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Propofol reduces synaptic strength by inhibiting sodium and calcium channels at nerve terminals 被引量:2

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摘要 Propofol (2,6-diisopropylphenol) has been widely used in clinical surgery because of its fast induction and rapid recovery effects (Miller et al., 2014). Although the underlying mechanisms are still controversial, many studies have focused on the augmentation of GABA-induced inhibition and/or modulation of glycine receptor channel activity. However, inhibition of glutamatergic synaptic transmission may also contribute to general anesthesia. The effects of general anesthetics are significantly enhanced when glutamate receptor antagonists are co-administered (Ishizaki et al., 1996).
出处 《Protein & Cell》 SCIE CAS CSCD 2019年第9期688-693,共6页 蛋白质与细胞(英文版)
分类号 Q [生物学]
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