Zhang Tianrui, Liang Wulin, Zhang Mingqian, Cui Shuang, Huang Xiyan, Ou Wenjing, Huang Rikang, Gao Jiahui, Jia Zhanhong, Zhang Shuofeng
Department of Pharmacology of Traditional Chinese Medicine, College of Chinese Medicine, Beijing University of Chinese Medicine, Beijing 102488, China.
Pharmaceuticals (Basel). 2023 Feb 6;16(2):243. doi: 10.3390/ph16020243.
Neuropathic pain (NP) is a common pain disease that seriously affects the quality of life and physical and mental health of patients. Daphnetin is extracted from the Nitsche and has the structure of 7,8-dihydroxy coumarin. As a natural product, daphnetin displays a wide range of pharmacological activities, such as analgesia and anti-inflammatory activities, but whether it is able to improve NP through anti-inflammatory effects is unknown. Therefore, this paper intends to investigate the mechanism of daphnetin in improving NP rats affected by the intrathecal injection of tumor necrosis factor-α (TNF-α) from the perspective of anti-inflammation. Our results showed that daphnetin significantly improved hyperalgesia in NP rats. Daphnetin inhibited the activation and polarization of glial cells and neurons in the spinal cord of NP rats and reduced the expression of mRNA and protein of inflammatory factors and chemokine pairs in the spinal cord. Daphnetin inhibited the polarization of human microglia cell 3 (HMC3) cells and human glioma cells (U251) cells toward M1 microglia and A1 astrocytes, respectively, and induced the conversion of M1 microglia and A1 astrocytes to M2 microglia and A2 astrocytes, respectively. In conclusion, daphnetin ameliorates NP by inhibiting the expression of inflammatory factors and chemokines and the polarization of glial cells in the spinal cord of NP rats. This study provides a theoretical basis for the treatment of NP with daphnetin to expand the clinical application of daphnetin.
神经病理性疼痛(NP)是一种常见的疼痛疾病,严重影响患者的生活质量以及身心健康。瑞香素是从瑞香科植物中提取的,具有7,8 - 二羟基香豆素的结构。作为一种天然产物,瑞香素具有广泛的药理活性,如镇痛和抗炎活性,但它是否能够通过抗炎作用改善神经病理性疼痛尚不清楚。因此,本文旨在从抗炎角度研究瑞香素改善鞘内注射肿瘤坏死因子-α(TNF-α)所致神经病理性疼痛大鼠的机制。我们的结果表明,瑞香素显著改善了神经病理性疼痛大鼠的痛觉过敏。瑞香素抑制了神经病理性疼痛大鼠脊髓中胶质细胞和神经元的激活与极化,并降低了脊髓中炎症因子和趋化因子对的mRNA和蛋白表达。瑞香素分别抑制了人小胶质细胞3(HMC3)细胞和人胶质瘤细胞(U251)细胞向M1小胶质细胞和A1星形胶质细胞的极化,并诱导M1小胶质细胞和A1星形胶质细胞分别向M2小胶质细胞和A2星形胶质细胞转化。总之,瑞香素通过抑制神经病理性疼痛大鼠脊髓中炎症因子和趋化因子的表达以及胶质细胞的极化来改善神经病理性疼痛。本研究为瑞香素治疗神经病理性疼痛提供了理论依据,以扩大瑞香素的临床应用。