Department of Molecular and Cellular Physiology, Yamaguchi University Graduate School of Medicine, 1-1-1 Minami-Kogushi, Ube, 755-8505, Japan.
Department of Advanced Preventive Medicine, School of Medicine, Yamaguchi University, 1-1-1 Minami-Kogushi, Ube, 755-8505, Japan.
J Pharmacol Sci. 2022 Aug;149(4):189-197. doi: 10.1016/j.jphs.2022.05.002. Epub 2022 May 13.
We previously discovered that the SPC/Fyn/Rho-kinase (ROK) pathway mediates the Ca-sensitization of coronary arterial smooth muscle (CASM) contraction leading to vasospasm, a major cause of sudden death. Lately, we have been trying to find and develop more natural edible compounds which can treat and/or prevent the SPC-induced abnormal CASM contraction, and finally the first to discover that tangeretin (5,6,7,8,4'-pentamethoxyflavone), a natural compound extracted from citrus plants, can inhibit the SPC-induced CASM contraction both in the pretreatment and posttreatment. In porcine CASM tissues, tangeretin showed remarkable inhibitory effects on the SPC-induced contraction with modest inhibitory effects on the high K-depolarization-induced Ca-dependent contraction, both in pretreatment and posttreatment at the optimal concentrations; Regarding the mechanisms, tangeretin markedly abolished the SPC-induced cell contraction through inhibiting the SPC-induced activation and translocation of Fyn and ROK from the cytoplasm to the cell membrane in cultured CASM cells, resulting in the reduction of phosphorylation of myosin light chain. Taken together, these findings indicate that tangeretin, upon pre- or post-treatment, inhibits the SPC-induced CASM contraction through suppressing the Fyn/ROK signaling pathway, thereby suggesting that tangeretin can be a potential candidate for the treatment and/or prevention of vasospasm.
我们之前发现 SPC/Fyn/Rho-kinase(ROK)通路介导冠状动脉平滑肌(CASM)收缩的钙敏化,导致血管痉挛,这是猝死的主要原因。最近,我们一直在努力寻找和开发更多的天然食用化合物,以治疗和/或预防 SPC 诱导的异常 CASM 收缩,最终我们首次发现,从柑橘类植物中提取的天然化合物橘红素(5,6,7,8,4'-五甲氧基黄酮),可以抑制 SPC 诱导的 CASM 收缩,无论是预处理还是后处理。在猪 CASM 组织中,橘红素在最佳浓度下对 SPC 诱导的收缩具有显著的抑制作用,对 SPC 诱导的高 K 去极化诱导的 Ca 依赖性收缩也具有适度的抑制作用;在预处理和后处理时;关于机制,橘红素通过抑制 SPC 诱导的 Fyn 和 ROK 从细胞质向细胞膜的激活和易位,显著消除了 SPC 诱导的细胞收缩,导致肌球蛋白轻链的磷酸化减少。总之,这些发现表明,橘红素通过抑制 Fyn/ROK 信号通路,在预处理或后处理时抑制 SPC 诱导的 CASM 收缩,表明橘红素可以成为治疗和/或预防血管痉挛的潜在候选药物。