Cargando…
NMDA receptor antagonists ketamine and Ro25-6981 inhibit evoked release of glutamate in vivo in the subiculum
Preclinical and clinical data have identified ketamine, a non-selective NMDAR (N-methyl-D-aspartate receptor) antagonist, as a promising medication for patients who do not respond to treatment with monoamine-based antidepressants. Moreover, unlike the current monoamine-based antidepressants, ketamin...
Autores principales: | Stan, T L, Alvarsson, A, Branzell, N, Sousa, V C, Svenningsson, P |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2014
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4080320/ https://www.ncbi.nlm.nih.gov/pubmed/24893066 http://dx.doi.org/10.1038/tp.2014.39 |
Ejemplares similares
-
Ketamine and Ro 25-6981 Reverse Behavioral Abnormalities in Rats Subjected to Dietary Zinc Restriction
por: Pochwat, Bartłomiej, et al.
Publicado: (2020) -
Structural connectivity and subcellular changes after antidepressant doses of ketamine and Ro 25-6981 in the rat: an MRI and immuno-labeling study
por: Pascual-Antón, Raquel, et al.
Publicado: (2021) -
The Neurogenesis Actuator and NR2B/NMDA Receptor Antagonist Ro25-6981 Consistently Improves Spatial Memory Retraining Via Brain Region-Specific Gene Expression
por: Gruden, Marina A., et al.
Publicado: (2018) -
The GluN2B-Selective Antagonist Ro 25-6981 Is Effective against PTZ-Induced Seizures and Safe for Further Development in Infantile Rats
por: Mareš, Pavel, et al.
Publicado: (2021) -
N-methyl D-aspartate receptor subtype 2B antagonist, Ro 25-6981, attenuates neuropathic pain by inhibiting postsynaptic density 95 expression
por: Huang, Ling-Er, et al.
Publicado: (2018)