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Ketamine exacerbates cortical neuroapoptosis under hyperoxic conditions by upregulating expression of the Nmethyl-D-aspartate receptor subunit NR1 in the developing rat brain
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Ketamine and hyperoxia are widely used in obstetric and pediatric settings. Either ketamine or hyperoxia has been reported to cause neuroapoptosis in the developing brain, and ketamine-induced neuronal apoptosis may involve a compensatory upregulation of the N-methyl-D-aspartate (NMDA) receptor NR1 subunit. T
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