Matthijs G, Peeters T L, Vantrappen G
Department of Medical Research, University of Leuven, Belgium.
Regul Pept. 1988 Jun;21(3-4):321-30. doi: 10.1016/0167-0115(88)90015-8.
Motilin and acetylcholine (ACh) have a direct contractile effect on rabbit small intestinal smooth muscle. To explore the role of calcium influx in these contractions, we studied the effect of extracellular calcium concentration and of calcium antagonists on the response of longitudinal muscle preparations from rabbit duodenum. Motilin- (10(-7) M) and ACh- (10(-4) M)-induced contractions were abolished in Ca2+-depleted medium. ACh (10(-4) M) or motilin (10(-8) and 10(-7) M) increased the contractile response to added Ca2+ to 130 +/- 6%, 129 +/- 10% and 145 +/- 5% of the maximal response to Ca2+ added alone (10 mM in a cumulative concentration response curve). The sensitivity to Ca2+ was greater in the presence of ACh and motilin (EC50 = 1.0 and 1.1 mM Ca2+) than in the absence of any agonist (1.7 mM). In cumulative concentration response (CCR) curves for motilin and ACh, pD2'-values were 7.0 and 6.6 for diltiazem, 8.4 and 7.8 for verapamil (two calcium entry blockers), 5.6 and 5.2 for TMB-8 (an inhibitor of intracellular calcium), 5.3 and 5.2 for TFP (a calmodulin-antagonist). All CCR-curves showed metactoid-like action of the antagonistic drugs. We conclude that ACh and motilin cause calcium to enter the smooth muscle cell. They are probably operating via separate channels, and use a mechanism which differs from K+-induced influx. Intracellular calcium stores appear to play a minor role in these contractions.
胃动素和乙酰胆碱(ACh)对兔小肠平滑肌有直接的收缩作用。为了探究钙内流在这些收缩中的作用,我们研究了细胞外钙浓度和钙拮抗剂对兔十二指肠纵行肌标本反应的影响。在无钙培养基中,胃动素(10⁻⁷ M)和乙酰胆碱(10⁻⁴ M)诱导的收缩被消除。乙酰胆碱(10⁻⁴ M)或胃动素(10⁻⁸和10⁻⁷ M)使对添加钙的收缩反应增加至单独添加钙(在累积浓度反应曲线中为10 mM)最大反应的130±6%、129±10%和145±5%。在存在乙酰胆碱和胃动素时对钙的敏感性(EC50 = 1.0和1.1 mM钙)高于无任何激动剂时(1.7 mM)。在胃动素和乙酰胆碱的累积浓度反应(CCR)曲线中,地尔硫䓬的pD2'值分别为7.0和6.6,维拉帕米(两种钙通道阻滞剂)为8.4和7.8,TMB - 8(细胞内钙抑制剂)为5.6和5.2,三氟拉嗪(钙调蛋白拮抗剂)为5.3和5.2。所有CCR曲线均显示拮抗药物呈类双曲线作用。我们得出结论,乙酰胆碱和胃动素使钙进入平滑肌细胞。它们可能通过不同的通道起作用,并且使用一种不同于钾离子诱导内流的机制。细胞内钙库在这些收缩中似乎起次要作用。