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右美托咪定通过调节新生大鼠谷氨酸对异氟烷诱导的神经元损伤的神经保护作用。

Neuroprotective effects of dexmedetomidine against isoflurane-induced neuronal injury via glutamate regulation in neonatal rats.

作者信息

Wang Xue, Shan Yangyang, Tang Zhiyin, Gao Linlin, Liu Hongtao

机构信息

Department of Anesthesiology, Shengjing Hospital, China Medical University, Shenyang 110004, China,

Department of Anesthesiology, Xiangyang Central Hospital, Affiliated Hospital of Hubei University of Arts and Sciences, Xiangyang 441000, China.

出版信息

Drug Des Devel Ther. 2018 Dec 21;13:153-160. doi: 10.2147/DDDT.S163197. eCollection 2019.

Abstract

BACKGROUND

Considerable evidences support the finding that the anesthesia reagent isoflurane increases neuronal cell death in young rats. Recent studies have shown that dexmedetomidine can reduce isoflurane-induced neuronal injury, but the mechanism remains unclear. We investigated whether isoflurane cause neurotoxicity to the central nervous system by regulating the N-methyl-D-aspartate receptor (NMDAR) and excitatory amino acid transporter1 (EAAT1) in young rats. Furthermore, we examined if dexmedetomidine could decrease isoflurane-induced neurotoxicity.

METHODS

Neonatal rats (postnatal day 7, n=144) were randomly divided into four groups of 36 animals each: control (saline injection without isoflurane); isoflurane (2% for 4 h); isoflurane + single dose of dexmedetomidine (75 µg/kg, 20 min before the start of 2% isoflurane for 4 h); and isoflurane + dual doses of dexmedetomidine (25 µg/kg, 20 min before and 2 h after start of isoflurane at 2% for 4 h). Six neonates from each group were euthanatized at 2 h, 12 h, 24 h, 3 days, 7 days and 28 days post-anesthesia. Hippocampi were collected and processed for protein extraction. Expression levels of the NMDAR subunits NR2A and NR2B, EAAT1 and caspase-3 were measured by western blot analysis.

RESULTS

Protein levels of NR2A, EAAT1 and caspase-3 were significantly increased in hippocampus of the isoflurane group from 2 h to 3 days, while NR2B levels were decreased. However, the -induced increase in NR2A, EAAT1 and caspase-3 and the decrease in NR2B in isoflurane-exposed rats were ameliorated in the rats treated with single or dual doses of dexmedetomidine. Isoflurane-induced neuronal damage in neonatal rats is due in part to the increase in NR2A and EAAT1 and the decrease in NR2B in the hippocampus.

CONCLUSION

Dexmedetomidine protects the brain against the use of isoflurane through the regulation of NR2A, NR2B and EAAT1. However, using the same amount of dexmedetomidine, the trend of protection is basically the same.

摘要

背景

大量证据支持麻醉剂异氟烷会增加幼鼠神经元细胞死亡这一发现。最近的研究表明右美托咪定可减轻异氟烷诱导的神经元损伤,但其机制仍不清楚。我们研究了异氟烷是否通过调节幼鼠的N-甲基-D-天冬氨酸受体(NMDAR)和兴奋性氨基酸转运体1(EAAT1)对中枢神经系统产生神经毒性。此外,我们还研究了右美托咪定是否能减轻异氟烷诱导的神经毒性。

方法

新生大鼠(出生后第7天,n = 144)随机分为四组,每组36只动物:对照组(注射生理盐水,未使用异氟烷);异氟烷组(2%,持续4小时);异氟烷 + 单剂量右美托咪定组(75 μg/kg,在开始使用2%异氟烷前20分钟注射,持续4小时);异氟烷 + 双剂量右美托咪定组(25 μg/kg,在开始使用2%异氟烷前20分钟及开始后2小时各注射一次,持续4小时)。每组在麻醉后2小时、12小时、24小时、3天、7天和28天各安乐死6只新生大鼠。收集海马体并进行蛋白质提取。通过蛋白质印迹分析测量NMDAR亚基NR2A和NR2B、EAAT1和半胱天冬酶-3的表达水平。

结果

异氟烷组海马体中NR2A、EAAT1和半胱天冬酶-3的蛋白质水平在2小时至3天显著升高,而NR2B水平降低。然而,在单剂量或双剂量右美托咪定处理的大鼠中,异氟烷暴露大鼠中NR​​A、EAAT1和半胱天冬酶-3的诱导增加以及NR2B的降低得到改善。异氟烷诱导新生大鼠神经元损伤部分归因于海马体中NR2A和EAAT1的增加以及NR2B的减少。

结论

右美托咪定通过调节NR2A、NR2B和EAAT1保护大脑免受异氟烷的影响。然而,使用相同剂量的右美托咪定,保护趋势基本相同。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/37f8/6306062/732571bcb0a3/dddt-13-153Fig1.jpg

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