WS635 Attenuates the Anesthesia/Surgery-Induced Cognitive Impairment in Mice

被引:4
|
作者
Lin, Jiefu [1 ,2 ,3 ,4 ]
Shen, Fuyi [2 ,3 ,5 ]
Lu, Jing [2 ,3 ,6 ]
Liang, Feng [2 ,3 ]
Zhang, Yiying [2 ,3 ]
Xie, Zhongcong [2 ,3 ]
Dong, Yuanlin [2 ,3 ]
机构
[1] Jinan Univ, Affiliated Hosp 1, Dept Anesthesiol, Guangzhou, Peoples R China
[2] Massachusetts Gen Hosp, Dept Anesthesia Crit Care & Pain Med, Geriatr Anesthesia Res Unit, Charlestown, MA 02129 USA
[3] Harvard Med Sch, Charlestown, MA 02129 USA
[4] Sun Yat Sen Univ, Affiliated Shantou Hosp, Shantou Cent Hosp, Dept Anesthesiol, Shantou, Peoples R China
[5] Tongji Univ, Sch Med, Shanghai Matern & Infant Hosp 1, Dept Anesthesiol, Shanghai, Peoples R China
[6] Univ Elect Sci & Technol China, Sichuan Prov Peoples Hosp, Dept Anesthesiol, Chengdu, Peoples R China
来源
基金
美国国家卫生研究院;
关键词
cognitive impairment; WS635; synapse; ATP; anesthesia/surgery; SYNAPSE LOSS; PERMEABILITY TRANSITION; IDEBENONE; CYCLOSPORINE; DYSFUNCTION; INHIBITION; ISOFLURANE; PLASTICITY; DELIRIUM; SURGERY;
D O I
10.3389/fnagi.2021.688587
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
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.
引用
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页数:11
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