Sotníková R
Institute of Experimental Pharmacology, Slovak Academy of Sciences, Bratislava, CSFR.
Methods Find Exp Clin Pharmacol. 1992 Apr;14(3):175-81.
The effect of a new carbanilate derivative BK 129, 1-methoxymethyl-2(1-perhydroazepinyl)ethyl ester 2-(n)-pentyloxycarbanilic acid hydrochloride, was tested on preparations of canine dorsal pedal and coronary artery in vitro. The drug produced relaxation of arterial rings both under resting conditions and under precontraction with KCl. BK 129, at a concentration of 10(-5) mol/l, produced a shift to the right of the concentration-response curve of phenylephrine, with a decrease in the slope and a depression of the maximal response. BK 129 inhibited the response to norepinephrine and blocked histamine- and norepinephrine-induced contractions in Ca(2+)-free physiological salt solution. The electrical stimulation-induced contractions of arterial preparation were also inhibited. BK 129 shifted the concentration-response curve of CaCl2 in Ca(2+)-free depolarizing solution to the right in a non-competitive manner. It may be concluded that BK 129 is a local anesthetic which possesses relaxant properties. It appears to inhibit Ca2+ entry into the smooth muscle cell and Ca2+ release from sarcoplasmic reticulum.
一种新型氨基甲酸酯衍生物BK 129,即2-(n)-戊氧基氨基甲酸-1-甲氧基甲基-2-(1-全氢氮杂环庚烷基)乙酯盐酸盐,在犬离体背侧足背动脉和冠状动脉制剂上进行了测试。该药物在静息条件下以及在氯化钾预收缩后均能使动脉环舒张。浓度为10(-5)mol/l的BK 129使去氧肾上腺素的浓度-反应曲线右移,斜率降低,最大反应受到抑制。BK 129抑制对去甲肾上腺素的反应,并在无钙生理盐溶液中阻断组胺和去甲肾上腺素诱导的收缩。动脉制剂的电刺激诱导收缩也受到抑制。BK 129在无钙去极化溶液中以非竞争性方式使氯化钙的浓度-反应曲线右移。可以得出结论,BK 129是一种具有舒张特性的局部麻醉药。它似乎能抑制钙离子进入平滑肌细胞以及从肌浆网释放钙离子。