نتایج جستجو برای: excitotoxic neuronal damage

تعداد نتایج: 339314  

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2012
João R Gomes João T Costa Carlos V Melo Federico Felizzi Patrícia Monteiro Maria J Pinto Ana R Inácio Tadeusz Wieloch Ramiro D Almeida Mário Grãos Carlos B Duarte

Brain-derived neurotrophic factor (BDNF) plays an important role in neuronal survival through activation of TrkB receptors. The trkB gene encodes a full-length receptor tyrosine kinase (TrkB.FL) and its truncated (T1/T2) isoforms. We investigated the changes in TrkB protein levels and signaling activity under excitotoxic conditions, which are characteristic of brain ischemia, traumatic brain in...

Journal: :Neuroscience research 2006
Yasuhiro Hama Hiroshi Katsuki Yoshinaga Tochikawa Chihiro Suminaka Toshiaki Kume Akinori Akaike

N-Methyl-d-aspartate (NMDA) receptors, which play an important role in neuronal excitotoxicity, require not only agonists at the glutamate-binding site but also co-agonists at the glycine site for their activation. Here we examined the role of endogenous agonists at the glycine site of NMDA receptors in excitotoxic retinal damage in vivo. To quantify the number of surviving retinal ganglion cel...

Journal: :Functional neurology 2001
D Centonze E Saulle G Bernardi P Calabresi

On the basis of a large body of experimental data showing that pharmacological modulation of glutamate receptors has a great impact on ischemia-induced neuronal death, excessive activation of glutamate receptors is widely accepted as one of the most important determinants in the development of tissue damage produced by cerebral ischemia (1). In spite of this evidence, howe v e r, how energy dep...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 2012
Beatrice D'Orsi Helena Bonner Liam P Tuffy Heiko Düssmann Ina Woods Michael J Courtney Manus W Ward Jochen H M Prehn

Excitotoxicity resulting from excessive Ca(2+) influx through glutamate receptors contributes to neuronal injury after stroke, trauma, and seizures. Increased cytosolic Ca(2+) levels activate a family of calcium-dependent proteases with papain-like activity, the calpains. Here we investigated the role of calpain activation during NMDA-induced excitotoxic injury in embryonic (E16-E18) murine cor...

2013
David C. Henshall Tobias Engel

Neuronal cell death is a pathophysiological consequence of many brain insults that trigger epilepsy and has been implicated as a causal factor in epileptogenesis. Seizure-induced neuronal death features excitotoxic necrosis and apoptosis-associated signaling pathways, including activation of multiple members of the Bcl-2 gene family. The availability of mice in which individual Bcl-2 family mem...

Journal: :Biological & pharmaceutical bulletin 2014
Taiyo Kuroki Asami Mori Tsutomu Nakahara Kenji Sakamoto Kunio Ishii

In the present study, we histologically examined the effects of nilvadipine on neuronal injury induced by intravitreal (i.v.) N-methyl-D-aspartate (NMDA) (200 nmol/eye) and intravitreal NOC12 (400 nmol/eye), a nitric oxide donor, in the rat retina. Morphometric evaluation at 7 d after injection of NMDA or NOC12 showed that treatment with nilvadipine (1 mg/kg, i.v.) 15 min prior to injection of ...

2008
J. Takanashi H. Tada H. Terada A. J. Barkovich

J. Takanashi H. Tada H. Terada A.J. Barkovich SUMMARY: Acute encephalopathy with biphasic seizures and late reduced diffusion (AESD) is a recently described clinicoradiologic syndrome. MR spectroscopy in 3 patients with AESD revealed decreased N-acetylaspartate (NAA) and elevated glutamine/glutamate complex (Glx) during the week of presentation. Afterward, Glx normalized, whereas NAA remained l...

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