RETRACTED: Sanhua Decoction, a Classic Herbal Prescription, Exerts Neuroprotection Through Regulating Phosphorylated Tau Level and Promoting Adult Endogenous Neurogenesis After Cerebral Ischemia/Reperfusion Injury

被引:18
作者
Fu, Deng-Lei [1 ,2 ]
Li, Ji-Huang [1 ,2 ]
Shi, Yi-Hua [1 ,2 ]
Zhang, Xi-Le [1 ,2 ]
Lin, Yan [1 ,2 ]
Zheng, Guo-Qing [1 ,2 ]
机构
[1] Wenzhou Med Univ, Dept Neurol, Affiliated Hosp 2, Wenzhou, Peoples R China
[2] Wenzhou Med Univ, Dept Neurol, Yuying Childrens Hosp, Wenzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
traditional Chinese medicine; ischemic stroke; endogenous neurogenesis; tau phosphorylation; neurological function recovery; ACUTE ISCHEMIC-STROKE; HEALTH-CARE PROFESSIONALS; STEM-CELL TRANSPLANTATION; FOREBRAIN NEUROGENESIS; SUBVENTRICULAR ZONE; ARTERY OCCLUSION; BRAIN; REELIN; ASTROCYTES; MIGRATION;
D O I
10.3389/fphys.2020.00057
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
Background: Ischemia stroke is the leading cause of death and long-term disability. Sanhua Decoction (SHD), a classic Chinese herbal prescription, has been used for ischemic stroke for about thousands of years. Here, we aim to investigate the neuroprotective effects of SHD on cerebral ischemia/reperfusion (CIR) injury rat models. Methods: The male Sprague-Dawley rats (body weight, 250-280 g; age, 7-8 weeks) were randomly divided into sham group, CIR group, and SHD group and were further divided into subgroups according to different time points at 6 h, 1, 3, 7, 14, 21, and 28 d, respectively. The SHD group received intragastric administration of SHD at 10 g kg(-1) d(-1). The focal CIR models were induced by middle cerebral artery occlusion according to Longa's method, while sham group had the same operation without suture insertion. Neurological deficit score (NDS) was evaluated using the Longa's scale. BrdU, doublecortin (DCX), and glial fibrillary acidic protein (GFAP) were used to label proliferation, migration, and differentiation of nerve cells before being observed by immunofluorescence. The expression of reelin, total tau (t-tau), and phosphorylated tau (p-tau) were evaluated by western blot and RT-qPCR. Results: SHD can significantly improve NDS at 1, 3, 7, and 14 d (p < 0.05), increase the number of BrdU positive and BrdU/DCX positive cells in subventricular zone at 3, 7, and 14 d (p < 0.05), upregulate BrdU/GFAP positive cells in the ischemic penumbra at 28 d after CIR (p < 0.05), and reduce p-tau level at 1, 3, 7, and 14 d (p < 0.05). There was no significant difference on reelin and t-tau level between three groups at each time points after CIR. Conclusions: SHD exerts neuroprotection probably by regulating p-tau level and promoting the proliferation, migration, and differentiation of endogenous neural stem cells, accompanying with neurobehavioral recovery.
引用
收藏
页数:11
相关论文
共 68 条
[1]   Astrocyte-endothelial interactions at the blood-brain barrier [J].
Abbott, NJ ;
Rönnbäck, L ;
Hansson, E .
NATURE REVIEWS NEUROSCIENCE, 2006, 7 (01) :41-53
[3]   Neurogenesis in the aging brain [J].
Apple, Deana M. ;
Solano-Fonseca, Rene ;
Kokovay, Erzsebet .
BIOCHEMICAL PHARMACOLOGY, 2017, 141 :77-85
[4]   Role of tau protein in both physiological and pathological conditions [J].
Avila, J ;
Lucas, JJ ;
Pérez, M ;
Hernández, F .
PHYSIOLOGICAL REVIEWS, 2004, 84 (02) :361-384
[5]   Mechanism of Tau Hyperphosphorylation Involving Lysosomal Enzyme Asparagine Endopeptidase in a Mouse Model of Brain Ischemia [J].
Basurto-Islas, Gustavo ;
Gu, Jin-Hua ;
Tung, Yunn Chyn ;
Liu, Fei ;
Iqbal, Khalid .
JOURNAL OF ALZHEIMERS DISEASE, 2018, 63 (02) :821-833
[6]   Brain Energy Metabolism: Focus on Astrocyte-Neuron Metabolic Cooperation [J].
Belanger, Mireille ;
Allaman, Igor ;
Magistretti, Pierre J. .
CELL METABOLISM, 2011, 14 (06) :724-738
[7]   Docosanoids Promote Neurogenesis and Angiogenesis, Blood-Brain Barrier Integrity, Penumbra Protection, and Neurobehavioral Recovery After Experimental Ischemic Stroke [J].
Belayev, Ludmila ;
Hong, Sung-Ha ;
Menghani, Hemant ;
Marcell, Shawn J. ;
Obenaus, Andre ;
Freitas, Raul S. ;
Khoutorova, Larissa ;
Balaszczuk, Veronica ;
Jun, Bokkyoo ;
Oria, Reinaldo B. ;
Bazan, Nicolas G. .
MOLECULAR NEUROBIOLOGY, 2018, 55 (08) :7090-7106
[8]   Effects of alteplase on survival after ischaemic stroke (IST-3): 3 year follow-up of a randomised, controlled, open-label trial [J].
Berge, Eivind ;
Cohen, Geoffrey ;
Roaldsen, Melinda B. ;
Lundstrom, Erik ;
Isaksson, Eva ;
Rudberg, Ann-Sofie ;
Slot, Karsten Bruins ;
Forbes, John ;
Smith, Joel ;
Drever, Jonathan ;
Wardlaw, Joanna M. ;
Lindley, Richard I. ;
Sandercock, Peter A. G. ;
Whiteley, William N. .
LANCET NEUROLOGY, 2016, 15 (10) :1028-1034
[9]   Neural stem cell transplantation in ischemic stroke: A role for preconditioning and cellular engineering [J].
Bernstock, Joshua D. ;
Peruzzotti-Jametti, Luca ;
Ye, Daniel ;
Gessler, Florian A. ;
Maric, Dragan ;
Vicario, Nunzio ;
Lee, Yang-Ja ;
Pluchino, Stefano ;
Hallenbeck, John M. .
JOURNAL OF CEREBRAL BLOOD FLOW AND METABOLISM, 2017, 37 (07) :2314-2319
[10]   Tau exacerbates excitotoxic brain damage in an animal model of stroke [J].
Bi, Mian ;
Gladbach, Amadeus ;
van Eersel, Janet ;
Ittner, Arne ;
Przybyla, Magdalena ;
van Hummel, Annika ;
Chua, Sook Wern ;
van der Hoven, Julia ;
Lee, Wei S. ;
Mueller, Julius ;
Parmar, Jasneet ;
von Jonquieres, Georg ;
Stefen, Holly ;
Guccione, Ernesto ;
Fath, Thomas ;
Housley, Gary D. ;
Klugmann, Matthias ;
Ke, Yazi D. ;
Ittner, Lars M. .
NATURE COMMUNICATIONS, 2017, 8