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新型化合物NK1和NK2受体拮抗剂FK224对豚鼠体内由神经激肽和感觉神经刺激所诱导的气道收缩及气道水肿的影响。

Effects of FK224, a novel compound NK1 and NK2 receptor antagonist, on airway constriction and airway edema induced by neurokinins and sensory nerve stimulation in guinea pigs.

作者信息

Murai M, Morimoto H, Maeda Y, Kiyotoh S, Nishikawa M, Fujii T

机构信息

Department of Pharmacology, Fujisawa Pharmaceutical Co., Ltd., Osaka, Japan.

出版信息

J Pharmacol Exp Ther. 1992 Jul;262(1):403-8.

PMID:1378097
Abstract

FK224 (N-[N2-[N-[N-[N-[2,3-didehydro-N-methyl-N-[N-[3-(2- penthylphenyl)-propionyl]-L-threonyl]tyrosyl]-L-leucynyl]-D- phenylalanyl]-L-allo-threonyl]-L-asparaginyl]-L-serine-nu-lactone) is a novel neurokinin (NK) antagonist that exhibits selectivity for NK1 and NK2 receptors. The effects of FK224 on airway constriction and airway edema induced by NKs and nerve stimulation have been investigated in guinea pigs. FK224 inhibited the contraction of isolated guinea pig trachea induced by substance P (SP, 10(-8) M), NKA (10(-9) M) and NKB (10(-8) M) in a concentration-dependent manner, and the IC50 values were 2.6 x 10(-6), 1.3 x 10(-6) and 2.3 x 10(-7) M, respectively. Tracheal contraction induced by histamine and acetylcholine was not affected by FK224, suggesting a specific effect on NK-mediated responses. FK224 also inhibited the atropine-resistant contraction of isolated guinea pig bronchi induced by electrical field stimulation with an IC50 value of 3.5 x 10(-6) M. In in vivo experiments, FK224 given i.v. inhibited SP (13.5 micrograms kg-1)-, NKA (1.1 micrograms kg-1)- and capsaicin (3.1 micrograms kg-1)-induced airway constriction in guinea pigs with ED50 values of 0.39 mg kg-1, 0.36 mg kg-1 and 1.1 mg kg-1, respectively. FK224 also inhibited SP (1.3 micrograms kg-1)-, NKA (11 micrograms kg-1)- and capsaicin (100 micrograms kg-1)-induced airway edema with ED50 values of 0.14 mg kg-1, 0.29 mg kg-1 and 0.30 mg kg-1, respectively.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

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]酪氨酰基]-L-亮氨酰基]-D-苯丙氨酰基]-L-别苏氨酰基]-L-天冬氨酰基]-L-丝氨酸-γ-内酯)是一种新型神经激肽(NK)拮抗剂,对NK1和NK2受体具有选择性。在豚鼠中研究了FK224对NKs和神经刺激诱导的气道收缩和气道水肿的影响。FK224以浓度依赖性方式抑制由P物质(SP,10^(-8) M)、神经激肽A(NKA,10^(-9) M)和神经激肽B(NKB,10^(-8) M)诱导的离体豚鼠气管收缩,IC50值分别为2.6×10^(-6)、1.3×10^(-6)和2.3×10^(-7) M。组胺和乙酰胆碱诱导的气管收缩不受FK224影响,表明其对NK介导的反应具有特异性作用。FK224还抑制电场刺激诱导的离体豚鼠支气管的阿托品抗性收缩,IC50值为3.5×10^(-6) M。在体内实验中,静脉注射FK224可抑制豚鼠中SP(13.5微克/千克)、NKA(1.1微克/千克)和辣椒素(3.1微克/千克)诱导的气道收缩,ED50值分别为0.39毫克/千克、0.36毫克/千克和1.1毫克/千克。FK224还抑制SP(1.3微克/千克)、NKA(11微克/千克)和辣椒素(100微克/千克)诱导的气道水肿,ED50值分别为0.14毫克/千克、0.29毫克/千克和0.30毫克/千克。(摘要截断于250字)

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