Inhibitor Design for Monoamine Oxidases

被引:0
作者
Ramsay, Rona R. [1 ]
机构
[1] Univ St Andrews, St Andrews KY16 9ST, Fife, Scotland
关键词
Anti-depressant; monoamine oxidase; neurotransmitter levels; structure-based drug design; covalently-bound FAD; steady-state kinetic analysis; redox state; B-CATALYZED OXIDATION; METHYLENE-BLUE; ACTIVE-SITE; MAO-A; SPECIES-DIFFERENCES; LIGAND-BINDING; BENZYLAMINE ANALOGS; IMIDAZOLINE LIGANDS; SEROTONIN TOXICITY; AMINE OXIDASES;
D O I
暂无
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Flavin-containing monoamine oxidases (MAO A and MAO B) located on the outer membrane of mitochondria oxidise amines and generate hydrogen peroxide. Inhibitors alleviate depression by increasing neurotransmitter levels in the brain. Elevation of neurotransmitters, although an established outcome, is a delicate balance because complete lack of MAO A is associated with aggression and combination of monoamine oxidase inhibitors with reuptake inhibitors can result in serotonin toxicity. MAO in the periphery is essential for protection against biogenic amines, so inhibition there is an undesirable side effect both of antidepressants and drugs for other targets. MAO also metabolizes many amine drugs, an important factor in pharmacokinetics. This review summarises the structure, assay and regulation of MAO. The importance of reliable inhibition data properly analysed for these flavoenzymes is emphasised. It describes some current drugs and how new compounds that inhibit MAO are emerging from structure-based drug design.
引用
收藏
页码:2529 / 2539
页数:11
相关论文
共 143 条
  • [51] Interaction of psychotropic drugs with monoamine oxidase in rat brain
    Gnerre, C
    Kosel, M
    Baumann, P
    Carrupt, PA
    Testa, B
    [J]. JOURNAL OF PHARMACY AND PHARMACOLOGY, 2001, 53 (08) : 1125 - 1130
  • [52] New pyrazoline bearing 4(3H)-quinazolinone inhibitors of monoamine oxidase: Synthesis, biological evaluation, and structural determinants of MAO-A and MAO-B selectivity
    Goekhan-Kelekci, Nesrin
    Koyunoglu, Semra
    Yabanoglu, Samiye
    Yelekci, Kemal
    Oezgen, Oezen
    Ucar, Guelberk
    Erol, Kevser
    Kendi, Engin
    Yesilada, Akguel
    [J]. BIOORGANIC & MEDICINAL CHEMISTRY, 2009, 17 (02) : 675 - 689
  • [53] Groeger G, 2009, ANTIOXID REDOX SIGN, V11, P2655, DOI [10.1089/ars.2009.2728, 10.1089/ARS.2009.2728]
  • [54] Activated MAO-B in the brain of Alzheimer patients, demonstrated by [11C]-L-deprenyl using whole hemisphere autoradiography
    Gulyas, Balazs
    Pavlova, Elena
    Kasa, Peter
    Gulya, Karoly
    Bakota, Lidia
    Varszegi, Szilvia
    Keller, Eva
    Horvath, Monika Csilla
    Nag, Sangram
    Hermecz, Istvan
    Magyar, Kalman
    Halldin, Christer
    [J]. NEUROCHEMISTRY INTERNATIONAL, 2011, 58 (01) : 60 - 68
  • [55] HAEFELY W, 1993, CLIN NEUROPHARMACOL, V16, pS8
  • [56] Tyramine oxidase. I. A new enzyme system in liver.
    Hare, MLC
    [J]. BIOCHEMICAL JOURNAL, 1928, 22 (04) : 968 - 979
  • [57] Molecular docking of inhibitors into monoamine oxidase B
    Harkcom, William T.
    Bevan, David R.
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2007, 360 (02) : 401 - 406
  • [58] A peroxidase-coupled continuous absorbance plate-reader assay for flavin monoamine oxidases, copper-containing amine oxidases and related enzymes
    Holt, Andrew
    Palcic, Monica M.
    [J]. NATURE PROTOCOLS, 2006, 1 (05) : 2498 - 2505
  • [59] REACTION PATHWAY OF MEMBRANE-BOUND RAT-LIVER MITOCHONDRIAL MONOAMINE-OXIDASE
    HOUSLAY, MD
    TIPTON, KF
    [J]. BIOCHEMICAL JOURNAL, 1973, 135 (04) : 735 - 750
  • [60] Hubalek F, 2004, FASEB J, V18, pC191