Zhang Ce, Zhang Yiying, Shen Yuan, Zhao Guoqing, Xie Zhongcong, Dong Yuanlin
Department of Anesthesia, China-Japan Union Hospital of Jilin University, Changchun, Jilin, P.R. China.
Geriatric Anesthesia Research Unit, Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, USA.
J Alzheimers Dis. 2017;57(2):505-518. doi: 10.3233/JAD-161268.
Anesthesia and/or surgery may promote Alzheimer's disease (AD) by accelerating its neuropathogenesis. Other studies showed different findings. However, the potential sex difference among these studies has not been well considered, and it is unknown whether male or female AD patients are more vulnerable to develop postoperative cognitive dysfunction. We therefore set out to perform a proof of concept study to determine whether anesthesia and surgery can have different effects in male and female AD transgenic (Tg) mice, and in female AD Tg plus Cyclophilin D knockout (CypD KO) mice. The mice received an abdominal surgery under sevoflurane anesthesia (anesthesia/surgery). Fear Conditioning System (FCS) was used to assess the cognitive function. Hippocampal levels of synaptic marker postsynaptic density 95 (PSD-95) and synaptophysin (SVP) were measured using western blot analysis. Here we showed that the anesthesia/surgery decreased the freezing time in context test of FCS at 7 days after the anesthesia/surgery in female, but not male, mice. The anesthesia/surgery reduced hippocampus levels of synaptic marker PSD-95 and SVP in female, but not male, mice. The anesthesia/surgery induced neither reduction in freezing time in FCS nor decreased hippocampus levels of PSD-95 and SVP in the AD Tg plus CypD KO mice. These data suggest that the anesthesia/surgery induced a sex-dependent cognitive impairment and reduction in hippocampus levels of synaptic markers in AD Tg mice, potentially via a mitochondria-associated mechanism. These findings could promote clinical investigations to determine whether female AD patients are more vulnerable to the development of postoperative cognitive dysfunction.
麻醉和/或手术可能通过加速神经病理发生过程来促进阿尔茨海默病(AD)的发展。其他研究则得出了不同的结果。然而,这些研究中潜在的性别差异尚未得到充分考虑,并且尚不清楚男性或女性AD患者是否更易发生术后认知功能障碍。因此,我们开展了一项概念验证研究,以确定麻醉和手术对雄性和雌性AD转基因(Tg)小鼠以及雌性AD Tg加亲环素D基因敲除(CypD KO)小鼠是否会产生不同影响。小鼠在七氟醚麻醉下接受腹部手术(麻醉/手术)。采用恐惧条件反射系统(FCS)评估认知功能。使用蛋白质免疫印迹分析测量海马中突触标志物突触后致密蛋白95(PSD - 95)和突触素(SVP)的水平。我们发现,在麻醉/手术后7天,麻醉/手术降低了雌性而非雄性小鼠FCS情境测试中的僵住时间。麻醉/手术降低了雌性而非雄性小鼠海马中突触标志物PSD - 95和SVP的水平。麻醉/手术在AD Tg加CypD KO小鼠中既未导致FCS中僵住时间减少,也未降低海马中PSD - 95和SVP的水平。这些数据表明,麻醉/手术在AD Tg小鼠中诱导了性别依赖性的认知障碍以及海马中突触标志物水平的降低,可能是通过一种与线粒体相关的机制。这些发现可能会推动临床研究,以确定女性AD患者是否更易发生术后认知功能障碍。