue that the postnatal shift from depolarizing to hyperpolarizing GABA represents the final shift in a sequence of GABA shifts, regulating proliferation, migration, differentiation, and finally plasticity of developing neurons. Each developmental GABA shift ensures that the instructive role of GABA matches the circumstances of the developing network. Sensory input may be a crucial factor in determining proper timing of the postnatal GABA shift. A developmental perspective is necessary to interpret the full consequences of a mismatch between connectivity, activity and GABA signaling during brain development.
Original language | English |
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Pages (from-to) | 179-192 |
Number of pages | 14 |
Journal | Neuroscience and Biobehavioral Reviews |
Volume | 124 |
DOIs | |
Publication status | Published - May 2021 |
Bibliographical note
Funding Information:This research was supported by a TOP grant 9126021 from ZonMw . The authors thank Christian Lohmann, Martien Kas and Lotte Herstel for critically reading the manuscript.
Publisher Copyright:
© 2021 The Author(s)
Funding
This research was supported by a TOP grant 9126021 from ZonMw . The authors thank Christian Lohmann, Martien Kas and Lotte Herstel for critically reading the manuscript.
Keywords
- Autism
- Brain development
- Chloride
- Chloride cotransporters
- Circuit formation
- GABA
- GABA polarity
- KCC2
- Molecular mechanisms
- Neurodevelopmental disorders
- NKCC1