Zhu Ming-Di, Zhao Lin-Xia, Wang Xiao-Tian, Gao Yong-Jing, Zhang Zhi-Jun
Department of Orthopedics, Affiliated Hospital to Nantong University, Nantong 226001, China.
Pain Research Laboratory, Institute of Nautical Medicine, Jiangsu Key Laboratory of Neuroregeneration, Nantong University, Nantong 226001, China.
Brain Res Bull. 2014 Oct;109:54-60. doi: 10.1016/j.brainresbull.2014.10.002. Epub 2014 Oct 16.
Ligustilide is the main component of Danggui essential oil, and recently reported to have anti-inflammatory and neuroprotective effect. Increasing evidence suggests that glia-mediated neuroinflammation in the spinal cord plays a vital role in the pathogenesis of chronic pain. In the present study, we investigated the anti-inflammatory and anti-nociceptive effect of ligustilide both in vitro and in vivo. In microglial cell line BV2 cells, lipopolysaccharide (LPS) time-dependently increased the mRNA expression of proinflammatory cytokines (TNF-α, IL-1β, and IL-6), which was decreased by pretreatment with ligustilide in a dose-dependent manner. Ligustilide also decreased LPS-induced proinflammatory cytokines production in primary cultured microglia. In vivo, intrathecal injection of LPS induced mechanical allodynia in mice. Intravenous injection of ligustilide prevented LPS-induced mechanical allodynia, and decreased LPS-induced TNF-α, IL-1β, and IL-6 up-regulation in the spinal cord. In addition, repetitive intravenous injection of ligustilide attenuated intraplantar injection of complete Freund's adjuvant (CFA)-induced mechanical allodynia and thermal hyperalgesia. The same treatment of ligustilide also inhibited CFA-induced TNF-α, IL-1β, and IL-6 up-regulation and microglial activation in the spinal cord. Taken together, our data suggest that ligustilide can alleviate inflammatory pain partly through inhibition of microglial activation and proinflammatory cytokines production, which indicates a possible benefit from the use of ligustilide in the treatment of inflammatory pain and neuroinflammation-associated disorders.
藁本内酯是当归精油的主要成分,最近报道其具有抗炎和神经保护作用。越来越多的证据表明,脊髓中胶质细胞介导的神经炎症在慢性疼痛的发病机制中起着至关重要的作用。在本研究中,我们在体外和体内研究了藁本内酯的抗炎和抗伤害感受作用。在小胶质细胞系BV2细胞中,脂多糖(LPS)以时间依赖性方式增加促炎细胞因子(TNF-α、IL-1β和IL-6)的mRNA表达,而藁本内酯预处理以剂量依赖性方式降低了这种表达。藁本内酯还降低了原代培养小胶质细胞中LPS诱导的促炎细胞因子产生。在体内,鞘内注射LPS可诱导小鼠机械性异常性疼痛。静脉注射藁本内酯可预防LPS诱导的机械性异常性疼痛,并降低LPS诱导的脊髓中TNF-α、IL-1β和IL-6的上调。此外,重复静脉注射藁本内酯可减轻足底注射完全弗氏佐剂(CFA)诱导的机械性异常性疼痛和热痛觉过敏。藁本内酯的相同处理还抑制了CFA诱导的脊髓中TNF-α、IL-1β和IL-6的上调以及小胶质细胞活化。综上所述,我们的数据表明藁本内酯可部分通过抑制小胶质细胞活化和促炎细胞因子产生来减轻炎性疼痛,这表明使用藁本内酯治疗炎性疼痛和神经炎症相关疾病可能有益。