Haruno A, Yamasaki Y, Miyoshi K, Miyake H, Tsuchiya K, Kosaka M, Nagai M, Iriki M
Biol. Res. Lab. Taiho Pharm. Co., Ltd, Tokushima, Japan.
Nihon Yakurigaku Zasshi. 1989 Aug;94(2):145-50. doi: 10.1254/fpj.94.145.
The effects of P-4 and its active metabolites in human blood and urine and the effects of 1-methyl-4-piperidyl diphenylpropoxyacetate N-oxide [P-4(N----O)], 1-methyl-4-piperidyl benzilate N-oxide [DPr-P-4(N----O)] and 1-methyl-4-piperidyl benzilate (DPr-P-4) on isolated guinea pig urinary bladder were investigated. At doses of 10(-6) or 10(-5) M, P-4 shifted the dose-response curve for acetylcholine (ACh) to the right, and at a dose of 10(-5) M, it also inhibited the maximum response of ACh. At doses of 10(-5) M or more, P-4(N----O) inhibited the maximum response of ACh. DPr-P-4(N----O) or DPr-P-4 shifted the dose-response curve for ACh to the right at doses of 10(-6)-10(-4) M or at doses of 10(-7)-10(-5) M. P-4 at doses of 10(-6) M or more inhibited the KCl (100 mM)-induced contraction in a dose-dependent manner, and its potency was quite equal to that of terodiline. The inhibitory effect of P-4(N----O), DPr-P-4(N----O) and DPr-P-4 in the KCl (100 mM)-induced contraction were weaker than that of P-4. P-4 and P-4(N----O) had a dose-dependent inhibitory effect on K+-induced 45Ca influx in isolated guinea-pig urinary bladder.(ABSTRACT TRUNCATED AT 250 WORDS)
研究了P - 4及其活性代谢产物在人血液和尿液中的作用,以及1 - 甲基 - 4 - 哌啶基二苯丙氧基乙酸N - 氧化物[P - 4(N→O)]、1 - 甲基 - 4 - 哌啶基二苯羟乙酸N - 氧化物[DPr - P - 4(N→O)]和1 - 甲基 - 4 - 哌啶基二苯羟乙酸(DPr - P - 4)对离体豚鼠膀胱的作用。在10(-6)或10(-5)M的剂量下,P - 4使乙酰胆碱(ACh)的剂量 - 反应曲线右移,在10(-5)M的剂量下,它还抑制了ACh的最大反应。在10(-5)M或更高剂量下,P - 4(N→O)抑制了ACh的最大反应。DPr - P - 4(N→O)或DPr - P - 4在10(-6) - 10(-4)M的剂量下或在10(-7) - 10(-5)M的剂量下使ACh的剂量 - 反应曲线右移。10(-6)M或更高剂量的P - 4以剂量依赖性方式抑制KCl(100 mM)诱导的收缩,其效力与特罗地林相当。P - 4(N→O)、DPr - P - 4(N→O)和DPr - P - 4在KCl(100 mM)诱导的收缩中的抑制作用比P - 4弱。P - 4和P - 4(N→O)对离体豚鼠膀胱中K + 诱导的45Ca内流具有剂量依赖性抑制作用。(摘要截短于250字)