Glutamate and Brain Glutaminases in Drug Addiction

dc.contributor.author
Márquez, Javier
dc.contributor.author
Campos-Sandoval, José A.
dc.contributor.author
Peñalver, Ana
dc.contributor.author
Matés, José M.
dc.contributor.author
Segura, Juan A.
dc.contributor.author
Blanco Calvo, Eduardo
dc.contributor.author
Alonso, Francisco J.
dc.contributor.author
Rodríguez de Fonseca, Fernando
dc.date.accessioned
2024-12-05T22:16:02Z
dc.date.available
2024-12-05T22:16:02Z
dc.date.issued
2018-04-13T14:52:29Z
dc.date.issued
2018-04-13T14:52:29Z
dc.date.issued
2017
dc.identifier
https://doi.org/10.1007/s11064-016-2137-0
dc.identifier
0364-3190
dc.identifier
1573-6903
dc.identifier
http://hdl.handle.net/10459.1/63098
dc.identifier.uri
http://hdl.handle.net/10459.1/63098
dc.description.abstract
Glutamate is the principal excitatory neurotransmitter in the central nervous system and its actions are related to the behavioral effects of psychostimulant drugs. In the last two decades, basic neuroscience research and preclinical studies with animal models are suggesting a critical role for glutamate transmission in drug reward, reinforcement, and relapse. Although most of the interest has been centered in post-synaptic glutamate receptors, the presynaptic synthesis of glutamate through brain glutaminases may also contribute to imbalances in glutamate homeostasis, a key feature of the glutamatergic hypothesis of addiction. Glutaminases are the main glutamate-producing enzymes in brain and dysregulation of their function have been associated with neurodegenerative diseases and neurological disorders; however, the possible implication of these enzymes in drug addiction remains largely unknown. This mini-review focuses on brain glutaminase isozymes and their alterations by in vivo exposure to drugs of abuse, which are discussed in the context of the glutamate homeostasis theory of addiction. Recent findings from mouse models have shown that drugs induce changes in the expression profiles of key glutamatergic transmission genes, although the molecular mechanisms that regulate drug-induced neuronal sensitization and behavioral plasticity are not clear.
dc.description.abstract
This work was financially supported by Grants RD12/0028/0013 (JM) and RD12/0028/0001 (FRF) of the RTA RETICS network from the Spanish Health Institute Carlos III, Grant SAF2015-64501-R from the Spanish Ministry of Economy and Competitivity (to JM and JMM) and Excellence Grant CVI-6656 (Regional Andalusian government) (to JM).
dc.language
eng
dc.publisher
Springer Verlag
dc.relation
info:eu-repo/grantAgreement/MINECO//SAF2015-64501-R/ES/ISOENZIMAS GLUTAMINASA EN LA TRANSFORMACION NEOPLASICA Y LA FUNCION CEREBRAL:/
dc.relation
Versió postprint del document publicat a https://doi.org/10.1007/s11064-016-2137-0
dc.relation
Neurochemical Research, 2017, vol. 42, núm. 3, p. 846-857
dc.rights
(c) Springer International Publishing AG. Part of Springer Nature, 2017
dc.rights
info:eu-repo/semantics/openAccess
dc.subject
Glutaminase
dc.subject
Cocaine
dc.subject
Drugs of abuse
dc.subject
Glutamate
dc.subject
Glutamatergic neuroadaptations
dc.title
Glutamate and Brain Glutaminases in Drug Addiction
dc.type
article
dc.type
acceptedVersion


Files in this item

FilesSizeFormatView

There are no files associated with this item.

This item appears in the following Collection(s)