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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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Age-dependent Spontaneous Hyperexcitability and Impairment of GABAergic Function in the Hippocampus of Mice Lacking trkB

TL;DR: The results indicate that the lack of TrkB signaling during development impairs GABAergic neurotransmission, thereby leading to an age-dependent decrease followed by an increase in the intrinsic excitability of neuronal circuits.
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Neurons on the move: migration and lamination of cortical interneurons.

TL;DR: The notion of additional sources of interneuron progenitors found in human and non-human primates are discussed and the disruption of early developmental events can instigate a loss in GABAergic function are illustrated.
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Sex-dependent effects of nicotine on the developing brain.

TL;DR: It is shown that gonadal hormone‐mediated sexual differentiation of the brain may be an important determinant of sex differences in the effects of nicotine, and the importance of including these factors in preclinical research that models tobacco dependence is stressed.
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Restoring GABAergic inhibition rescues memory deficits in a Huntington’s disease mouse model

TL;DR: It is demonstrated that the action of the neurotransmitter GABA has switched from inhibitory to excitatory, and by treating HD mice with a clinically used diuretic (bumetanide), which restores inhibitory GABA, rescued the learning and memory deficits.
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Intracellular chloride ions regulate the time-course of GABA-mediated inhibitory synaptic transmission

TL;DR: The decay time course of GABAergic inhibitory synaptic currents is considerably faster when recorded with physiological internal Cl− concentrations than with symmetrical Cl− solutions, due to a direct modulation of the GABAA receptor.
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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