Choi Seok, Choi Jeong June, Jun Jae Yeoul, Koh Jae Woong, Kim Sang Hun, Kim Dong Hee, Pyo Myoung-Yun, Choi Sangzin, Son Jin Pub, Lee Inki, Son Miwon, Jin Mirim
Department of Physiology, College of Medicine, Chosun University, Gwangju 501-759, Korea.
Mol Cells. 2009 Mar 31;27(3):307-12. doi: 10.1007/s10059-009-0039-6. Epub 2009 Mar 19.
The interstitial cells of Cajal (ICC) are pacemaking cells required for gastrointestinal motility. The possibility of whether DA-9701, a novel prokinetic agent formulated with Pharbitis Semen and Corydalis Tuber, modulates pacemaker activities in the ICC was tested using the whole cell patch clamp technique. DA-9701 produced membrane depolarization and increased tonic inward pacemaker currents in the voltage-clamp mode. The application of flufenamic acid, a non-selective cation channel blocker, but not niflumic acid, abolished the generation of pacemaker currents induced by DA-9701. Pretreatment with a Ca2+-free solution and thapsigargin, a Ca2+-ATPase inhibitor in the endoplasmic reticulum, abolished the generation of pacemaker currents. In addition, the tonic inward currents were inhibited by U-73122, an active phospholipase C inhibitor, but not by GDP-beta-S, which permanently binds G-binding proteins. Furthermore, the protein kinase C inhibitors, chelerythrine and calphostin C, did not block the DA-9701-induced pacemaker currents. These results suggest that DA-9701 might affect gastrointestinal motility by the modulation of pacemaker activity in the ICC, and the activation is associated with the non-selective cationic channels via external Ca2+ influx, phospholipase C activation, and Ca2+ release from internal storage in a G protein-independent and protein kinase C-independent manner.
Cajal间质细胞(ICC)是胃肠蠕动所需的起搏细胞。使用全细胞膜片钳技术测试了由牵牛子和延胡索制成的新型促动力剂DA-9701是否调节ICC中的起搏活动。在电压钳模式下,DA-9701引起膜去极化并增加内向性起搏电流。应用非选择性阳离子通道阻滞剂氟芬那酸而非尼氟酸可消除DA-9701诱导的起搏电流的产生。用无钙溶液和内质网中的Ca2 + -ATP酶抑制剂毒胡萝卜素预处理可消除起搏电流的产生。此外,内向性电流被活性磷脂酶C抑制剂U-73122抑制,但未被永久结合G蛋白的GDP-β-S抑制。此外,蛋白激酶C抑制剂白屈菜红碱和钙泊三醇C并未阻断DA-9701诱导的起搏电流。这些结果表明,DA-9701可能通过调节ICC中的起搏活动来影响胃肠蠕动,并且这种激活与非选择性阳离子通道相关,通过外部Ca2 +内流、磷脂酶C激活以及以G蛋白非依赖性和蛋白激酶C非依赖性方式从内部储存中释放Ca2 +。