Lipid Emulsion Improves Functional Recovery in an Animal Model of Stroke

被引:17
|
作者
Tanioka, Motomasa [1 ,2 ]
Park, Wyun Kon [3 ]
Park, Joohyun [2 ,4 ]
Lee, Jong Eun [2 ,4 ]
Lee, Bae Hwan [1 ,2 ]
机构
[1] Yonsei Univ, Dept Physiol, Coll Med, Seoul 03722, South Korea
[2] Yonsei Univ, Coll Med, Brain Korea 21 PLUS Project Med Sci, Seoul 03722, South Korea
[3] Yonsei Univ, Anesthesia & Pain Res Inst, Dept Anesthesiol & Pain Med, Coll Med, Seoul 03722, South Korea
[4] Yonsei Univ, Dept Anat, Coll Med, Seoul 03722, South Korea
基金
新加坡国家研究基金会;
关键词
neuroprotection; stroke; ischemia; middle cerebral artery occlusion; reperfusion injury; lipid emulsion; excitotoxicity; ACUTE BRAIN-INJURY; CEREBRAL-ISCHEMIA; REPERFUSION INJURY; INDUCED ASYSTOLE; INTERLEUKIN-1; NEUROPROTECTION; RESUSCITATION; DYSFUNCTION; EXPRESSION; PROTECTION;
D O I
10.3390/ijms21197373
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Stroke is a life-threatening condition that leads to the death of many people around the world. Reperfusion injury after ischemic stroke is a recurrent problem associated with various surgical procedures that involve the removal of blockages in the brain arteries. Lipid emulsion was recently shown to attenuate ischemic reperfusion injury in the heart and to protect the brain from excitotoxicity. However, investigations on the protective mechanisms of lipid emulsion against ischemia in the brain are still lacking. This study aimed to determine the neuroprotective effects of lipid emulsion in an in vivo rat model of ischemic reperfusion injury through middle cerebral artery occlusion (MCAO). Under sodium pentobarbital anesthesia, rats were subjected to MCAO surgery and were administered with lipid emulsion through intra-arterial injection during reperfusion. The experimental animals were assessed for neurological deficit wherein the brains were extracted at 24 h after reperfusion for triphenyltetrazolium chloride staining, immunoblotting and qPCR. Neuroprotection was found to be dosage-dependent and the rats treated with 20% lipid emulsion had significantly decreased infarction volumes and lower Bederson scores. Phosphorylation of Akt and glycogen synthase kinase 3-beta (GSK3-beta) were increased in the 20% lipid-emulsion treated group. The Wnt-associated signals showed a marked increase with a concomitant decrease in signals of inflammatory markers in the group treated with 20% lipid emulsion. The protective effects of lipid emulsion and survival-related expression of genes such as Akt, GSK-3 beta, Wnt1 and beta-catenin were reversed by the intra-peritoneal administration of XAV939 through the inhibition of the Wnt/beta-catenin signaling pathway. These results suggest that lipid emulsion has neuroprotective effects against ischemic reperfusion injury in the brain through the modulation of the Wnt signaling pathway and may provide potential insights for the development of therapeutic targets.
引用
收藏
页码:1 / 21
页数:21
相关论文
共 50 条
  • [1] Cystamine Improves Functional Recovery via Axon Remodeling and Neuroprotection after Stroke in Mice
    Li, Pei-Cheng
    Jiao, Yun
    Ding, Jie
    Chen, Yu-Chen
    Cui, Ying
    Qian, Cheng
    Yang, Xiang-Yu
    Ju, Sheng-Hong
    Yao, Hong-Hong
    Teng, Gao-Jun
    CNS NEUROSCIENCE & THERAPEUTICS, 2015, 21 (03) : 231 - 240
  • [2] Cannabidiol reduces brain damage and improves functional recovery in a neonatal rat model of arterial ischemic stroke
    Ceprian, Maria
    Jimenez-Sanchez, Laura
    Vargas, Carlos
    Barata, Lorena
    Hind, Will
    Martinez-Orgado, Jose
    NEUROPHARMACOLOGY, 2017, 116 : 151 - 159
  • [3] Targeting GSNOR for functional recovery in a middle-aged mouse model of stroke
    Khan, Mushfiquddin
    Kumar, Pavan
    Qiao, Fei
    Islam, S. M. Touhidul
    Singh, Avtar K.
    Won, Je-Seong
    Feng, Wayne
    Singh, Inderjit
    BRAIN RESEARCH, 2020, 1741
  • [4] Dapoxetine prevents neuronal damage and improves functional outcomes in a model of ischemic stroke through the modulation of inflammation and oxidative stress
    Abdel-Hameed, Sarah Sameh
    El-Daly, Mahmoud
    Ahmed, Al-Shaimaa F.
    Bekhit, Amany A.
    Heeba, Gehan H.
    NAUNYN-SCHMIEDEBERGS ARCHIVES OF PHARMACOLOGY, 2024, 397 (01) : 253 - 266
  • [5] Paeoniflorin improves functional recovery through repressing neuroinflammation and facilitating neurogenesis in rat stroke model
    Tang, Hongli
    Wu, Leiruo
    Chen, Xixi
    Li, Huiting
    Huang, Baojun
    Huang, Zhenyang
    Zheng, Yiyang
    Zhu, Liqing
    Geng, Wujun
    PEERJ, 2021, 9
  • [6] Inhibition of ASIC1a Improves Behavioral Recovery after Stroke
    Armstrong, Ariel
    Yang, Tao
    Leng, Tiandong
    Xiong, Zhi-Gang
    ENEURO, 2024, 11 (02) : 16 - 16
  • [7] Stress as necessary component of realistic recovery in animal models of experimental stroke
    Walker, Frederick R.
    Jones, Kimberley A.
    Patience, Madeleine J.
    Zhao, Zidan
    Nilsson, Michael
    JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2014, 34 (02) : 208 - 214
  • [8] Poly-Arginine Peptide-18 (R18) Reduces Brain Injury and Improves Functional Outcomes in a Nonhuman Primate Stroke Model
    Meloni, Bruno P.
    Chen, Yining
    Harrison, Kathleen A.
    Nashed, Joseph Y.
    Blacker, David J.
    South, Samantha M.
    Anderton, Ryan S.
    Mastaglia, Frank L.
    Winterborn, Andrew
    Knuckey, Neville W.
    Cook, Douglas J.
    NEUROTHERAPEUTICS, 2020, 17 (02) : 627 - 634
  • [9] Intracerebral Transplantation of Autologous Mesenchymal Stem Cells Improves Functional Recovery in a Rat Model of Chronic Ischemic Stroke
    Myers, Max I.
    Hines, Kevin J.
    Gray, Andrew
    Spagnuolo, Gabrielle
    Rosenwasser, Robert
    Iacovitti, Lorraine
    TRANSLATIONAL STROKE RESEARCH, 2023, 16 (2) : 248 - 261
  • [10] Early treatment with minocycline following stroke in rats improves functional recovery and differentially modifies responses of peri-infarct microglia and astrocytes
    Yew, Wai Ping
    Djukic, Natalia D.
    Jayaseelan, Jaya S. P.
    Walker, Frederick R.
    Roos, Karl A. A.
    Chataway, Timothy K.
    Muyderman, Hakan
    Sims, Neil R.
    JOURNAL OF NEUROINFLAMMATION, 2019, 16 (1)