Blocking NO synthesis: How, where and why?

被引:285
作者
Vallance, P [1 ]
Leiper, J [1 ]
机构
[1] UCL, Dept Med, BHF Labs, Ctr Clin Pharmacol, London WC1E 6JJ, England
基金
英国惠康基金;
关键词
D O I
10.1038/nrd960
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Nitric oxide (NO) is a key physiological mediator, and the association of disordered NO generation with many pathological conditions has led to much interest in pharmacologically modulating NO levels. However, the wide range of processes in which NO has been implicated, and the fact that increases or decreases in NO levels might be therapeutically desirable depending on the condition or even at different stages of the same condition, pose considerable challenges for drug development. Here, we focus on the rationale and potential for approaches that reduce NO synthesis, which have led to the development of several compounds that will shortly be entering clinical trials.
引用
收藏
页码:939 / 950
页数:12
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共 124 条
  • [1] Reduction in asymmetrical dimethylarginine, an endogenous nitric oxide synthase inhibitor, in the cerebrospinal fluid during aging and in patients with Alzheimer's disease
    Abe, T
    Tohgi, H
    Murata, T
    Isobe, C
    Sato, C
    [J]. NEUROSCIENCE LETTERS, 2001, 312 (03) : 177 - 179
  • [2] Nitric oxide synthases: structure, function and inhibition
    Alderton, WK
    Cooper, CE
    Knowles, RG
    [J]. BIOCHEMICAL JOURNAL, 2001, 357 (03) : 593 - 615
  • [3] Nitric oxide is proangiogenic in the retina and choroid
    Ando, A
    Yang, A
    Mori, K
    Yamada, H
    Yamada, E
    Takahashi, K
    Saikia, J
    Kim, M
    Melia, M
    Fishman, M
    Huang, P
    Campochiaro, PA
    [J]. JOURNAL OF CELLULAR PHYSIOLOGY, 2002, 191 (01) : 116 - 124
  • [4] Compartmentalised inducible nitric-oxide synthase activity in septic shock
    Annane, D
    Sanquer, S
    Sébille, V
    Faye, A
    Djuranovic, D
    Raphaël, JC
    Gajdos, P
    Bellissant, E
    [J]. LANCET, 2000, 355 (9210) : 1143 - 1148
  • [5] The protective role of nitric oxide in a neurotoxicant-induced demyelinating model
    Arnett, HA
    Hellendall, RP
    Matsushima, GK
    Suzuki, K
    Laubach, VE
    Sherman, P
    Ting, JPY
    [J]. JOURNAL OF IMMUNOLOGY, 2002, 168 (01) : 427 - 433
  • [6] Effect of inhibition of nitric oxide synthase on chronic tension-type headache: a randomised crossover trial
    Ashina, M
    Lassen, LH
    Bendtsen, L
    Jensen, R
    Olesen, J
    [J]. LANCET, 1999, 353 (9149) : 287 - 289
  • [7] N5-(1-imino-5-butenyl)-L-ornithine -: A neuronal isoform selective mechanism-based inactivator of nitric oxide synthase
    Babu, BR
    Griffith, OW
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (15) : 8882 - 8889
  • [8] Neural roles for heme oxygenase:: Contrasts to nitric oxide synthase
    Barañano, DE
    Snyder, SH
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2001, 98 (20) : 10996 - 11002
  • [9] Nitric oxide regulates the heart by spatial confinement of nitric oxide synthase isoforms
    Barouch, LA
    Harrison, RW
    Skaf, MW
    Rosas, GO
    Cappola, TP
    Kobeissi, ZA
    Hobai, IA
    Lemmon, CA
    Burnett, AL
    O'Rourke, B
    Rodriguez, ER
    Huang, PL
    Lima, JAC
    Berkowitz, DE
    Hare, JM
    [J]. NATURE, 2002, 416 (6878) : 337 - 340
  • [10] 3,4-dihydro-1-isoquinolinamines: A novel class of nitric oxide synthase inhibitors with a range of isoform selectivity and potency
    Beaton, H
    Hamley, P
    Nicholls, DJ
    Tinker, AC
    Wallace, AV
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY LETTERS, 2001, 11 (08) : 1023 - 1026