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Journal of Zhejiang University. Medical sciences ; (6): 146-149, 2007.
Artículo en Chino | WPRIM | ID: wpr-271559

RESUMEN

<p><b>OBJECTIVE</b>To investigate the effects of histamine on the neurotoxicity induced by beta-amyloid(1-42)(Abeta42) in rat phaeochromocytoma (PC12) cells.</p><p><b>METHODS</b>The in vitro model of Alzheimer's disease was constructed with A beta42-treated PC12 cells. Cell morphology and MTT assay were used to evaluate the cell toxicity and histamine effects. The different histamine antagonists were applied to investigate the involvement of receptor subtypes.</p><p><b>RESULT</b>The neurotoxicity was induced by A beta42 in a concentration-dependent manner, which was reversed by histamine at concentration of 10(-7), 10(-6) mol/L. The effect was reversed by H(2) antagonist zolantidine and H(3)antagonist clobenpropit, but not by H(1) antagonist diphenhydramine.</p><p><b>CONCLUSION</b>Histamine reduces neurotoxicity induced by beta-amyloid(1-42), which may be mediated by H(2) and H(3)receptors.</p>


Asunto(s)
Animales , Ratas , Enfermedad de Alzheimer , Metabolismo , Péptidos beta-Amiloides , Toxicidad , Benzotiazoles , Farmacología , Difenhidramina , Farmacología , Relación Dosis-Respuesta a Droga , Histamina , Farmacología , Antagonistas de los Receptores H2 de la Histamina , Farmacología , Antagonistas de los Receptores Histamínicos H3 , Farmacología , Imidazoles , Farmacología , Fármacos Neuroprotectores , Metabolismo , Farmacología , Células PC12 , Fenoxipropanolaminas , Farmacología , Piperidinas , Farmacología , Receptores Histamínicos H2 , Metabolismo , Receptores Histamínicos H3 , Metabolismo , Tiourea , Farmacología
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