Experimental autoimmune encephalomyelitis (EAE) is a model that mimics many of the clinical and pathological features of multiple sclerosis. We have previously found a significant reduction in the GABAergic regulation of glutamate release from synaptosomes of EAE rats during the acute stage of the disease. In order to deepen into the possible metabolic pathways responsible for this alteration, in this work we evaluate the direct effect of different GABAergic agonists on the glutamate release and synapsin I phosphorylation in synaptosomes from the frontal cortex of control and EAE animals. The results show that all tested GABA agonists negatively modulate control synaptosomes, downregulating glutamate release and synapsin I phosphorylation o...
Experimental autoimmune encephalomyelitis (EAE) is a widely used animal model for the human disease ...
The numerous γ-aminobutyric acid type A receptor (GABAAR) subtypes are differentially expressed and ...
Excitotoxic levels of released glutamate trigger a cascade of deleterious cellular events leading to...
Experimental autoimmune encephalomyelitis (EAE) is an inflammatory demyelinating disease that mimics...
We previously found that the glutamate release was decreased in synaptosomes from rat cerebral corte...
Experimental autoimmune encephalomyelitis (EAE) is an animal model that mimics many of the clinical ...
Synaptic dysfunction triggers neuronal damage in experimental autoimmune encephalomyelitis (EAE), a ...
The immunomodulador glatiramer acetate (GA) has been shown to significantly reduce the severity of s...
The astrocytic enzyme glutamine synthetase (GS) is a key regulator of glutamate and γ-aminobutyric a...
Plasticity at mammalian central synapses is thought to be essential for a variety of adaptations occ...
BACKGROUND AND PURPOSE: Glutamate transmission is dysregulated in both multiple sclerosis (MS) and e...
The aim of our investigation was to characterize the role of group I mGluRs and NMDA receptors in pa...
Cognitive impairment (CI), a debilitating and pervasive feature of multiple sclerosis (MS), is corre...
Rat cerebral cortex synaptosomes prelabeled with [3H]gamma-aminobutyric acid [( 3H]GABA) were expose...
Glutamate-mediated excitotoxicity is supposed to induce neurodegeneration in multiple sclerosis (MS)...
Experimental autoimmune encephalomyelitis (EAE) is a widely used animal model for the human disease ...
The numerous γ-aminobutyric acid type A receptor (GABAAR) subtypes are differentially expressed and ...
Excitotoxic levels of released glutamate trigger a cascade of deleterious cellular events leading to...
Experimental autoimmune encephalomyelitis (EAE) is an inflammatory demyelinating disease that mimics...
We previously found that the glutamate release was decreased in synaptosomes from rat cerebral corte...
Experimental autoimmune encephalomyelitis (EAE) is an animal model that mimics many of the clinical ...
Synaptic dysfunction triggers neuronal damage in experimental autoimmune encephalomyelitis (EAE), a ...
The immunomodulador glatiramer acetate (GA) has been shown to significantly reduce the severity of s...
The astrocytic enzyme glutamine synthetase (GS) is a key regulator of glutamate and γ-aminobutyric a...
Plasticity at mammalian central synapses is thought to be essential for a variety of adaptations occ...
BACKGROUND AND PURPOSE: Glutamate transmission is dysregulated in both multiple sclerosis (MS) and e...
The aim of our investigation was to characterize the role of group I mGluRs and NMDA receptors in pa...
Cognitive impairment (CI), a debilitating and pervasive feature of multiple sclerosis (MS), is corre...
Rat cerebral cortex synaptosomes prelabeled with [3H]gamma-aminobutyric acid [( 3H]GABA) were expose...
Glutamate-mediated excitotoxicity is supposed to induce neurodegeneration in multiple sclerosis (MS)...
Experimental autoimmune encephalomyelitis (EAE) is a widely used animal model for the human disease ...
The numerous γ-aminobutyric acid type A receptor (GABAAR) subtypes are differentially expressed and ...
Excitotoxic levels of released glutamate trigger a cascade of deleterious cellular events leading to...