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雷马卡林对去甲肾上腺素诱导的兔肠系膜动脉Ca2+浓度变化及机械活动的影响。

Effects of lemakalim on changes in Ca2+ concentration and mechanical activity induced by noradrenaline in the rabbit mesenteric artery.

作者信息

Ito S, Kajikuri J, Itoh T, Kuriyama H

机构信息

Department of Pharmacology, Faculty of Medicine, Kyushu University, Fukuoka, Japan.

出版信息

Br J Pharmacol. 1991 Sep;104(1):227-33. doi: 10.1111/j.1476-5381.1991.tb12411.x.

Abstract
  1. Effects of (-)-cromakalim (lemakalim) on tension and Ca2+ mobilization induced by noradrenaline (NA) were investigated by measuring intracellular Ca2+ concentration ([Ca2+]i) isometric tension and production of inositol-1,4,5-trisphosphate (IP3) in smooth muscle strips of the rabbit mesenteric artery. 2. In thin smooth muscle strips, 10 microM NA produced a large phasic, followed by a small tonic increase in [Ca2+]i, which correlated well with the evoked phasic and tonic contractions, respectively. Lemakalim (0.1-10 microM) lowered the resting [Ca2+]i without a decrease in the resting tension, and also inhibited the increased [Ca2+]i and tension induced by 10 microM NA, all in a concentration-dependent manner. Glibenclamide (1 microM) inhibited these actions of lemakalim. 3. In Ca(2+)-free solution containing 2 mM EGTA, NA (10 microM) transiently increased [Ca2+]i, tension and synthesis of IP3. Lemakalim (over 0.01 microM) inhibited these actions of NA in Ca(2+)-free solution containing 5.9 mM K+, but not in Ca(2+)-free solution containing 128 mM K+. These actions of lemakalim were prevented by glibenclamide (1 microM). Lemakalim (1 microM) did not modify the increases in [Ca2+]i and tension induced by 10 mM caffeine. 4. In beta-escin-skinned strips, 10 microM NA increased [Ca2+]i in Ca(2+)-free solution containing 50 microM EGTA, 3 microM guanosine triphosphate (GTP) and 2 microM Fura 2 after the storage sites were loaded by application of 0.3 microM Ca2+ for 2 min, suggesting that Ca2+ is released from intracellular storage sites following activation of the alpha-adrenoceptor. Lemakalim (1 microM) did not inhibit the Ca2+ release from storage sites induced by NA. 5. We conclude that lemakalim inhibits NA-induced Ca2 + release due to inhibition of NA-induced 'P3 production in a manner dependent on the membrane potential and causes inhibition of the phasic contraction induced by NA.
摘要
  1. 通过测量兔肠系膜动脉平滑肌条中的细胞内钙离子浓度([Ca2+]i)、等长张力和肌醇-1,4,5-三磷酸(IP3)的产生,研究了(-)-克罗卡林(雷马卡林)对去甲肾上腺素(NA)诱导的张力和钙离子动员的影响。2. 在薄的平滑肌条中,10微摩尔/升的NA引起[Ca2+]i大幅的相位性升高,随后是小幅的持续性升高,这分别与诱发的相位性和持续性收缩密切相关。雷马卡林(0.1 - 10微摩尔/升)降低静息[Ca2+]i但不降低静息张力,并且也以浓度依赖的方式抑制10微摩尔/升NA诱导的[Ca2+]i升高和张力。格列本脲(1微摩尔/升)抑制雷马卡林的这些作用。3. 在含有2毫摩尔/升乙二醇双四乙酸(EGTA)的无钙溶液中,NA(10微摩尔/升)短暂升高[Ca2+]i、张力和IP3的合成。在含有5.9毫摩尔/升钾离子的无钙溶液中,雷马卡林(超过0.01微摩尔/升)抑制NA的这些作用,但在含有128毫摩尔/升钾离子的无钙溶液中则不然。雷马卡林的这些作用被格列本脲(1微摩尔/升)阻断。雷马卡林(1微摩尔/升)不改变10毫摩尔/升咖啡因诱导的[Ca2+]i和张力升高。4. 在经β-七叶皂苷处理使细胞膜通透的肌条中,在通过施加0.3微摩尔/升钙离子2分钟使储存位点加载后,10微摩尔/升的NA在含有50微摩尔/升EGTA、3微摩尔/升鸟苷三磷酸(GTP)和2微摩尔/升氟罗红2的无钙溶液中升高[Ca2+]i,这表明钙离子在α-肾上腺素受体激活后从细胞内储存位点释放。雷马卡林(1微摩尔/升)不抑制NA诱导的储存位点钙离子释放。5. 我们得出结论,雷马卡林以依赖膜电位的方式抑制NA诱导的IP3产生,从而抑制NA诱导的钙离子释放,并导致抑制NA诱导的相位性收缩。

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