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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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Ontogeny and reversal of brain circuit abnormalities in a preclinical model of PCOS.

TL;DR: It is determined that increased GABA input to GnRH neurons occurs prior to androgen excess and the manifestation of reproductive impairments in PNA mice, suggesting that brain circuit abnormalities precede the postpubertal development of PCOS traits.
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Developmental and maintenance defects in Rett syndrome neurons identified by a new mouse staging system in vitro

TL;DR: The results point to both a developmental and a maintenance setback affecting the final shape and function of neurons in RTT, suggesting increased synapse elimination.
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GABAergic excitation of vasopressin neurons: possible mechanism underlying sodium-dependent hypertension.

TL;DR: In this article, changes in GABAA receptor-mediated inhibition in AVP-secreting magnocellular neurons contribute to the generation of Na+-dependent hypertension.
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Nicotinic modulation of network and synaptic transmission in the immature hippocampus investigated with genetically modified mice

TL;DR: It is found that early in postnatal life α7* and β2* nAChRs exert a fine regional modulation of GABAergic and glutamatergic transmission that underlies nicotine‐elicited changes in network synchronization.
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Shift of intracellular chloride concentration in ganglion and amacrine cells of developing mouse retina.

TL;DR: The hypothesis that a shift from high [Cl-]i to low causes GABA to switch from excitatory to inhibitory is supported.
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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