ラット褐色細胞腫由来PC12培養細胞のニコチン性アセチルコリンレセプターチャネルに対するカルタップの作用

  • 永田 啓一
    Institute of Agriculture and Forestry, University of Tsukuba
  • 池田 朋子
    Institute of Agriculture and Forestry, University of Tsukuba
  • 青山 絵美
    Institute of Agriculture and Forestry, University of Tsukuba
  • 正野 俊夫
    Institute of Agriculture and Forestry, University of Tsukuba

書誌事項

タイトル別名
  • Cartap Modulation of the Nicotinic Acetylcholine Receptor-Channel of Clonal Rat Phaeochromocytoma (PC12) Cells
  • Cartap Modulation of the Nicotinic Acet

この論文をさがす

抄録

Cartap, the synthetic analog of nereistoxin, is known to act on the nicotinic acetylcholine receptorchannel (AChR). Effects of cartap on the neuronal nicotinic AChR of clonal rat phaeochromocytoma (PC12) cells were studied using a single-channel patch clamp method. When cartap was co-applied with acetylcholine, the single-channel openings were shortened and occurred in bursts separated by brief closures or gaps. The current amplitudes in the presence of cartap were virtually identical to those of currents induced by ACh only. Mean open time and burst duration were significantly decreased in the presence of cartap in a dose-dependent manner. These changes of single-channel kinetics result in a significant decrease in total charge carried through the open AChR explaining the suppressive effect of cartap on nicotinic AChR. Results suggest that cartap could act as an open channel blocker at the nicotinic AChR.

収録刊行物

被引用文献 (2)*注記

もっと見る

参考文献 (19)*注記

もっと見る

詳細情報 詳細情報について

問題の指摘

ページトップへ