Lin Jiefu, Shen Fuyi, Lu Jing, Liang Feng, Zhang Yiying, Xie Zhongcong, Dong Yuanlin
Department of Anesthesiology, The First Affiliated Hospital of Jinan University, Guangzhou, China.
Geriatric Anesthesia Research Unit, Department of Anesthesia, Critical Care and Pain Medicine, Massachusetts General Hospital and Harvard Medical School, Charlestown, MA, United States.
Front Aging Neurosci. 2021 Jul 21;13:688587. doi: 10.3389/fnagi.2021.688587. eCollection 2021.
Anesthesia/surgery has been reported to be associated with perioperative neurocognitive disorder (PND) in patients and induces cognitive impairment in mice. Previous studies demonstrate cyclosporine A (CsA) attenuates the anesthesia/surgery-induced cognitive impairment in mice. However, CsA has immunosuppressive effects and may not be routinely used to prevent or treat PND in patients. WS635 is a nonimmunosuppressive CsA analog. We, therefore, set out to determine whether WS635 could mitigate the anesthesia/surgery-induced cognitive impairment in mice. We performed abdominal surgery under 1.4% isoflurane anesthesia (anesthesia/surgery) for 2 h in 9 month-old wild-type (WT) mice. We treated the mice with CsA (10 mg/kg) or different doses (13.2 mg/kg, 26.4 mg/kg and 52.8 mg/kg) of WS635 before and after the anesthesia/surgery. Barnes maze and fear conditioning system (FCS) were employed to evaluate the cognitive function in mice. We measured the amounts of postsynaptic density (PSD)-95, synaptophysin, and ATP in the hippocampus and cortex of the mice using western blot and ATP Colorimetric/Fluorometric Assay, respectively. We found that the treatment with 52.8 mg/kg, but not 13.2 mg/kg or 26.4 mg/kg, of WS635 attenuated the anesthesia/surgery-induced cognitive impairment in mice and the reductions in the amounts of PSD-95, synaptophysin, and ATP in the mice brain tissues. These results have established a system to study WS635 further and suggest that we need to perform more experiments to determine whether WS635 can ultimately be used as one of the interventions for PND in patients.
据报道,麻醉/手术与患者围手术期神经认知障碍(PND)相关,并可导致小鼠认知功能受损。先前的研究表明,环孢素A(CsA)可减轻麻醉/手术诱导的小鼠认知功能障碍。然而,CsA具有免疫抑制作用,可能无法常规用于预防或治疗患者的PND。WS635是一种非免疫抑制性的CsA类似物。因此,我们着手确定WS635是否能减轻麻醉/手术诱导的小鼠认知功能障碍。我们在9月龄野生型(WT)小鼠中,于1.4%异氟烷麻醉下进行腹部手术(麻醉/手术)2小时。在麻醉/手术前后,我们用CsA(10mg/kg)或不同剂量(13.2mg/kg、26.4mg/kg和52.8mg/kg)的WS635对小鼠进行治疗。采用巴恩斯迷宫和恐惧条件反射系统(FCS)评估小鼠的认知功能。我们分别使用蛋白质免疫印迹法和ATP比色/荧光测定法,测量小鼠海马体和皮质中突触后致密蛋白(PSD)-95、突触素和ATP的含量。我们发现,52.8mg/kg的WS635治疗可减轻麻醉/手术诱导的小鼠认知功能障碍以及小鼠脑组织中PSD-95、突触素和ATP含量的降低,而13.2mg/kg或26.4mg/kg的WS635则无此作用。这些结果建立了一个进一步研究WS635的系统,并表明我们需要进行更多实验,以确定WS635是否最终可作为患者PND的干预措施之一。