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7-硝基吲唑,一种一氧化氮合酶抑制剂,在小鼠中表现出抗伤害感受活性且不升高血压。

7-Nitro indazole, an inhibitor of nitric oxide synthase, exhibits anti-nociceptive activity in the mouse without increasing blood pressure.

作者信息

Moore P K, Babbedge R C, Wallace P, Gaffen Z A, Hart S L

机构信息

Biomedical Sciences Division, King's College, University of London.

出版信息

Br J Pharmacol. 1993 Feb;108(2):296-7. doi: 10.1111/j.1476-5381.1993.tb12798.x.

Abstract

7-Nitro indazole (7-NI) inhibits mouse cerebellar nitric oxide synthase (NOS) in vitro with an IC50 of 0.47 microM. Following i.p. administration in mice, 7-NI (10-50 mg kg-1) produces dose-related anti-nociception as evidenced by an inhibition of late phase (15-30 min) but not early phase (0-5 min) hindpaw licking time following subplantar injection of formalin (10 microliters, 5% v/v). The ED50 for this effect was 26 mg kg-1 (equivalent to 159.5 mumol kg-1). Similar i.p. administration of 7-NI (20 and 80 mg kg-1) in urethane-anaesthetized mice failed to increase MAP. Thus, 7-NI is a novel inhibitor of NOS which exhibits selectivity for the brain enzyme. Accordingly, 7-NI may be a useful starting point for the development of selective, centrally acting NOS inhibitors devoid of cardiovascular side effects and as a tool to study the central pharmacological effects of nitric oxide (NO).

摘要

7-硝基吲唑(7-NI)在体外对小鼠小脑一氧化氮合酶(NOS)具有抑制作用,其半数抑制浓度(IC50)为0.47微摩尔。给小鼠腹腔注射后,7-NI(10 - 50毫克/千克)产生剂量相关的抗伤害感受作用,这可通过在足底注射福尔马林(10微升,5%体积/体积)后对后期(15 - 30分钟)而非早期(0 - 5分钟)后爪舔舐时间的抑制来证明。此效应的半数有效剂量(ED50)为26毫克/千克(相当于159.5微摩尔/千克)。在氨基甲酸乙酯麻醉的小鼠中腹腔注射类似剂量的7-NI(20和80毫克/千克)未能升高平均动脉压(MAP)。因此,7-NI是一种新型的NOS抑制剂,对脑型酶具有选择性。相应地,7-NI可能是开发无心血管副作用的选择性中枢作用NOS抑制剂的有用起点,并且可作为研究一氧化氮(NO)中枢药理作用的工具。

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