Hypoxic enhancement of evoked noradrenaline release from the human neuroblastoma SH-SY5Y

被引:7
作者
Webster, NJ [1 ]
Vaughan, PFT [1 ]
Peers, C [1 ]
机构
[1] Univ Leeds, Inst Cardiovasc Res, Leeds LS2 9JT, W Yorkshire, England
来源
MOLECULAR BRAIN RESEARCH | 2001年 / 89卷 / 1-2期
基金
英国医学研究理事会;
关键词
hypoxia; catecholamine; depolarization; muscarinic; Ca2+; exocytosis;
D O I
10.1016/S0169-328X(01)00061-4
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The effects of chronic hypoxia (2.5% O-2, 24 h) on [H-3]noradrenaline ([H-3]NA) release evoked from human neuroblastoma SH-SY5Y cells by depolarisation and by activation of muscarinic receptors was investigated. Depolarization of cells with 100 mM K+ evoked [H-3]NA release, and chronic hypoxia enhanced this release significantly. in fluorimetric studies, the Kt-evoked rises of [Ca2+](i) observed in response to 100 mM K+ were also significantly enhanced. Muscarine-evoked [H-3]NA release was also dramatically enhanced by chronic hypoxia. However. muscarine-induced release of Ca2+ from intracellular stores and subsequent capacitative Ca2+ entry was unaffected. The protein kinase C inhibitors GF 109 203X and RO-31-8220 did not prevent the enhancement of muscarine-evoked release caused by chronic hypoxia. These findings indicate that chronic hypoxia increases release of [H-3]NA from human neuroblastoma SH-SY5Y cells. Enhancement of K+-evoked release was attributable to an enhancement of depolarisation-mediated Ca2+ influx. In contrast, the larger enhancement of muscarine-evoked [H-3]NA release was not due to greater release of Ca2+ from internal stores, nor due from internal stores, nor due of sympathetic output. Furthermore, it is not attributable to activation of protein kinase C. These findings suggest that enhancement of sympathetis output, known to occur following prolonged hypoxia, may be mediated in part by enhancement of exocytosis. Elsevier Science B.V. All rights reserved.
引用
收藏
页码:50 / 57
页数:8
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