College of Medical Devices, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, China.
School of Life Science and Biopharmaceutics, Shenyang Pharmaceutical University, 103 Wenhua Road, Shenyang 110016, China.
Toxins (Basel). 2021 Jul 17;13(7):498. doi: 10.3390/toxins13070498.
Karsch (K), is a kind of traditional Chinese medicine, which has been used for a long history for the treatment of many diseases, such as inflammation, pain and cancer. In this study, DKK-SP1/2/3 genes were screened and extracted from the cDNA library of K. The DKK-SP1/2/3 were expressed by using plasmid pSYPU-1b in BL21, and recombinant proteins were obtained by column chromatography. In the xylene-induced mouse ear swelling and carrageenan-induced rat paw swelling model, DKK-SP1 exerted a significant anti-inflammatory effect by inhibiting the expression of Nav1.8 channel. Meanwhile, the release of pro-inflammatory cytokines (COX-2, IL-6) was decreased significantly and the release of anti-inflammatory cytokines (IL-10) were elevated significantly. Moreover, DKK-SP1 could significantly decrease the Nav1.8 current in acutely isolated rat DRG neurons. In the acetic acid-writhing and ION-CCI model, DKK-SP2 displayed significant analgesic activity by inhibiting the expression of the Nav1.7 channel. Moreover, DKK-SP2 could significantly inhibit the Nav1.7 current in the hNav1.7-CHO cells.
Karsch (K) 是一种中药,长期以来一直用于治疗许多疾病,如炎症、疼痛和癌症。在这项研究中,从 K 的 cDNA 文库中筛选并提取了 DKK-SP1/2/3 基因。通过质粒 pSYPU-1b 在 BL21 中表达 DKK-SP1/2/3,通过柱层析获得重组蛋白。在二甲苯诱导的小鼠耳肿胀和角叉菜胶诱导的大鼠足肿胀模型中,DKK-SP1 通过抑制 Nav1.8 通道的表达发挥显著的抗炎作用。同时,促炎细胞因子(COX-2、IL-6)的释放明显减少,抗炎细胞因子(IL-10)的释放明显增加。此外,DKK-SP1 可显著降低急性分离的大鼠 DRG 神经元中的 Nav1.8 电流。在醋酸扭体和 ION-CCI 模型中,DKK-SP2 通过抑制 Nav1.7 通道的表达显示出显著的镇痛活性。此外,DKK-SP2 可显著抑制 hNav1.7-CHO 细胞中的 Nav1.7 电流。