Zhang Shuai, Hu Xueyuan, Guan Wei, Luan Li, Li Bei, Tang Qichao, Fan Honggang
Department of Veterinary Medicine, College of Veterinary Medicine, Northeast Agricultural University, Harbin, China.
PLoS One. 2017 Apr 12;12(4):e0175654. doi: 10.1371/journal.pone.0175654. eCollection 2017.
Isoflurane anesthesia has been shown to be responsible for cognitive impairment in Alzheimer's disease (AD) and development of AD in the older age groups. However, the pathogenesis of AD-related cognitive impairments induced by isoflurane anesthesia remains elusive. Thus, this study was designed to investigate the mechanism by which isoflurane anesthesia caused AD-related cognitive impairments. Aged Wistar rats were randomly divided into 6 groups (n = 12), 1 control group (CONT) and 5 isoflurane treated (ISO) groups (ISO 0, ISO 0.5D, ISO 1D, ISO 3D and ISO 7D). The CONT group inhaled 30% O2 for 2 h without any anesthesia. ISO groups were placed under anesthesia with 3% isoflurane and then exposed to 1.5% isoflurane delivered in 30% O2 for 2 h. Rats in each ISO group were then analyzed immediately (ISO 0) or at various time points (0.5, 1, 3 or 7 day) after this exposure. Cognitive function was assessed using the Morris water maze test. Protein levels of amyloid precursor protein (APP), β-site APP cleavage enzyme-1 (BACE-1) and Aβ42 peptide were analyzed in hippocampal samples by Western blot. β-Amyloid (Abeta) plaques were detected in hippocampal sections by Congo red staining. Compared with controls, all ISO groups showed increased escape latency and impaired spatial memory. Isoflurane increased APP mRNA expression and APP protein depletion, promoting Aβ42 overproduction, oligomerization and accumulation. However, isoflurane did not affect BACE-1 expression. Abeta plaques were observed only in those ISO groups sacrificed at 3 or 7 d. Our data indicate that aged rats exposed to isoflurane had increased APP mRNA expression and APP protein depletion, with Aβ42 peptide overproduction and oligomerization, resulting in formation of Abeta plaques in the hippocampus. Such effects might have contributed to cognitive impairments, including in spatial memory, observed in these rats after isoflurane anesthesia.
异氟烷麻醉已被证明与阿尔茨海默病(AD)的认知障碍以及老年人群中AD的发展有关。然而,异氟烷麻醉诱导的AD相关认知障碍的发病机制仍不清楚。因此,本研究旨在探讨异氟烷麻醉导致AD相关认知障碍的机制。将老年Wistar大鼠随机分为6组(n = 12),1个对照组(CONT)和5个异氟烷处理组(ISO)(ISO 0、ISO 0.5D、ISO 1D、ISO 3D和ISO 7D)。CONT组吸入30%氧气2小时,无任何麻醉。ISO组用3%异氟烷麻醉,然后暴露于含30%氧气的1.5%异氟烷中2小时。然后,每个ISO组的大鼠在暴露后立即(ISO 0)或在不同时间点(0.5、1、3或7天)进行分析。使用莫里斯水迷宫试验评估认知功能。通过蛋白质印迹法分析海马样本中淀粉样前体蛋白(APP)、β-位点APP裂解酶-1(BACE-1)和Aβ42肽的蛋白质水平。通过刚果红染色在海马切片中检测β-淀粉样蛋白(Abeta)斑块。与对照组相比,所有ISO组的逃避潜伏期均延长,空间记忆受损。异氟烷增加APP mRNA表达和APP蛋白消耗,促进Aβ42的过量产生、寡聚化和积累。然而,异氟烷不影响BACE-1表达。仅在3或7天处死的ISO组中观察到Abeta斑块。我们的数据表明,暴露于异氟烷的老年大鼠APP mRNA表达增加,APP蛋白消耗增加,Aβ42肽过量产生和寡聚化,导致海马中形成Abeta斑块。这些效应可能导致了这些大鼠在异氟烷麻醉后出现的认知障碍,包括空间记忆障碍。