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7-硝基吲唑及相关取代吲唑对大鼠小脑一氧化氮合酶的抑制作用。

Inhibition of rat cerebellar nitric oxide synthase by 7-nitro indazole and related substituted indazoles.

作者信息

Babbedge R C, Bland-Ward P A, Hart S L, Moore P K

机构信息

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

出版信息

Br J Pharmacol. 1993 Sep;110(1):225-8. doi: 10.1111/j.1476-5381.1993.tb13796.x.

Abstract
  1. 7-Nitro indazole (7-NI) produces potent inhibition of rat cerebellar nitric oxide synthase (NOS) with an IC50 of 0.9 +/- 0.1 microM (n = 6). NOS activity is dependent on the presence of both exogenous CaCl2 and NADPH. The inhibitory potency of 7-NI remained unaltered in the presence of different concentrations of either CaCl2 (0.75-7.5 mM) or NADPH (0.05-5.0 mM). 2. Kinetic (Lineweaver-Burke) analysis of the effect of 7-NI on rat cerebellar NOS revealed that inhibition was of a competitive nature with a Ki value of 5.6 microM. The Km of of cerebellar NOS with respect to L-arginine was 2.5 microM. 3. The following indazole derivatives (IC50 values shown in parentheses, all n = 6) caused concentration-related inhibition of rat cerebellar NOS in vitro: 6-nitro indazole (31.6 +/- 3.4 microM), 5-nitro indazole (47.3 +/- 2.3 microM), 3-chloro indazole (100.0 +/- 5.5 microM), 3-chloro 5-nitro indazole (158.4 +/- 2.1 microM) and indazole (177.8 +/- 2.1 microM). The IC50 values for 5-amino indazole, 6-amino indazole and 6-sulphanilimido indazole were in excess of 1 mM; 3-indazolinone was inactive. 4. 7-NI (10 mg kg-1) administered i.p. to rats produced 60 min thereafter a significant inhibition of NOS activity in cerebellum (31.1 +/- 3.2%, n = 6), cerebral cortex (38.2 +/- 5.6%, n = 6), hippocampus (37.0 +/- 2.8%, n = 6) and adrenal gland (23.7 +/- 3.0%, n = 6). NOS activity in olfactory bulb and stomach fundus were unchanged. 5. These results indicate that 7-NI is a potent and competitive inhibitor of rat brain NOS in vitro and also inhibits NOS in different brain regions and in the adrenal gland in vivo. Inhibition of NOS is a characteristic property of the indazole nucleus. Nitration of the indazole ring at positions 5, 6 and 7 results in a graded increase in inhibitory potency. Indazole-based inhibitors of NOS may prove useful tools with which to evaluate the biological roles of nitric oxide in the central nervous system.
摘要
  1. 7-硝基吲唑(7-NI)对大鼠小脑一氧化氮合酶(NOS)有强效抑制作用,半数抑制浓度(IC50)为0.9±0.1微摩尔/升(n = 6)。NOS活性依赖于外源性氯化钙(CaCl2)和烟酰胺腺嘌呤二核苷酸磷酸(NADPH)的存在。在不同浓度的CaCl2(0.75 - 7.5毫摩尔/升)或NADPH(0.05 - 5.0毫摩尔/升)存在时,7-NI的抑制效力保持不变。2. 对7-NI对大鼠小脑NOS作用的动力学(Lineweaver-Burke)分析表明,抑制作用具有竞争性,抑制常数(Ki)值为5.6微摩尔/升。小脑NOS对L-精氨酸的米氏常数(Km)为2.5微摩尔/升。3. 以下吲唑衍生物(括号内为IC50值,均n = 6)在体外对大鼠小脑NOS产生浓度相关的抑制作用:6-硝基吲唑(31.6±3.4微摩尔/升)、5-硝基吲唑(47.3±2.3微摩尔/升)、3-氯吲唑(100.0±5.5微摩尔/升)(158.4±2.1微摩尔/升)和吲唑(177.8±2.1微摩尔/升)。5-氨基吲唑、6-氨基吲唑和6-磺胺基吲唑的IC50值超过1毫摩尔/升;3-吲唑啉酮无活性。4. 给大鼠腹腔注射7-NI(10毫克/千克)后60分钟,小脑(31.1±3.2%,n = 6)、大脑皮层(38.2±5.6%,n = 6)、海马体(37.0±2.8%,n = 6)和肾上腺(23.7±3.0%,n = 6)中的NOS活性受到显著抑制。嗅球和胃底中的NOS活性未改变。5. 这些结果表明,7-NI在体外是大鼠脑NOS的强效竞争性抑制剂,在体内也能抑制不同脑区和肾上腺中的NOS。抑制NOS是吲唑核的一个特性。吲唑环在5、6和7位硝化会导致抑制效力分级增加。基于吲唑的NOS抑制剂可能是评估一氧化氮在中枢神经系统中生物学作用的有用工具。

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