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Excitatory actions of gaba during development: the nature of the nurture.

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TLDR
This work proposes that GABA becomes inhibitory by the delayed expression of a chloride exporter, leading to a negative shift in the reversal potential for choride ions, and provides a solution to the problem of how to excite developing neurons to promote growth and synapse formation.
Abstract
In the immature brain, GABA (gamma-aminobutyric acid) is excitatory, and GABA-releasing synapses are formed before glutamatergic contacts in a wide range of species and structures. GABA becomes inhibitory by the delayed expression of a chloride exporter, leading to a negative shift in the reversal potential for choride ions. I propose that this mechanism provides a solution to the problem of how to excite developing neurons to promote growth and synapse formation while avoiding the potentially toxic effects of a mismatch between GABA-mediated inhibition and glutamatergic excitation. As key elements of this cascade are activity dependent, the formation of inhibition adds an element of nurture to the construction of cortical networks.

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Practical approaches to adverse outcome pathway development and weight-of-evidence evaluation as illustrated by ecotoxicological case studies.

TL;DR: Four ecotoxicological AOP case studies are described, developed for different purposes, and several web-based tools that can aid in AOP assembly and evaluation of weight of evidence for scientific robustness of AOP components are highlighted.
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Acute spinal cord injury (SCI) transforms how GABA affects nociceptive sensitization.

TL;DR: Evidence is provided that spinal cord injury transforms how GABA affects nociceptive transmission within the spinal cord, recapitulating an earlier developmental state wherein GABA has an excitatory effect and the results suggest that GABAergic neurons drive, rather than inhibit, the development of nocICEptive sensitization after spinal injury.
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Population dynamics of the modified theta model: macroscopic phase reduction and bifurcation analysis link microscopic neuronal interactions to macroscopic gamma oscillation.

TL;DR: A modification of the theta model, which possesses voltage-dependent dynamics with appropriate synaptic interactions, is derived and it is found that under appropriate balance of parameters, two branches of bifurcation are found in the analysis of the FPE.
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Effect of depolarizing GABAA-mediated membrane responses on excitability of Cajal-Retzius cells in the immature rat neocortex

TL;DR: It is demonstrated that focal GABA application induces heterogeneous rheobase shifts in Cajal-Retzius cells that could not be predicted reliably from [Cl(-)](i) or the GABAergic membrane depolarization.
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Proton magnetic resonance spectroscopy of malformations of cortical development causing epilepsy.

TL;DR: Results of proton magnetic resonance spectroscopy indicate that MCD show spectroscopic features of primitive tissue and abnormal metabolism of both inhibitory and excitatory neurotransmitters.
References
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Journal ArticleDOI

The K+/Cl- co-transporter KCC2 renders GABA hyperpolarizing during neuronal maturation.

TL;DR: It is shown that, in pyramidal neurons of the rat hippocampus, the ontogenetic change in GABAA-mediated responses from depolarizing to hyperpolarizing is coupled to a developmental induction of the expression of the neuronal Cl−-extruding K+/Cl − co-transporter, KCC2 (ref. 7).
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Gamma (40-100 Hz) oscillation in the hippocampus of the behaving rat

TL;DR: It is suggested that gamma oscillation emerges from an interaction between intrinsic oscillatory properties of interneurons and the network properties of the dentate gyrus and that Gamma oscillation in the CA3-CA1 circuitry is suppressed by either the hilar region or the entorhinal cortex.
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Synaptic Assembly of the Brain in the Absence of Neurotransmitter Secretion

TL;DR: Synaptic connectivity does not depend on neurotransmitter secretion, but its maintenance does, and neurotransmitter secretion probably functions to validate already established synaptic connections.
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Giant synaptic potentials in immature rat CA3 hippocampal neurones.

TL;DR: In neurones in which evoked GDPs were blocked by bicuculline, a NMDA‐mediated component was revealed by increasing the strength or the frequency of stimulation, and during the second week of postnatal life, superfusion with bicuciulline induced, as in adult slices, interictal discharges.
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