右美托咪定
医学
内质网
神经保护
SH-SY5Y型
异丙酚
细胞凋亡
药理学
麻醉
未折叠蛋白反应
细胞生物学
细胞培养
镇静
生物
生物化学
神经母细胞瘤
遗传学
作者
Masayuki Somei,Manami Inagaki,Tatsunori Oguchi,Ran Ono,Mayumi Tsuji,Katsuji Oguchi
出处
期刊:The Showa University Journal of Medical Sciences
[The Showa University Society]
日期:2016-01-01
卷期号:28 (3): 219-231
被引量:2
标识
DOI:10.15369/sujms.28.219
摘要
Propofol is a short-acting intravenous anesthetic agent.Dexmedetomidine, a highly selective α 2 -adrenergic receptor agonist, has a well-known sedative effect.Both agents exhibit cytoprotective effects in the nervous system under ischemic conditions.Recently, the combination of propofol plus dexmedetomidine was used for the sedation of mechanically ventilated patients in an intensive care unit, but there are few experimental reports of the protective effects of the propofol plus dexmedetomidine combination in cells.Meanwhile, intraoperative brain ischemia-reperfusion induces endoplasmic reticulum (ER) stress-mediated apoptosis.The aim of the present study was to clarify molecular details underlying the neuroprotection afforded by the combination of propofol plus dexmedetomidine against thapsigargin (TG) -induced ER stress in human neuroblastoma SH-SY5Y cells, and whether the combination provided more ef cient neuroprotection.TG was used to generate ER stress in SH-SY5Y cells.Cells were pretreated with propofol or dexmedetomidine, individually or in combination, for 1 h before cotreatment with TG for 20 h.There was a signi cant increase in [Ca 2+ ] i , caspase activation, and the expression of ER stress biomarkers in TG-induced apoptotic cells.The increase in [Ca 2+ ] i and the induction of ER stress by TG were suppressed by pretreatment with propofol, dexmedetomidine, and their combination.The dexmedetomidineinduced reduction in caspase activity and ER stress biomarkers was inhibited by pretreatment with an α 2 -adrenergic receptor antagonist, but was enhanced by pretreatment with a cAMP inhibitor.Treatment with the propofol plus dexmedetomidine combination exhibited the strongest protection against TG-induced apoptosis.These results demonstrate that the combination of propofol plus dexmedetomidine at clinically relevant concentrations suppresses ER stress-induced apoptosis in neuroblastoma SH-SY5Y cells.The ndings suggest that the combination of propofol plus dexmedetomidine within a clinically relevant concentration range may be used safely in patients.
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