IN VIVO AND IN VITRO KETAMINE EXPOSURE EXHIBITS A DOSE-DEPENDENT INDUCTION OF ACTIVITY-DEPENDENT NEUROPROTECTIVE PROTEIN IN RAT NEURONS

被引:22
作者
Brown, B. P. [1 ,4 ]
Kang, S. C. [1 ]
Gawelek, K. [1 ,2 ,4 ]
Zacharias, R. A. [1 ,3 ]
Anderson, S. R. [1 ,3 ,5 ]
Turner, C. P. [1 ]
Morris, J. K. [1 ,2 ]
机构
[1] Baldwin Wallace Univ, Neurosci Program, Berea, OH 44017 USA
[2] Baldwin Wallace Univ, Dept Biol, Berea, OH 44017 USA
[3] Baldwin Wallace Univ, Dept Psychol, Berea, OH 44017 USA
[4] Baldwin Wallace Univ, Dept Chem, Berea, OH 44017 USA
[5] Baldwin Wallace Univ, Dept Math, Berea, OH 44017 USA
关键词
activity dependent protective protein; ketamine; cortical neurons; growth cones; D-ASPARTATE RECEPTOR; ACTIN-FILAMENTS; GROWTH CONE; DEVELOPMENTAL NEUROTOXICITY; ANESTHETIC NEUROTOXICITY; NEURITE OUTGROWTH; INFLAMMATORY PAIN; FOREBRAIN CULTURE; NAP PROTECTS; CELL-DEATH;
D O I
10.1016/j.neuroscience.2014.12.076
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Anesthetic doses of ketamine induce apoptosis, as well as gene expression of activity-dependent neuroprotective protein (ADNP), a putative homeodomain transcription factor in rat pups (P7). This study investigated if ketamine induced ADNP protein in a dose-dependent manner in vitro and in vivo using primary cultures of cortical neurons and neonatal pups (P7). In vivo immunohistochemistry demonstrated a sub-anesthetic dose of ketamine increased ADNP in the somatosensory cortex (SCC) which was previously identified to be damaged by repeated exposure to anesthetic doses of ketamine. Administration of low-dose ketamine prior to full sedation prevented caspase-3 activation in the hippocampus and SCC. Primary cultures of cortical neurons treated with ketamine (10 mu M-10 mM) at 3 days-in vitro (3 DIV) displayed a concentration-dependent decrease in expanded growth cones. Furthermore, neuronal production and localization of ADNP varied as a function of both ketamine concentration and length of exposure. Taken together, these data support the model that ADNP induction may be partially responsible for the efficacy of a low-dose ketamine pre-treatment in preventing ketamine-induced neuronal cell death. (C) 2015 IBRO. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:31 / 40
页数:10
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