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Effects of ATP on Pacemaker Activity of Interstitial Cells of Cajal from the Mouse Small Intestine

机译:ATP对小鼠小肠Cajal间质细胞起搏器活性的影响

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摘要

Purinergic receptors play an important role in regulating gastrointestinal (GI) motility. Interstitial cells of Cajal (ICCs) are pacemaker cells that regulate GI smooth muscle activity. We studied the functional roles of external adenosine 5′-triphosphate (ATP) on pacemaker activity in cultured ICCs from mouse small intestines by using the whole-cell patch clamp technique and intracellular Ca2+ ([Ca2+]i) imaging. External ATP dose-dependently depolarized the resting membrane and produced tonic inward pacemaker currents, and these effects were antagonized by suramin, a purinergic P2 receptor antagonist. ATP-induced effects on pacemaker currents were suppressed by an external Na+-free solution and inhibited by the nonselective cation channel blockers, flufenamic acid and niflumic acid. The removal of external Ca2+ or treatment with thapsigargin (inhibitor of Ca2+ uptake into endoplasmic reticulum) inhibited the ATP-induced effects on pacemaker currents. Spontaneous [Ca2+]i oscillations were enhanced by external ATP. These results suggest that external ATP modulates pacemaker activity by activating nonselective cation channels via external Ca2+ influx and [Ca2+]i release from the endoplasmic reticulum. Thus, it seems that activating the purinergic P2 receptor may modulate GI motility by acting on ICCs in the small intestine.
机译:嘌呤能受体在调节胃肠(GI)运动中起重要作用。 Cajal间质细胞(ICC)是起搏器细胞,可调节GI平滑肌活动。我们使用全细胞膜片钳技术和细胞内Ca 2 + ([Ca < sup> 2 + ] i)成像。外部ATP剂量依赖性地使静息膜去极化,并产生强直性起搏器内向电流,这些作用被嘌呤能P2受体拮抗剂苏拉明所拮抗。 ATP对起搏器电流的影响被无Na + 的外部溶液抑制,而被非选择性阳离子通道阻滞剂,氟苯那酸和尼氟酸抑制。去除外部Ca 2 + 或用thapsigargin(Ca 2 + 内质网摄取抑制剂)处理抑制ATP诱导的起搏电流。自发的[Ca 2 + ] i振荡被外部ATP增强。这些结果表明,外部ATP通过激活外部Ca 2 + 内流和从内质网释放[Ca 2 + ] i的非选择性阳离子通道来调节起搏器活性。因此,似乎激活嘌呤能P2受体可以通过作用于小肠中的ICC来调节GI运动。

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