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Neuroreport ; 11(10): 2293-7, 2000 Jul 14.
Artigo em Inglês | MEDLINE | ID: mdl-10923688

RESUMO

Beta-amyloid (A beta) accumulation is believed to contribute to neuronal cell death in Alzheimer's disease. To understand the role of cAMP in the regulation of A beta induced cell death, we used 8-chlorophenylthio-cAMP (8-CPT-cAMP, a cAMP analog) to raise intracellular cAMP levels. Exposure of rat cortical neurons to A beta(25-35) resulted in a gradual increase in lactate dehydrogenase (LDH) over 48 h, which was preceded by a transient elevation in caspase-3-like activity. In the presence of 8CPT-cAMP, both caspase-3 activity and LDH release was significantly reduced. These data suggest that elevation of intracellular cAMP levels attenuate A beta-induced neurotoxicity and may delay or prevent the onset of A beta-induced neurodegeneration.


Assuntos
Peptídeos beta-Amiloides/farmacologia , Morte Celular/efeitos dos fármacos , Córtex Cerebral/citologia , AMP Cíclico/análogos & derivados , AMP Cíclico/farmacologia , AMP Cíclico/fisiologia , Neurônios/efeitos dos fármacos , Fragmentos de Peptídeos/farmacologia , Tionucleotídeos/farmacologia , Animais , Caspase 3 , Caspases/metabolismo , Células Cultivadas , Córtex Cerebral/fisiologia , Embrião de Mamíferos , Neurônios/citologia , Neurônios/fisiologia , Neurotoxinas/farmacologia , Ratos , Ratos Sprague-Dawley
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