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Effects of Prunus mume Siebold & Zucc. in the pacemaking activity of interstitial cells of Cajal in murine small intestine

机译:梅苏·塞布尔德和Zucc的影响。 在鼠小肠中Cajal间质细胞的起轴活动中

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Interstitial cells of Cajal (ICCs) function as pacemaker cells in the gastrointestinal (GI) tract and therefore, serve an important role in regulating GI motility. The effects of a species of plum (Prunus mume Siebold & Zucc.) on cultured ICC cluster-induced pacemaker potentials in the mouse small intestine were investigated, and the effects of a methanolic extract of Prunus mume (m-PM) on ICC pacemaker activities were examined using the whole-cell patch-clamp technique. ICC pacemaker membrane potentials were depolarized by m-PM in a concentration dependent manner in current clamp mode. 4-Diphenylacetoxy-N-methyl-piperidine methiodide, which is a muscarinic 3 (M-3) receptor antagonist, was able to block m-PM-induced pacemaker potential increases, whereas methoctramine, which is a muscarinic 2 (M-2) receptor antagonist, was not. When 1 mM guanosine diphosphate (3-5 was present in the pipette solution, m-PM induced slight pacemaker depolarization. Following pretreatment in bath solution of Ca2+-free solution or a Ca'+-ATPase inhibitor in endoplasmic reticulum, the pacemaker currents were inhibited. Furthermore, pretreatment with PD98059, SB203580 or SP600125, which is a c-jun NH2-terminal kinase inhibitor, blocked m-PM-induced ICC potential depolarization. Furthermore, m-PM inhibited transient receptor potential melastatin (TRPM) 7 channels, but did not affect Ca2+-activated Cl- channels. These results suggest that m-PM is able to modulate pacemaker potentials through the muscarinic M-3 receptor, via G-protein and external and internal Ca2+, in a mitogen-activated protein kinase and TRPM7-dependent manner. Therefore, m-PM may provide a basis for the development of a novel gastroprokinetic agent.
机译:Cajal(ICCs)的间质细胞(ICCs)用作胃肠道(GI)的起搏器细胞,因此在调节GI运动中发挥重要作用。李子(Prunus Mume Siebold&Zuccc.)对小鼠小肠中培养的ICC簇诱导的起搏器电位的影响,以及蛋白驼粉(MP)对ICC起搏器活动的影响使用全细胞贴片技术检查。 ICC起搏器膜电位通过M-PM以浓度依赖性方式在电流钳位模式下被解耦。 4-二苯基乙酰氧基-N-甲基 - 哌啶甲基哌啶甲基碘化物,即肌肉蛋白3(M-3)受体拮抗剂,能够阻断MP-PM诱导的起搏器电位,而甲基氨基胺,这是一种毒蕈碱2(M-2)受体拮抗剂,不是。当1mM鸟氨酸二磷酸二磷酸(吸管溶液中3-5时,M-PM诱导轻微的起搏器去极化。在Ca2 + -Free溶液的预处理之后,在内质网的Ca2 + -Free溶液或Ca'+ - AtP酶抑制剂中,起搏器电流是抑制。此外,与PD98059,SB203580或SP600125的预处理是C-JUM NH2-末端激酶抑制剂,阻断了MP-PM诱导的ICC电位去极化。此外,M-PM抑制的瞬时受体潜在的旋转素(TRPM)7声道,但不影响CA2 + -Activated Cl-通道。这些结果表明M-PM能够在丝裂剂活化的蛋白激酶和外部和内部Ca2 +中通过毒蕈碱M-3受体调节起搏器电位TRPM7依赖性方式。因此,M-PM可以为新型胃陷性药剂的发展提供基础。

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