苍术通过ICCs起搏器抑制和cAMP/ atp敏感的K +通道通路调节人结肠运动。

IF 3.2 3区 医学 Q1 MEDICINE, GENERAL & INTERNAL
International Journal of Medical Sciences Pub Date : 2025-07-24 eCollection Date: 2025-01-01 DOI:10.7150/ijms.116169
Tae Sik Sung, Seok Jae Ko, Woo-Gyun Choi, Jae-Woo Park, Byung Joo Kim
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引用次数: 0

摘要

苍术是一种用于治疗消化系统疾病的传统草药,但其对结肠运动的影响尚不清楚。本研究旨在探讨AMK对人结肠收缩力和Cajal间质细胞(ICCs)起搏器活性的影响,以及其在体内对肠道转运的影响。在非阻塞性结肠手术中获得人类结肠组织,并用于评估自发平滑肌收缩和迁移运动复合体(MMCs)。采用全细胞膜片钳对小鼠结肠icc的起搏器电位进行电生理记录。药理学研究检查了atp敏感的K +通道和cAMP信号的参与。在新斯的明诱导的小鼠运动亢进模型中评估肠转运率(ITR)。AMK治疗以剂量依赖的方式显著减少了人类结肠段的自发收缩和mmc。在小鼠结肠icc中,AMK抑制起搏器电位,IC₅0为37.89µg/mL。格列本脲和8-溴- camp逆转了这种抑制作用,这表明atp敏感的K +通道和camp依赖途径参与其中。在体内,AMK可减弱新斯的明诱导的ITR升高。这些发现突出了AMK作为胃肠运动调节剂的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

<i>Atractylodes macrocephala</i> Koidzumi modulates human colonic motility via ICCs pacemaker suppression and cAMP/ATP-sensitive K⁺ channel pathways.

<i>Atractylodes macrocephala</i> Koidzumi modulates human colonic motility via ICCs pacemaker suppression and cAMP/ATP-sensitive K⁺ channel pathways.

<i>Atractylodes macrocephala</i> Koidzumi modulates human colonic motility via ICCs pacemaker suppression and cAMP/ATP-sensitive K⁺ channel pathways.

Atractylodes macrocephala Koidzumi modulates human colonic motility via ICCs pacemaker suppression and cAMP/ATP-sensitive K⁺ channel pathways.

Atractylodes macrocephala 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 in vivo 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. In vivo, AMK attenuated neostigmine-induced increases in ITR. These findings highlight AMK's potential as a modulator of gastrointestinal motility.

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来源期刊
International Journal of Medical Sciences
International Journal of Medical Sciences MEDICINE, GENERAL & INTERNAL-
CiteScore
7.20
自引率
0.00%
发文量
185
审稿时长
2.7 months
期刊介绍: Original research papers, reviews, and short research communications in any medical related area can be submitted to the Journal on the understanding that the work has not been published previously in whole or part and is not under consideration for publication elsewhere. Manuscripts in basic science and clinical medicine are both considered. There is no restriction on the length of research papers and reviews, although authors are encouraged to be concise. Short research communication is limited to be under 2500 words.
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