NR2B在七氟醚麻醉致老年大鼠认知功能障碍中的作用

Jingjing Jiang, Heng Li, Baojun Fu, Weihua Liu, Zonghang Lin
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摘要

目的探讨含2B NMDA受体(NR2B)在七氟醚麻醉诱导老年大鼠认知功能障碍中的作用。方法32只健康雄性Sprague-Dawley大鼠,18个月龄,体重570-630g,采用随机数表法分为4组(每组8只):对照组(C组)、七氟醚麻醉组(S组)、七氟烷麻醉加NR2B特异性抑制剂Ro 25-6981组(S+Ro组)和Ro 25-691组(Ro组)。S和S+RO组吸入3%七氟醚4h。S+RO在吸入七氟醚前15min腹膜内注射RO 25-6981 1mg/kg。麻醉结束后2天进行Morris水迷宫试验以评估认知功能。然后处死大鼠,获得海马组织,通过蛋白质印迹测定ERK1/2的表达和磷酸化。结果与C组相比,S组的逃逸潜伏期显著延长,穿越原平台的频率降低,停留在原平台象限的时间缩短,ERK1/2磷酸化水平降低(P<0.05),结论七氟醚麻醉诱导老年大鼠认知功能障碍的机制与上调NR2B表达和抑制ERK1/2活性有关。关键词:受体,N-甲基-D-天冬氨酸;麻醉剂、吸入;认知障碍;老化
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Role of NR2B in sevoflurane anesthesia-induced cognitive dysfunction in aged rats
Objective To evaluate the role of 2B-containing NMDA receptors (NR2B) in sevoflurane anesthesia-induced cognitive dysfunction in aged rats. Methods Thirty-two healthy male Sprague-Dawley rats, aged 18 months, weighing 570-630 g, were divided into 4 groups (n=8 each) using a random number table method: control group (group C), sevoflurane anesthesia group (group S), sevoflurane anesthesia plus NR2B specific inhibitor Ro 25-6981 group (group S+ RO) and Ro 25-6981 group (group RO). S and S+ RO groups inhaled 3% sevoflurane for 4 h. Ro 25-6981 1 mg/kg was intraperitoneally injected at 15 min before inhaling sevoflurane in group S+ RO.Morris water maze test was performed at 2 days after the end of anesthesia to assess cognitive function.The rats were then sacrificed, and hippocampal tissues were obtained for determination of the expression and phosphorylation of ERK1/2 by Western blot. Results Compared with group C, the escape latency was significantly prolonged, the frequency of crossing the original platform was reduced, the time of staying at the original platform quadrant was shortened, and the phosphorylation of ERK1/2 was decreased in group S (P 0.05). Compared with group S, the escape latency was significantly shortened, the frequency of crossing the original platform was increased, the time of staying at the original platform quadrant was prolonged, and the phosphorylation of ERK1/2 was increased in group S+ RO(P 0.05). Conclusion The mechanism by which sevoflurane anesthesia induces cognitive dysfunction is related to up-regulating the expression of NR2B and inhibiting the activity of ERK1/2 in aged rats. Key words: Receptors, N-methyl-D-aspartate; Anesthetics, inhalation; Cognition disorders; Aged
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中华麻醉学杂志
中华麻醉学杂志 Medicine-Anesthesiology and Pain Medicine
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