Shioya T, Kagaya M, Sano M, Itaba M, Shindo T, Fujii T, Miura M
Second Department of Internal Medicine, Akita University School of Medicine, Japan.
Arzneimittelforschung. 1995 Nov;45(11):1194-7.
The effect of FK224 (N-(N2-[N-¿N-(N-2,3-didehydro-N-methyl-N-[N-3- (2-pentylphenyl)-propionyl¿-L-threonyl]tyrosyl-L-leucynyl)-D -phenylalanyl¿-L-allothreonyl]-L-asparaginyl)-L-serine-v-lacto ne, CAS 125787-94-2) on isometric contraction of canine tracheal smooth muscle in situ was studied. Contraction was induced by administration of substance P, neurokinin A, and neurokinin B intra-arterially into the tracheal circulation in five mongrel dogs. FK224 inhibited substance P- and neurokinin A-induced contraction in a dose-dependent manner, but it did not inhibit neurokinin B-induced contraction significantly. These data suggest that FK224 is a dual antagonist of both neurokinin 1 and neurokinin 2 receptors, with a similar potency in in vivo experiments.
研究了FK224(N-(N2-[N-¿N-(N-2,3-二脱氢-N-甲基-N-[N-3-(2-戊基苯基)-丙酰基¿-L-苏氨酰基]酪氨酰-L-亮氨酰基)-D-苯丙氨酰基¿-L-别苏氨酰基]-L-天冬酰胺基)-L-丝氨酸-γ-内酯,CAS 125787-94-2)对犬原位气管平滑肌等长收缩的影响。在五只杂种犬中,通过向气管循环动脉内注射P物质、神经激肽A和神经激肽B诱导收缩。FK224以剂量依赖性方式抑制P物质和神经激肽A诱导的收缩,但对神经激肽B诱导的收缩无明显抑制作用。这些数据表明,FK224是神经激肽1和神经激肽2受体的双重拮抗剂,在体内实验中具有相似的效力。