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  • 标题:Xenon prevents cellular damage in differentiated PC-12 cells exposed to hypoxia
  • 本地全文:下载
  • 作者:Christian Petzelt ; Per Blom ; Wolfgang Schmehl
  • 期刊名称:BMC Neuroscience
  • 印刷版ISSN:1471-2202
  • 电子版ISSN:1471-2202
  • 出版年度:2004
  • 卷号:5
  • 期号:1
  • 页码:1
  • DOI:10.1186/1471-2202-5-55
  • 语种:English
  • 出版社:BioMed Central
  • 摘要:Background The neuroprotective effect of xenon has been demonstrated for glutamatergic neurons. In the present study it is investigated if dopaminergic neurons, i.e. nerve-growth-factor differentiated PC-12 cells, are protected as well against hypoxia-induced cell damage in the presence of xenon. Results Pheochromocytoma cells differentiated by addition of nerve growth factor were placed in a N2-saturated atmosphere, a treatment that induced release of dopamine, reaching a maximum after 30 min. By determining extracellular lactate dehydrogenase concentration as marker for concomitant cellular damage, a substantial increase of enzymatic activity was found for N2-treated cells. Replacement of N2 by xenon in such a hypoxic atmosphere resulted in complete protection against cellular damage and prevention of hypoxia-induced dopamine release. Intracellular buffering of Ca2+ using the Ca-chelator 1, 2- bis (2-Aminophenoxy)ethane-N,N,N',N'-tetraacetic acid tetrakis (acetoxymethyl) ester (BAPTA) reduced the neuroprotective effect of xenon indicating the essential participation of intracellular Ca2+-ions in the process of xenon-induced neuroprotection. Conclusions The results presented demonstrate the outstanding property of xenon to protect neuron-like cells in a hypoxic situation.
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