Neuronal nitric oxide synthase: Structure, subcellular localization, regulation, and clinical implications

被引:511
作者
Zhou, Li [1 ]
Zhu, Dong-Ya [1 ]
机构
[1] Nanjing Med Univ, Dept Pharmacol, Sch Pharm, Nanjing 210029, Peoples R China
来源
NITRIC OXIDE-BIOLOGY AND CHEMISTRY | 2009年 / 20卷 / 04期
关键词
nNOS; Nitric oxide; Neurogenesis; Excitotoxicity; PDZ domain; Depression; Alzheimer's disease; Learning and memory; Parkinson's disease; IMPAIRED COGNITIVE PERFORMANCE; NO COMPLEX-FORMATION; D-ASPARTATE RECEPTOR; ALZHEIMERS-DISEASE; ELECTRON-TRANSFER; SKELETAL-MUSCLE; HIPPOCAMPAL NEUROGENESIS; CELL-DEATH; SYNAPTIC PLASTICITY; SUBVENTRICULAR ZONE;
D O I
10.1016/j.niox.2009.03.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Nitric oxide (NO), a free gaseous signaling molecule, is involved in the regulation of the cardiovascular, nervous and immune system. The neurotransmitter function of nitric oxide is dependent on dynamic regulation of its biosynthetic enzyme, nitric oxide synthase (NOS). There are three types of NOS, neuronal nitric oxide synthase (nNOS), endothelial nitric oxide synthase (eNOS) and inducible nitric oxide synthase (iNOS). Of the three NOS, we focus on nNOS in the present review. Brain nNOS exists in particulate and soluble forms and the differential subcellular localization of nNOS may contribute to its diverse functions. Proteins bearing PDZ domains can interact directly with the PDZ domain of nNOS, influencing the subcellular distribution and/or activity of the enzyme. During the past several years, an increasing number of reports have demonstrated the importance of nNOS in a variety of synaptic signaling events. nNOS has been implicated in modulating physiological functions such as learning, memory, and neurogenesis, as well as being involved in a number of human diseases. In this review we concentrate on recent findings regarding the structural features, subcellular localization and factors regulating nNOS function. In particular, we conclude with a section discussing the role of nNOS in a wide range of physiological and pathological conditions. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:223 / 230
页数:8
相关论文
共 125 条
[1]   Protection by cholesterol-extracting cyclodextrins:: a role for N-methyl-D-aspartate receptor redistribution [J].
Abulrob, A ;
Tauskela, JS ;
Mealing, G ;
Brunette, E ;
Faid, K ;
Stanimirovic, D .
JOURNAL OF NEUROCHEMISTRY, 2005, 92 (06) :1477-1486
[2]   Neuronal nitric-oxide synthase mutant (Ser-1412 → Asp) demonstrates surprising connections between heme reduction, NO complex formation, and catalysis [J].
Adak, S ;
Santolini, J ;
Tikunova, S ;
Wang, Q ;
Johnson, JD ;
Stuehr, DJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (02) :1244-1252
[3]   7-Nitroindazole, a neuronal nitric oxide synthase inhibitor, impairs passive-avoidance and elevated plus-maze memory performance in rats [J].
Akar, Furuzan Yildiz ;
Ulak, Guner ;
Tanyeri, Pelin ;
Erden, Faruk ;
Utkan, Tijen ;
Gacar, Nejat .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2007, 87 (04) :434-443
[4]   Differential effects of serotonin reuptake inhibitors on erectile responses, NO-production, and neuronal NO synthase expression in rat corpus cavernosum tissue [J].
Angulo, J ;
Peiró, C ;
Sanchez-Ferrer, CF ;
Gabancho, S ;
Cuevas, P ;
Gupta, S ;
de Tejada, IS .
BRITISH JOURNAL OF PHARMACOLOGY, 2001, 134 (06) :1190-1194
[5]   Molecular mechanisms of calcium-dependent neurodegeneration in excitotoxicity [J].
Arundine, M ;
Tymianski, M .
CELL CALCIUM, 2003, 34 (4-5) :325-337
[6]  
BANNERMAN DM, 1994, J NEUROSCI, V14, P7404
[7]   Neuronal nitric-oxide synthase is regulated by the hsp90-based chaperone system in vivo [J].
Bender, AT ;
Silverstein, AM ;
Demady, DR ;
Kanelakis, KC ;
Noguchi, S ;
Pratt, WB ;
Osawa, Y .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (03) :1472-1478
[8]   Species, strain and developmental variations in hippocampal neuronal and endothelial nitric oxide synthase clarify discrepancies in nitric oxide-dependent synaptic plasticity [J].
Blackshaw, S ;
Eliasson, MJL ;
Sawa, A ;
Watkins, CC ;
Krug, D ;
Gupta, A ;
Arai, T ;
Ferrante, RJ ;
Snyder, SH .
NEUROSCIENCE, 2003, 119 (04) :979-990
[9]   ALTERED SYNAPTIC PLASTICITY AND MEMORY FORMATION IN NITRIC-OXIDE SYNTHASE INHIBITOR-TREATED RATS [J].
BOHME, GA ;
BON, C ;
LEMAIRE, M ;
REIBAUD, M ;
PIOT, O ;
STUTZMANN, JM ;
DOBLE, A ;
BLANCHARD, JC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (19) :9191-9194
[10]   Neuronal-type NO synthase:: Transcript diversity and expressional regulation [J].
Boissel, JP ;
Schwarz, PM ;
Förstermann, U .
NITRIC OXIDE-BIOLOGY AND CHEMISTRY, 1998, 2 (05) :337-349