Wang Guo-Xiang, Xiang Yan-Li, Wang Hong-Gang, Miu Yang-de, Yu Guang
Department of Gastroenterology, Taizhou Municipal Hospital, Taizhou, Zhejiang, China 318000.
Gastroenterol Res Pract. 2020 Apr 3;2020:8610653. doi: 10.1155/2020/8610653. eCollection 2020.
Evodiamine (Evo) is an indole alkaloid extracted from the traditional Chinese medicinal herb . Evo may regulate gastrointestinal motility, but the evidence is insufficient, and the mechanisms remain unknown. The aim of this study was to investigate the effect of Evo on colonic motility of rats and the underlying mechanisms . Rat colonic muscle was exposed to Evo (10 and 100 M) followed by immunohistochemistry of cholecystokinin receptor 1 (CCK1R). Muscle contractions were studied in an organ bath system to determine whether CCK1R, nitric oxide (NO), and enteric neurons are involved in the relaxant effect of Evo. Whole-cell patch-clamp was used to detect L-type calcium currents ( ) in isolated colonic smooth muscle cells (SMCs). CCK1R was observed in SMCs, intermuscular neurons, and mucosa of rat colon. Evo could inhibit spontaneous muscle contractions; NO synthase, inhibitor L-NAME CCK1R antagonist, could partly block this effect, while the enteric neurons may not play a major role. Evo inhibited the peak in colonic SMCs at a membrane potential of 0 mV. The current-voltage (I-V) relationship of L-type calcium channels was modified by Evo, while the peak of the I-V curve remained at 0 mV. Furthermore, Evo inhibited the activation of L-type calcium channels and decreased the peak . The relaxant effect of Evo on colonic muscle is associated with the inhibition of L-type calcium channels. The enteric neurons, NO, and CCK1R may be partly related to the inhibitory effect of Evo on colonic motility. This study provides the first evidence that evodiamine can regulate colonic motility in rats by mediating calcium homeostasis in smooth muscle cells. These data form a theoretical basis for the clinical application of evodiamine for treatment of gastrointestinal motility diseases.
吴茱萸碱(Evo)是从传统中草药中提取的一种吲哚生物碱。Evo可能调节胃肠动力,但证据不足,其机制仍不清楚。本研究旨在探讨Evo对大鼠结肠动力的影响及其潜在机制。将大鼠结肠肌肉暴露于Evo(10和100μM),随后进行胆囊收缩素受体1(CCK1R)的免疫组织化学检测。在器官浴系统中研究肌肉收缩,以确定CCK1R、一氧化氮(NO)和肠神经元是否参与Evo的舒张作用。采用全细胞膜片钳技术检测分离的结肠平滑肌细胞(SMCs)中的L型钙电流( )。在大鼠结肠的SMC、肌间神经元和黏膜中观察到CCK1R。Evo可抑制肌肉自发收缩;NO合酶抑制剂L-NAME、CCK1R拮抗剂可部分阻断此效应,而肠神经元可能不起主要作用。Evo在膜电位为0 mV时抑制结肠SMC中的峰值 。Evo改变了L型钙通道的电流-电压(I-V)关系,而I-V曲线的峰值仍保持在0 mV。此外,Evo抑制L型钙通道的激活并降低峰值 。Evo对结肠肌肉的舒张作用与抑制L型钙通道有关。肠神经元、NO和CCK1R可能部分与Evo对结肠动力的抑制作用有关。本研究首次提供证据表明吴茱萸碱可通过介导平滑肌细胞内钙稳态来调节大鼠结肠动力。这些数据为吴茱萸碱治疗胃肠动力疾病的临床应用奠定了理论基础。