Fan Hongwei, Wu Zhenyu, Zhu DaYu, Gu Junxiang, Xu Mang, Zhang Mingzhe, Duan Haokai, Li Yunqing, Chen Tao
Department of Human Anatomy, Xuzhou Medical University, Xuzhou, China.
Department of Anatomy, Histology and Embryology, K. K. Leung Brain Research Centre, Fourth Military Medical University, Xi'an, China.
Front Neurosci. 2022 Feb 3;15:804722. doi: 10.3389/fnins.2021.804722. eCollection 2021.
Inflammatory pain is one of the most common symptoms of clinical pain that seriously affects patient quality of life, but it currently has limited therapeutic options. Proanthocyanidins, a group of polyphenols enriched in plants and foods, have been reported to exert anti-inflammatory pain-alleviating effects. However, the mechanism by which proanthocyanidins relieve inflammatory pain in the central nervous system is unclear. In the present study, we observed that intrathecal injection of proanthocyanidins inhibited mechanical and thermal pain sensitivity in mice with inflammatory pain induced by Complete Freund's Adjuvant (CFA) injection. Electrophysiological results further showed that proanthocyanidins inhibited the frequency of spontaneous excitatory postsynaptic currents without affecting the spontaneous inhibitory postsynaptic currents or the intrinsic properties of parabrachial nucleus-projecting neurons in the spinal cord. The effect of proanthocyanidins may be mediated by their inhibition of phosphorylated activation of the PI3K/Akt/mTOR pathway molecules in dorsal root ganglia neurons. In summary, intrathecal injection of procyanidin induces an obvious anti-inflammatory pain effect in mice by inhibiting peripheral excitatory inputs to spinal neurons that send nociceptive information to supraspinal areas.
炎性疼痛是临床疼痛最常见的症状之一,严重影响患者生活质量,但目前治疗选择有限。原花青素是一类富含于植物和食物中的多酚,据报道具有抗炎止痛作用。然而,原花青素在中枢神经系统中缓解炎性疼痛的机制尚不清楚。在本研究中,我们观察到鞘内注射原花青素可抑制完全弗氏佐剂(CFA)注射诱导的炎性疼痛小鼠的机械性和热痛敏感性。电生理结果进一步表明,原花青素可抑制自发兴奋性突触后电流的频率,而不影响自发抑制性突触后电流或脊髓中臂旁核投射神经元的内在特性。原花青素的作用可能是通过抑制背根神经节神经元中PI3K/Akt/mTOR通路分子的磷酸化激活来介导的。总之,鞘内注射原花青素通过抑制向脊髓上区域发送伤害性信息的脊髓神经元的外周兴奋性输入,在小鼠中诱导明显的抗炎止痛作用。