Rikkunshito Depolarizes Pacemaker Potentials of Cultured Interstitial Cells of Cajal through Ghrelin Receptors in Murine Small Intestine

被引:2
作者
Kim, Jeong Nam [1 ]
Nam, Joo Hyun [2 ]
Lee, Jong Rok [3 ]
Kim, Sang Chan [4 ]
Kwon, Young Kyu [1 ]
Kim, Byung Joo [1 ]
机构
[1] Pusan Natl Univ, Div Longev & Biofunct Med, Sch Korean Med, 49 Busandaehakro, Yangsan 50612, Gyeongsangnamdo, South Korea
[2] Dongguk Univ, Coll Med, Dept Physiol, Kyungju, South Korea
[3] Daegu Haany Univ, Dept Pharmaceut Engn, Gyongsan, South Korea
[4] Daegu Haany Univ, Coll Oriental Med, Gyongsan, South Korea
基金
新加坡国家研究基金会;
关键词
Rikkunshito; Interstitial cells of Cajal; Pacemaker potentials; Gastrointestinal tract; Motility; JUN-ZI-TANG; TRADITIONAL JAPANESE MEDICINE; SLOW-WAVE CURRENTS; HERBAL MEDICINE; KAMPO MEDICINE; NITRIC-OXIDE; SYMPTOMS; CHANNELS; INVOLVEMENT; RELAXATION;
D O I
10.1159/000498986
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Rikkunshito has been used to treat gastrointestinal (GI) disorders. The purpose of this study was to investigate the effects of Rikkunshito, a traditional Japanese herbal medicine, on the pacemaker potentials of interstitial cells of Cajal (ICCs) from the small intestines of mice.degrees Methods: We isolated ICCs from the small intestines of mice, and the whole-cell patch-clamp configuration was used to record the pacemaker potentials in cultured ICCs and membrane currents. Results: Rikkunshito depolarized ICC pacemaker potentials in a dose-dependent manner. Pretreatment with GSK1614343 or (D-Lys3)-growth hormone-releasing peptide-6 inhibited Rikkunshito-induced depolarization of pacemaker potentials. Intracellular GDP-beta-S inhibited Rikkunshito-induced effects. In Ca2+-free solution or in the presence of thapsigargin, Rikkunshito did not depolarize pacemaker potentials. Moreover, in the presence of U-73122 or xestospongin C, Rikkunshito-induced effects were inhibited. However, in the presence of staurosporine, Go6976 or Rottlerin, Rikkunshito depolarized pacemaker potentials. Furthermore, Rikkunshito inhibited both transient receptor potentials melastatin 7 (TRPM7) and Ca2+-activated Cl- channels (ANO1) currents. Conclusion: Rikkunshito depolarized pacemaker potentials of ICCs via ghrelin receptor and G protein through internal or external Ca2+-, phospholipase C-, and inositol triphosphate-dependent and protein kinase C-, TRPM7-, and ANO1-independent pathways. The study shows that Rikkunshito may alleviate GI motility disorders through its depolarizing effects on ICCs.
引用
收藏
页码:227 / 238
页数:12
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