Sung Tae Sik, Ko Seok Jae, Choi Woo-Gyun, Park Jae-Woo, Kim Byung Joo
Department of Physiology, Kosin University College of Medicine, Busan 49267, Republic of Korea.
Department of Clinical Korean Medicine, Graduate School of Kyung Hee University, Seoul 02447, Republic of Korea.
Int J Med Sci. 2025 Jul 24;22(13):3412-3421. doi: 10.7150/ijms.116169. eCollection 2025.
Koidzumi (AMK) is a traditional herbal medicine used for digestive disorders, yet its effects on colonic motility remain poorly understood. This study aimed to investigate the impact of AMK on human colonic contractility and pacemaker activity of interstitial cells of Cajal (ICCs), as well as its effect on intestinal transit. Human colonic tissues were obtained during non-obstructive colon surgery and used to assess spontaneous smooth muscle contractions and migrating motor complexes (MMCs). Electrophysiological recordings of pacemaker potentials were performed in murine colonic ICCs using whole-cell patch clamp. Pharmacological studies examined the involvement of ATP-sensitive K⁺ channels and cAMP signaling. The intestinal transit rate (ITR) was evaluated in a neostigmine-induced hypermotility mouse model. AMK treatment significantly reduced spontaneous contractions and MMCs in human colonic segments in a dose-dependent manner. In muine colonic ICCs, AMK suppressed pacemaker potentials, with an IC₅₀ of 37.89 µg/mL. This inhibitory effect was reversed by glibenclamide and 8-bromo-cAMP, suggesting involvement of ATP-sensitive K⁺ channels and cAMP-dependent pathways. , AMK attenuated neostigmine-induced increases in ITR. These findings highlight AMK's potential as a modulator of gastrointestinal motility.
小泉(AMK)是一种用于治疗消化系统疾病的传统草药,但其对结肠动力的影响仍知之甚少。本研究旨在探讨AMK对人结肠收缩性和 Cajal 间质细胞(ICC)起搏器活动的影响,以及其对肠道转运的作用。在非梗阻性结肠手术期间获取人结肠组织,用于评估自发性平滑肌收缩和移行运动复合波(MMC)。使用全细胞膜片钳在小鼠结肠 ICC 中进行起搏器电位的电生理记录。药理学研究检测了 ATP 敏感性钾通道和 cAMP 信号通路的参与情况。在新斯的明诱导的肠蠕动亢进小鼠模型中评估肠道转运率(ITR)。AMK 处理以剂量依赖性方式显著降低人结肠段的自发性收缩和 MMC。在小鼠结肠 ICC 中,AMK 抑制起搏器电位,IC₅₀ 为 37.89 µg/mL。格列本脲和 8-溴-cAMP 可逆转这种抑制作用,提示 ATP 敏感性钾通道和 cAMP 依赖性途径的参与。此外,AMK 减弱了新斯的明诱导的 ITR 增加。这些发现突出了 AMK 作为胃肠动力调节剂的潜力。