Administration of chlorogenic acid alleviates spinal cord injury via TLR4/NF-B and p38 signaling pathway anti-inflammatory activity

被引:56
作者
Chen, Dayong [1 ]
Pan, Dan [1 ]
Tang, Shaolong [1 ]
Tan, Zhihong [1 ]
Zhang, Yanan [1 ]
Fu, Yunfeng [1 ]
Lue, Guohua [1 ]
Huang, Qinghua [1 ]
机构
[1] Cent Hosp Zhuzhou City, Dept Spine Surg, 116 Changjiang South Rd, Zhuzhou 412000, Hunan, Peoples R China
关键词
chlorogenic acid; spinal cord injury; inflammation; nuclear factor-B; p38; NF-KAPPA-B; NEUROPATHIC PAIN; INFLAMMATION; ACTIVATION; OXYGEN; DAMAGE; MODEL;
D O I
10.3892/mmr.2017.7987
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chlorogenic acid, as a secondary metabolite of plants, exhibits a variety of effects including free radical scavenging, antiseptic, anti-inflammatory and anti-viral, in addition to its ability to reduce blood glucose, protect the liver and act as an anti-hyperlipidemic agent and cholagogue. The present study demonstrated that administration of chlorogenic acid alleviated spinal cord injury (SCI) via anti-inflammatory activity mediated by nuclear factor (NF)-B and p38 signaling pathways. Wistar rats were used to structure a SCI model rat to explore the effects of administration of chlorogenic acid on SCI. The Basso, Beattie and Bresnahan test was executed for assessment of neuronal functional recovery and then spinal cord tissue wet/dry weight ratio was recorded. The present study demonstrated that chlorogenic acid increased SCI-inhibition of BBB scores and decreased SCI-induction of spinal cord wet/dry weight ratio in rats. In addition, chlorogenic acid suppressed SCI-induced inflammatory activity, inducible nitric oxide synthase activity and cyclooxygenase-2 protein expression in the SCI rat. Furthermore, chlorogenic acid suppressed Toll like receptor (TLR)-4/myeloid differentiation primary response 88 (MyD88)/NF-B/IB signaling pathways and downregulated p38 mitogen activated protein kinase protein expression in SCI rats. The findings suggest that administration of chlorogenic acid alleviates SCI via anti-inflammatory activity mediated by TLR4/MyD88/NF-B and p38 signaling pathways.
引用
收藏
页码:1340 / 1346
页数:7
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