中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Neonatal exposure to ketamine disrupts developmental synapse unsilencing and predisposes adult mice for stressor-evoked anxiety

文献类型:期刊论文

作者Zhang, Xiaoyun2,3; Kong, Yue1,2,3; He, Guiqin3; Zhou, Zikai1,3,4
刊名NEUROPHARMACOLOGY
出版日期2020-12-01
卷号180页码:12
关键词Stress Anxiety Silent synapse Long-term potentiation Anesthesia
ISSN号0028-3908
DOI10.1016/j.neuropharm.2020.108300
通讯作者Zhang, Xiaoyun(xiaoyun_zhang@seu.edu.cn) ; Zhou, Zikai(zhouzikai@simm.ac.cn)
英文摘要Accumulating evidence suggests long-lasting impairments in brain development and cognition caused by neonatal exposure to general anesthetics. To date, very little is known about potential abnormal psychiatric manifestations attributable to neonatal anesthesia. In this study, we used ketamine to induce anesthesia in neonatal mice. By applying mild stressors one day before behavioral tests, we found that adult mice exhibit significant anxiety-like behaviors that were indistinguishable at basal level. Recruitment of AMPA (a-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid) type glutamate receptors into silent synapses is a prominent cellular process during neonatal neurodevelopment. We found that exposure to ketamine significantly disrupted synapse unsilencing, and impaired the expression of unsilencing-mediated long-term potentiation (LTP). Pharmacologically enhancement of neural activities by AMPAkine drug CX546 [1-(1,4-benzodioxan-6-ylcarbonyl) piperidine] effectively rescued disrupted developmental synapse unsilencing and LTP at neonatal age, and prevented stressor-evoked anxiety-like behaviors in adult mice. Together, our results indicate that neonatal exposure to ketamine may predispose individuals for psychiatric conditions via disrupting synapse unsilencing, and potentiation of neural activities during the anesthesia-recovery period may be an effective approach to manage adverse effects on brain development. This article is part of the special issue on 'Stress, Addiction and Plasticity'.
WOS关键词AWAKE-REGIONAL ANESTHESIA ; LONG-TERM POTENTIATION ; SILENT SYNAPSES ; GENERAL-ANESTHESIA ; INFANCY GAS ; SEVOFLURANE ; EXPRESSION ; PLASTICITY ; PERIOD ; MULTICENTER
资助项目National Natural Science Foundation of China[81971022] ; National Natural Science Foundation of China[31571040] ; Program of Shanghai Academic Research Leader[19XD1423300] ; Shanghai Municipal Commission of Education-Gaofeng Clinical Medicine[20191835]
WOS研究方向Neurosciences & Neurology ; Pharmacology & Pharmacy
语种英语
WOS记录号WOS:000593895300007
出版者PERGAMON-ELSEVIER SCIENCE LTD
源URL[http://119.78.100.183/handle/2S10ELR8/296209]  
专题中国科学院上海药物研究所
通讯作者Zhang, Xiaoyun; Zhou, Zikai
作者单位1.Chinese Acad Sci, Shanghai Inst Mat Med, Shanghai, Peoples R China
2.Southeast Univ, Inst Life Sci, Key Lab Dev Genes & Human Dis, Minist Educ, Nanjing, Peoples R China
3.Shanghai Jiao Tong Univ, Shanghai Mental Hlth Ctr, Shanghai Key Lab Psychot Disorders, Sch Med, Shanghai, Peoples R China
4.Nantong Univ, Coinnovat Ctr Neuroregenerat, Nantong, Peoples R China
推荐引用方式
GB/T 7714
Zhang, Xiaoyun,Kong, Yue,He, Guiqin,et al. Neonatal exposure to ketamine disrupts developmental synapse unsilencing and predisposes adult mice for stressor-evoked anxiety[J]. NEUROPHARMACOLOGY,2020,180:12.
APA Zhang, Xiaoyun,Kong, Yue,He, Guiqin,&Zhou, Zikai.(2020).Neonatal exposure to ketamine disrupts developmental synapse unsilencing and predisposes adult mice for stressor-evoked anxiety.NEUROPHARMACOLOGY,180,12.
MLA Zhang, Xiaoyun,et al."Neonatal exposure to ketamine disrupts developmental synapse unsilencing and predisposes adult mice for stressor-evoked anxiety".NEUROPHARMACOLOGY 180(2020):12.

入库方式: OAI收割

来源:上海药物研究所

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