Delayed administration IL-1β neutralizing antibody improves cognitive function after transient global ischemia in rats

被引:6
作者
Zhao, Bei [1 ]
Zou, Chang-jiang [2 ]
Zhou, Ping [1 ]
机构
[1] Dali Univ, Sch Basic Med Sci, Dept Physiol & Pathophysiol, 2 Snowman Rd, Dali 671000, Yunnan, Peoples R China
[2] Peking Univ, Dept Physiol, Sch Med, 38 Xueyuan Rd, Beijing 100191, Peoples R China
基金
中国国家自然科学基金;
关键词
IL-1; beta; Ischemia; Cognitive function; Motor function; Delayed administration; THERAPEUTIC STRATEGIES; CEREBRAL-ISCHEMIA; STROKE; INFLAMMATION; MECHANISMS; DAMAGE; INTERLEUKIN-1-BETA; CONSEQUENCES; PROTECTION; MICROGLIA;
D O I
10.1016/j.bbr.2016.01.028
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
In order to study the protective effects on motor and cognitive function by inhibiting IL-1 beta as delayed as 24 h after global ischemia, we designed behavioral testing protocol and histology detection after 10 min transient global ischemia followed by IL-1 beta or its antibody intracerebroventricular injection. We found benefit of IL-1 beta antibody treatment 24 h after ischemia in cognitive function recovery. But no obvious amelioration in motor function was found. Further we detected cell morphology and survival by histology staining and proved IL-1 beta antibody could reduce ischemia induced cell morphological changes and cell loss in hippocampus, which related with cognitive function. Present results indicate intervening IL-1 beta pathway could be helpful in cognitive function recovery even as late as 24 h after ischemia happens. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:53 / 60
页数:8
相关论文
共 32 条
[1]   Inhibition of the inflammasome complex reduces the inflammatory response after thromboembolic stroke in mice [J].
Abulafia, Denise P. ;
Vaccari, Juan Pablo de Rivero ;
Lozano, J. Diego ;
Lotocki, George ;
Keane, Robert W. ;
Dietrich, W. Dalton .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2009, 29 (03) :534-544
[2]   Inflammation in Ischemic Stroke: Mechanisms, Consequences and Possible Drug Targets [J].
Ahmad, Muzamil ;
Dar, Nawab J. ;
Bhat, Zubair S. ;
Hussain, Aehtesham ;
Shah, Ayatullah ;
Liu, Hao ;
Graham, Steven H. .
CNS & NEUROLOGICAL DISORDERS-DRUG TARGETS, 2014, 13 (08) :1378-1396
[3]   Therapeutic strategies to improve drug delivery across the blood-brain barrier [J].
Azad, Tej D. ;
Pan, James ;
Connolly, Ian D. ;
Remington, Austin ;
Wilson, Christy M. ;
Grant, Gerald A. .
NEUROSURGICAL FOCUS, 2015, 38 (03)
[4]  
Beaulieu C, 1999, ANN NEUROL, V46, P568, DOI 10.1002/1531-8249(199910)46:4<568::AID-ANA4>3.0.CO
[5]  
2-R
[6]   INTRANASAL ADMINISTRATION OF GLIAL-DERIVED NEUROTROPHIC FACTOR (GDNF) RAPIDLY AND SIGNIFICANTLY INCREASES WHOLE-BRAIN GDNF LEVEL IN RATS [J].
Bender, T. S. ;
Migliore, M. M. ;
Campbell, R. B. ;
Gatley, S. John ;
Waszczak, B. L. .
NEUROSCIENCE, 2015, 303 :569-576
[7]   Effect of Needle Insertion Speed on Tissue Injury, Stress, and Backflow Distribution for Convection-Enhanced Delivery in the Rat Brain [J].
Casanova, Fernando ;
Carney, Paul R. ;
Sarntinoranont, Malisa .
PLOS ONE, 2014, 9 (04)
[8]   Inflammasome Signaling At The Heart Of Central Nervous System Pathology [J].
Chakraborty, Swarupa ;
Kaushik, Deepak Kumar ;
Gupta, Malvika ;
Basu, Anirban .
JOURNAL OF NEUROSCIENCE RESEARCH, 2010, 88 (08) :1615-1631
[9]   Neutralizing anti-interleuldn-1β antibodies modulate fetal blood-brain barrier function after ischemia [J].
Chen, Xiaodi ;
Sadowska, Grazyna B. ;
Zhang, Jiyong ;
Kim, Jeong-Eun ;
Cummings, Erin E. ;
Bodge, Courtney A. ;
Lim, Yow-Pin ;
Makeyev, Oleksandr ;
Besio, Walter G. ;
Gaitanis, John ;
Threlkeld, Steven W. ;
Banks, William A. ;
Stonestreet, Barbara S. .
NEUROBIOLOGY OF DISEASE, 2015, 73 :118-129
[10]   Interleukin-1 beta and tumor necrosis factor-alpha are expressed by different subsets of microglia and macrophages after ischemic stroke in mice [J].
Clausen, Bettina H. ;
Lambertsen, Kate L. ;
Babcock, Alicia A. ;
Holm, Thomas H. ;
Dagnaes-Hansen, Frederik ;
Finsen, Bente .
JOURNAL OF NEUROINFLAMMATION, 2008, 5 (1)