نتایج جستجو برای: delayed neuronal death

تعداد نتایج: 476733  

Journal: :Cell death and differentiation 2007
N Plesnila L von Baumgarten M Retiounskaia D Engel A Ardeshiri R Zimmermann F Hoffmann S Landshamer E Wagner C Culmsee

Acute and chronic neurodegeneration, for example, following brain injury or Alzheimer's disease, is characterized by programmed death of neuronal cells. The present study addresses the role and interaction of p53- and NF-kappaB-dependent mechanisms in delayed neurodegeneration following traumatic brain injury (TBI). After experimental TBI in mice p53 rapidly accumulated in the injured brain tis...

Journal: :European journal of pharmacology 2002
Eduardo Candelario-Jalil Dalia Alvarez Armando González-Falcón Michel García-Cabrera Gregorio Martínez-Sánchez Nelson Merino Attilia Giuliani Olga Sonia León

Cyclooxygenase-2 is involved in the inflammatory component of the ischemic cascade, playing an important role in the delayed progression of the brain damage. The present study evaluated the pharmacological effects of the selective cyclooxygenase-2 inhibitor nimesulide on delayed neuronal death of hippocampal CA1 neurons following transient global cerebral ischemia in gerbils. Administration of ...

Journal: :Progress in neurobiology 2000
K J Banasiak Y Xia G G Haddad

In vivo models of cerebral hypoxia-ischemia have shown that neuronal death may occur via necrosis or apoptosis. Necrosis is, in general, a rapidly occurring form of cell death that has been attributed, in part, to alterations in ionic homeostasis. In contrast, apoptosis is a delayed form of cell death that occurs as the result of activation of a genetic program. In the past decade, we have lear...

Journal: :Stroke 1998
A Shiino M Matsuda J Handa B Chance

BACKGROUND AND PURPOSE Several investigations have detected evidence of apoptosis in delayed neuronal death, but controversy prevails regarding this point. Recent studies have implicated mitochondria in apoptotic events. To explore relationships between delayed neuronal death and dysfunction of the respiratory chain, we analyzed mitochondrial redox changes in the gerbil hippocampus. METHODS W...

Journal: :The Journal of neuroscience : the official journal of the Society for Neuroscience 1995
J M Dubinsky B S Kristal M Elizondo-Fournier

In vitro models of hypoxic/hypoglycemic injury reveal common mechanisms with glutamate excitotoxicity, but glutamate-induced toxicity in the absence of oxygen has never been directly addressed. Therefore, we assessed neuronal survival and intracellular calcium concentrations ([Ca2+]i) in neonatal hippocampal cultures in response to glutamate in the presence and absence of oxygen. Twenty-four ho...

Journal: :Archives of environmental health 2003
Mohamed B Abou-Donia

Organophosphorus compounds are potent neurotoxic chemicals that are widely used in medicine, industry, and agriculture. The neurotoxicity of these chemicals has been documented in accidental human poisoning, epidemiological studies, and animal models. Organophosphorus compounds have 3 distinct neurotoxic actions. The primary action is the irreversible inhibition of acetylcholinesterase, resulti...

Journal: :The Journal of biological chemistry 2005
Takuma Uo Yoshito Kinoshita Richard S Morrison

Bak is generally recognized as a multidomain, pro-apoptotic member of the Bcl-2 family. Bak and Bax are functionally redundant in non-neuronal cells and represent a mitochondrial convergence point for cell death signaling pathways. This functional redundancy, however, may not exist in neurons in which the single deletion of Bax is sufficient to confer protection against a variety of cytotoxic i...

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