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Cell Biol Int. 2015 Feb;39(2):164-8. doi: 10.1002/cbin.10349.

Role of miR-34c in ketamine-induced neurotoxicity in neonatal mice hippocampus.

Author information

1
Department of Anesthesiology, The First Affiliated Hospital of XinXiang Medical College, WeiHui, HeNan Province, 453100, China.

Abstract

Ketamine is a commonly used pediatric anesthetic, but it might affect development, or even induce neurotoxicity in the neonatal brain. We have used an in vivo neonatal mouse model to induce ketamine-related neurotoxicity in the hippocampus, and found that miR-34c, a microRNA associated with pathogenesis of Alzheimer's disease, was significantly upregulated during ketamine-induced hippocampal neurodegeneration. Functional assay of silencing miR-34c demonstrated that downregulation of miR-34c activated PKC-ERK pathway, upregulated anti-apoptotic protein BCL2, and ameliorated ketamine-induced apoptosis in the hippocampus. Cognitive examination with the Morris water maze test showed that ketamine-induced memory impairment was significantly improved by miR-34c downregulation. Thus, miR-34c is important in regulating ketamine-induced neurotoxicity in hippocampus.

KEYWORDS:

hippocampus; ketamine; miR-34c; neurotoxicity

PMID:
25052764
DOI:
10.1002/cbin.10349
[Indexed for MEDLINE]

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