Alkaloids enriched extract from Dendrobium nobile Lindl. attenuates tau protein hyperphosphorylation and apoptosis induced by lipopolysaccharide in rat brain

被引:97
作者
Yang, Shu [1 ]
Gong, Qihai [1 ]
Wu, Qin [1 ]
Li, Fei [1 ]
Lu, Yuanfu [1 ]
Shi, Jingshan [1 ]
机构
[1] Zunyi Med Coll, Dept Pharmacol, Zunyi 563000, Guizhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Dendrobium nobile Lindl. alkaloids; Lipopolysaccharide; Tau protein; Hyperphosphorylation; Rat; ALZHEIMERS-DISEASE; PHOSPHORYLATED-TAU; NEUROINFLAMMATION; PATHOGENESIS; KINASE; EVENT; P38;
D O I
10.1016/j.phymed.2013.10.026
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Neurofibrillary tangles, one of the characteristic pathological features of Alzheimer's disease (AD), are composed of paired helical filaments mainly with hyperphosphorylated tau protein. Inhibition of the hyperphosphorylation of tau protein is an effective therapy for AD. The current study was designed to investigate the protective effects of alkaloids enriched extract from Dendrobium Nobile Lindl. (EDNLA), a Chinese medicinal herb, on hyperphosphorylation of tau protein in AD brain. Rats were administrated intragastrically with different doses of DNLA (20, 40 mg/kg) every 8 h for one day, followed by lipopolysaccharide (LPS, 100 mu,g) injecting into the bilateral ventricle. Two hours later, the hippocampi of each group were collected to examine the hyperphosphorylated tau protein by western blotting. Additional rats were treated by EDNLA thrice daily for one week, to examine the effects on LPS-induced apoptosis in the brain. LPS injection significantly increased the expression of hyperphosphorylated tau protein at Ser396, Ser199-202, Ser404, Thr231, Thr205 sites and GSK-3 beta increased, LPS also induced apoptosis in the brain. EDNLA dramatically ameliorated these abnormal changes (P <0.05). The present study demonstrated that EDNLA attenuates LPS-induced hyperphosphorylation of tau protein in rat's hippocampus and protects against LPS-induced apoptosis in rat brain. (C) 2013 Elsevier GmbH. All rights reserved.
引用
收藏
页码:712 / 716
页数:5
相关论文
共 25 条
[1]   Role of complement in neurodegeneration and neuroinflammation [J].
Bonifati, Domenico Marco ;
Kishore, Uday .
MOLECULAR IMMUNOLOGY, 2007, 44 (05) :999-1010
[2]  
Castellani RJ, 2008, J ALZHEIMERS DIS, V14, P377
[3]   Aberrant phosphorylation in the pathogenesis of Alzheimer's disease [J].
Chung, Sul-Hee .
BMB REPORTS, 2009, 42 (08) :467-474
[4]  
Czlonkowska Anna, 2002, Neurol Neurochir Pol, V36, P15
[5]   p38 mitogen activated protein kinase as a therapeutic target for Alzheimer's disease [J].
Dalrymple, SA .
JOURNAL OF MOLECULAR NEUROSCIENCE, 2002, 19 (03) :295-299
[6]   Neuroinflammation - An Early Event in Both the History and Pathogenesis of Alzheimer's Disease [J].
Eikelenboom, Piet ;
van Exel, Erik ;
Hoozemans, Jeroen J. M. ;
Veerhuis, Rob ;
Rozemuller, Annemieke J. M. ;
van Gool, Willem A. .
NEURODEGENERATIVE DISEASES, 2010, 7 (1-3) :38-41
[7]   PHOSPHORYLATION OF TAU PROTEINS - A MAJOR EVENT DURING THE PROCESS OF NEUROFIBRILLARY DEGENERATION - A COMPARATIVE-STUDY BETWEEN ALZHEIMERS-DISEASE AND DOWNS-SYNDROME [J].
FLAMENT, S ;
DELACOURTE, A ;
MANN, DMA .
BRAIN RESEARCH, 1990, 516 (01) :15-19
[8]  
Garcia Teresa, 2004, Gac Med Mex, V140, P329
[9]   Regulation of promoter activity of the APP gene by cytokines and growth factors - Implications in Alzheimer's disease [J].
Ge, YW ;
Lahiri, DK .
CELL SIGNALING, TRANSCRIPTION, AND TRANSLATION AS THERAPEUTIC TARGETS, 2002, 973 :463-467
[10]   Conformation of paired helical filaments blocks dephosphorylation of epitopes shared with fetal tau except Ser199/202 and Ser202/Thr205 [J].
Gordon-Krajcer, W ;
Yang, LS ;
Ksiezak-Reding, H .
BRAIN RESEARCH, 2000, 856 (1-2) :163-175