Ashoori F, Hidaka H, Tomita T
Br J Pharmacol. 1986 Jan;87(1):15-22. doi: 10.1111/j.1476-5381.1986.tb10151.x.
In the circular muscle of the fundic part of the guinea-pig stomach, a small tonic contraction could be repeatedly produced by carbachol in Ca-free solution containing 2 mM EGTA. The carbachol-induced response was gradually increased during prolonged exposure to Ca-free solution for 50 h, whereas a short treatment with 0.1-0.2 mM Ca suppressed the subsequent carbachol response in Ca-free solution. The response was not essentially modified by increasing the external K+ concentration to 40 mM. Calmodulin antagonists, N-(6-aminohexyl)-5-chloro-1-naphthalene sulphonamide (W-7) and trifluoperazine selectively suppressed the carbachol response in the presence of Ca (0.05 mM) and the contraction induced by Ca (0.1 mM), but they had little effect on the response to carbachol in Ca-free solution at a concentration of less than 10 microM. A vasodilator agent, N-(2-guanidinoethyl)-5-isoquinoline sulphonamide (HA-1004), inhibited the carbachol response both in the presence and absence of Ca, as well as the Ca-induced contraction, to a similar extent, provided that the external Ca concentration was less than 0.1 mM. These results led us to propose that the contraction evoked by carbachol in the absence of external Ca is mediated by a process independent of the Ca-calmodulin system.
在豚鼠胃底部的环形肌中,在含有2 mM乙二醇双四乙酸(EGTA)的无钙溶液中,卡巴胆碱可反复引发小幅度的强直性收缩。在无钙溶液中长时间暴露50小时期间,卡巴胆碱诱导的反应逐渐增强,而用0.1 - 0.2 mM钙进行短时间处理可抑制随后在无钙溶液中的卡巴胆碱反应。将细胞外钾离子浓度提高到40 mM对该反应基本无影响。钙调蛋白拮抗剂N -(6 - 氨基己基)- 5 - 氯 - 1 - 萘磺酰胺(W - 7)和三氟拉嗪在存在0.05 mM钙的情况下选择性抑制卡巴胆碱反应以及由0.1 mM钙诱导的收缩,但在浓度低于10 microM时,它们对无钙溶液中卡巴胆碱的反应影响很小。血管扩张剂N -(2 - 胍基乙基)- 5 - 异喹啉磺酰胺(HA - 1004)在有钙和无钙情况下均抑制卡巴胆碱反应以及钙诱导的收缩,且抑制程度相似,前提是细胞外钙浓度低于0.1 mM。这些结果使我们提出,在没有细胞外钙的情况下,卡巴胆碱诱发的收缩是由一个独立于钙 - 钙调蛋白系统的过程介导的。