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논문 기본 정보

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학술저널
저자정보
Seungheon Han (부산대학교) 김병주 (부산대학교) Bo Kyoung Jung (부산대학교) Song Ee Han (부산대학교) 남주현 (동국대학교) 권영규 (부산대학교) 나승열 (건국대학교) Jung Soo Kim (부산대학교)
저널정보
한국분자세포생물학회 Molecules and Cells Molecules and Cells 제33권 제3호
발행연도
2012.3
수록면
243 - 249 (7page)

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Ginsenoside, one of the active ingredients of Panax gin-seng, has a variety of physiological and pharmacological actions in various organs. However, little is known about the effects of ginsenosides on gastrointestinal (GI) motility. We studied the modulation of pacemaker potentials by ginsenoside in the interstitial cells of Cajal (ICCs) using the whole-cell patch clamp technique in the current clamp mode. Among ginsenosides, we investigated the effects of ginsenoside Rb1, Rg3 and Rf. While externally applied Rb1 and Rg3 had no effects on pacemaker potentials, Rf caused membrane depolarization. The application of flufenamic acid or niflumic acid abolished the generation of pacemaker potentials and inhibited the Rf-induced membrane depolarization. Membrane depolarization induced by Rf was not inhibited by intracellular application of guanosine 5?-[β-thio]diphosphate trilithium salt. Pre-treatment with a Ca2+-free solution, thapsigargin, a Ca2+-ATPase inhibitor of the endoplasmic reticulum, U-73122, a phospholipase C inhibitor, or 2-APB, an IP3 receptor inhibitor, abolished the generation of pacemaker potentials and suppressed Rf-induced actions. However, treatment with chelerythrine and calphostin C, protein kinase C inhibitors, did not block Rf-induced effects on pacemaker potentials. These results suggest that ginsenoside Rf modulates the pacemaker activities of ICCs and therby regulates intestinal motility.

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