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关于对肠道平滑肌起搏细胞的胆碱能和血清素能调节对起搏电位的影响的研究。

A Study on the Effects of Muscarinic and Serotonergic Regulation by on the Pacemaker Potential of the Interstitial Cells of Cajal in the Murine Small Intestine.

机构信息

Division of Longevity and Biofunctional Medicine, Pusan National University School of Korean Medicine, Yangsan 50612, Republic of Korea.

Department of Clinical Korean Medicine, Graduate School of Kyung Hee University, Seoul 02447, Republic of Korea.

出版信息

Int J Med Sci. 2023 May 21;20(8):1000-1008. doi: 10.7150/ijms.83986. eCollection 2023.

Abstract

In traditional Korean medicine, the 16-herb concoction (BGT) is used to treat various gastrointestinal (GI) diseases. In this study, we investigated the regulatory mechanism underlying the influence of BGT on the interstitial cells of Cajal (ICCs), pacemaker cells in the GI tract. Within 12 h of culturing ICCs in the small intestines of mice, the pacemaker potential of ICCs was recorded through an electrophysiological method. An increase in the BGT concentration induced depolarization and decreased firing frequency. This reaction was suppressed by cholinergic receptor muscarinic 3 (CHRM3) antagonists, as well as 5-hydroxytryptamine receptor (5HTR) 3 and 4 antagonists. Nonselective cation channel inhibitors, such as thapsigargin and flufenamic acid, along with protein kinase C (PKC) and mitogen-activated protein kinase (MAPK) inhibitors, also suppressed the BGT reaction. Guanylate cyclase and protein kinase G (PKG) antagonists inhibited BGT, but adenylate cyclase and protein kinase A antagonists had no effect. In conclusion, we demonstrated that BGT acts through CHRM3, 5HTR3, and 5HTR4 to regulate intracellular Ca concentrations and the PKC, MAPK, guanylate cycle, and PKG signaling pathways.

摘要

在传统的韩国医学中,十六味草药配方(BGT)被用于治疗各种胃肠道(GI)疾病。在这项研究中,我们研究了 BGT 对胃肠道起搏细胞——间质细胞 Cajal(ICCs)的影响的调节机制。通过电生理方法在培养的来自于小鼠小肠的 ICCs 中记录起搏电位。通过增加 BGT 浓度诱导去极化和降低放电频率来诱导 ICCs 起搏。这种反应被胆碱能受体毒蕈碱 3(CHRM3)拮抗剂、5-羟色胺受体(5HTR)3 和 4 拮抗剂以及非选择性阳离子通道抑制剂如 thapsigargin 和 flufenamic acid 抑制。蛋白激酶 C(PKC)和丝裂原激活蛋白激酶(MAPK)抑制剂也抑制 BGT 反应。鸟苷酸环化酶和蛋白激酶 G(PKG)拮抗剂抑制 BGT,但环腺苷酸酶和蛋白激酶 A 拮抗剂没有作用。总之,我们证明 BGT 通过 CHRM3、5HTR3 和 5HTR4 作用,调节细胞内 Ca 浓度以及 PKC、MAPK、鸟苷酸环化酶和 PKG 信号通路。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6820/10357445/3678ace17e75/ijmsv20p1000g001.jpg

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