兴奋性突触后电位
伤害
原花青素
脊髓
PI3K/AKT/mTOR通路
抑制性突触后电位
神经科学
药理学
突触后电位
中枢神经系统
医学
化学
内科学
多酚
生物
信号转导
生物化学
受体
抗氧化剂
作者
Hongwei Fan,Zhen-Yu Wu,Da-Yu Zhu,Junxiang Gu,Mang Xu,Mingzhe Zhang,Hao-Kai Duan,Yun-Qing Li,Tao Chen
标识
DOI:10.3389/fnins.2021.804722
摘要
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.
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