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Exposure of isoflurane-treated cells to hyperoxia decreases cell viability and activates the mitochondrial apoptotic pathway
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文摘

The effects of hyperoxia on rat PC12 cells that were exposed to isoflurane.

Isoflurane decrease cell viability in a dose- and time-dependent manner.

This effect is augmented by hyperoxia.

ROS, mitochondrial apoptotic signaling pathway, and β-amyloid may be involved.

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