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Journal ArticleDOI

Amygdala-kindled and pentylenetetrazole-induced seizures in glutamate transporter GLAST-deficient mice.

TLDR
Results indicate that GLAST is one of factors determining seizure susceptibility and more severe stages of PTZ-induced seizures than GLAST(+/+) mice, and the latency to the onset of seizures was significantly shorter for the mutant mice.
About
This article is published in Brain Research.The article was published on 1999-10-16. It has received 110 citations till now. The article focuses on the topics: Epileptogenesis & Epilepsy.

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Citations
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Journal ArticleDOI

Kindling and status epilepticus models of epilepsy: rewiring the brain.

TL;DR: This review focuses on the remodeling of brain circuitry associated with epilepsy, particularly in excitatory glutamate and inhibitory GABA systems, including alterations in synaptic efficacy, growth of new connections, and loss of existing connections.
Journal ArticleDOI

Mechanisms of Disease: astrocytes in neurodegenerative disease.

TL;DR: Understanding of the normative biology of astrocytes has been aided by the development of animal models in which astroCyte-specific proteins and pathways have been manipulated, and mouse models of neurodegenerative diseases have revealedAstrocyte- specific pathologies that contribute to Neurodegeneration.
Journal ArticleDOI

Glutamate as a neurotransmitter in the healthy brain.

TL;DR: The present review provides a brief historical description, gives a short overview of glutamate as a transmitter in the healthy brain, and comments on the so-called glutamate–glutamine cycle.
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The glutamate/neutral amino acid transporter family SLC1: molecular, physiological and pharmacological aspects

TL;DR: Selective inhibition of the neuronal glutamate transporter EAAC1 (SLC1A1) may be of therapeutic interest to block glutamate release from neurons during ischemia, and upregulation of the glial glutamate transporter GLT1 may help protect motor neurons in patients with amyotrophic lateral sclerosis (ALS), since loss of function ofGLT1 has been associated with the pathogenesis of certain forms of ALS.
Journal ArticleDOI

Glutamate transporters: animal models to neurologic disease.

TL;DR: Animal models of glutamate transporter dysfunction have revealed a significant role for these proteins in pathologic conditions such as neurodegenerative diseases, epilepsy, stroke, and central nervous system tumors.
References
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Journal ArticleDOI

Knockout of Glutamate Transporters Reveals a Major Role for Astroglial Transport in Excitotoxicity and Clearance of Glutamate

TL;DR: It is suggested that glial glutamate transporters provide the majority of functional glutamate transport and are essential for maintaining low extracellular glutamate and for preventing chronic glutamate neurotoxicity.
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Epilepsy and Exacerbation of Brain Injury in Mice Lacking the Glutamate Transporter GLT-1

TL;DR: Homozygous mice deficient in GLT-1, a widely distributed astrocytic glutamate transporter, show lethal spontaneous seizures and increased susceptibility to acute cortical injury, which can be attributed to elevated levels of residual glutamate in the brains of these mice.
Journal ArticleDOI

Localization of neuronal and glial glutamate transporters

TL;DR: The cellular and subcellular distributions of the glutamate transporter subtypes EAAC1, GLT-1, and GLAST in the rat CNS were demonstrated using anti-peptide antibodies that recognize the C-terminal domains of each transporter.
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Primary structure and functional characterization of a high-affinity glutamate transporter

TL;DR: A complementary DNA encoding an electrogenic Na+ but not Cl−-dependent high-affinity glutamate transporter (named EAAC1) is isolated from rabbit small intestine by expression in Xenopus oocytes and transcripts are found in specific neuronal structures in the central nervous system as well as in the small intestine, kidney, liver and heart.
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Cloning and expression of a rat brain L-glutamate transporter.

TL;DR: An antibody against a glial L-glutamate transporter from rat brain is used to isolate a complemen-tary DNA clone encoding this transporter, which predicts a protein of 573 amino acids with 8–9 putative transmembrane α-helices that seems to be a member of a new family of transport molecules.
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