All Relations between sv2a and \u03b1-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid

Publication Sentence Publish Date Extraction Date Species
Eric Witherspoon, Nicholas Zuczek, Gabrielle Williams, Briana Bernstein, Anjik Ghosh, Marko Culjat, Suhasini Kaushal, Patrick A Forcell. A single exposure to brivaracetam or perampanel does not cause cell death in neonatal rats. Frontiers in pediatrics. vol 12. 2024-10-01. PMID:39350791. brivaracetam (brv) and perampanel (per) are two newer generation anti-seizure medications and are of interest based on their mechanisms of action (sv2a modulator, ampa antagonist, respectively), as other drugs with these mechanisms of action do not trigger acute neurotoxicity. 2024-10-01 2024-10-03 rat
Motohiro Okada, Kouji Fukuyama, Takashi Shiroyama, Yuto Ued. Brivaracetam prevents astroglial l-glutamate release associated with hemichannel through modulation of synaptic vesicle protein. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. vol 138. 2021-07-22. PMID:33706129. to explore the antiepileptic/anticonvulsive mechanism of brivaracetam associated with sv2a modulation, this study determined concentration-dependent effects of brivaracetam on astroglial l-glutamate release associated with connexin43 (cx43), tumour-necrosis factor-α (tnfα) and α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (ampa)/glutamate receptor of rat primary cultured astrocytes using ultra-high-performance liquid chromatography. 2021-07-22 2023-08-13 rat
Ting Wu, Katsutoshi Ido, Makoto Ohgoh, Takahisa Hanad. Mode of seizure inhibition by sodium channel blockers, an SV2A ligand, and an AMPA receptor antagonist in a rat amygdala kindling model. Epilepsy research. vol 154. 2020-07-13. PMID:31035244. mode of seizure inhibition by sodium channel blockers, an sv2a ligand, and an ampa receptor antagonist in a rat amygdala kindling model. 2020-07-13 2023-08-13 rat
Michael A Rogawski, Wolfgang Löscher, Jong M Rh. Mechanisms of Action of Antiseizure Drugs and the Ketogenic Diet. Cold Spring Harbor perspectives in medicine. vol 6. issue 5. 2017-12-07. PMID:26801895. asds act by modulation of voltage-gated ion channels, including sodium, calcium, and potassium channels; by enhancement of γ-aminobutyric acid (gaba)-mediated inhibition through effects on gabaa receptors, the gaba transporter 1 (gat1) gaba uptake transporter, or gaba transaminase; through interactions with elements of the synaptic release machinery, including synaptic vesicle 2a (sv2a) and α2δ; or by blockade of ionotropic glutamate receptors, including α-amino-3-hydroxy-5-methyl-4-isoxazole-propionate (ampa) receptors. 2017-12-07 2023-08-13 Not clear
Silvia Olivera Bravo, Jeremy Henley, Daniel Rodriguez-Ithurrald. Acetylcholinesterase effects on glutamate receptors. Chemico-biological interactions. vol 157-158. 2006-02-24. PMID:16429521. a selective potentiation of ampa receptors (ampar) binding in ampar-enriched layers undergoing synaptogenesis plus an increased surface expression of synaptic clusters of glur1, glur2, and sv2a was found. 2006-02-24 2023-08-12 rat