Polyphenols fromToona sinensissSeeds Alleviate Neuroinflammation Induced by 6-Hydroxydopamine Through Suppressing p38 MAPK Signaling Pathway in a Rat Model of Parkinson's Disease

被引:24
作者
Zhuang, Wenxin [1 ]
Cai, Meiyun [2 ]
Li, Wanzhong [3 ]
Chen, Chao [2 ]
Wang, Yanqiang [4 ]
Lv, E. [2 ]
Fu, Wenyu [2 ]
机构
[1] Weifang Med Univ, Ctr Expt Med Res, Weifang 261053, Shandong, Peoples R China
[2] Weifang Med Univ, Dept Histol & Embryol, Weifang 261053, Shandong, Peoples R China
[3] Weifang Med Univ, Dept Pharmaceut, Weifang 261053, Shandong, Peoples R China
[4] Weifang Med Univ, Dept Neurol, Affiliated Hosp, Weifang 261053, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Parkinson's disease; Neuroinflammation; Polyphenols fromtoona sinensisseeds; p38; MAPK; OXIDATIVE STRESS; DOPAMINERGIC NEURODEGENERATION; INDUCED INFLAMMATION; INHIBITING ERK1/2; CELLS; INVOLVEMENT; ACTIVATION; QUERCETIN; APOPTOSIS; EXTRACT;
D O I
10.1007/s11064-020-03067-2
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
Polyphenols fromToona sinensisseeds (PTSS) have demonstrated anti-inflammatory effects in various diseases, while the anti-neuroinflammatory effects still remain to be investigated. We aimed to investigate the effects of PTSS on Parkinson's disease and underlying mechanisms using a rat model. We employed 6-hydroxydopamine (6-OHDA) to male Sprague Dawley (SD) rats and PC12 cells to construct the in vivo and vitro models of PD and dopaminergic (DA) neuron injury, respectively. Cell viability was detected by cell counting kit-8 (CCK-8) assay and protein levels of inflammatory mediators and some p38 MAPK pathway molecules were investigated by immunohistochemistry and Western blot analyses. The results showed that 6-OHDA significantly increased protein levels of inflammatory mediators, such as cyclooxygenase-2 (COX-2), inducible nitric oxide synthase (iNOS), and tumor necrosis factor alpha (TNF-alpha), which could be reversed by PTSS through suppressing the p38 MAPK pathway. The anti-inflammatory effects of PTSS were significantly enhanced by the specific p38 inhibitor of SB203580 in vitro. The present work suggests that PTSS can exert anti-inflammatory effects on PD models, which may be attributed to the suppression of p38 MAPK signaling pathway.
引用
收藏
页码:2052 / 2064
页数:13
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