Nitric oxide and carbon monoxide: parallel roles as neural messengers

被引:209
作者
Snyder, SH [1 ]
Jaffrey, SR [1 ]
Zakhary, R [1 ]
机构
[1] Johns Hopkins Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
关键词
heme; poly(ADP-ribose) polymerase; neurotoxicity; PDZ domain; protein kinase C; bilirubin;
D O I
10.1016/S0165-0173(97)00032-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Nitric oxide is now appreciated to be a molecule with important signaling functions in the body, The purification and cloning of the first NO synthesizing enzyme, NO synthase (NOS), from brain has led to the characterization of the roles of NO in normal physiology and in pathogenic states. NO synthesis is regulated in a complex manner, involving the association of activatory and inhibitory proteins. The body appears to use at least one other, highly related gas in a signaling function, carbon monoxide (CO). The enzyme responsible for CO biosynthesis in brain, heme oxygenase-2 (HO2), is rapidly regulated by neurotransmitter stimulation. The role for CO as neurotransmitter is suggested by the altered intestinal motility in mice harboring a genomic deletion of HO2. (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:167 / 175
页数:9
相关论文
共 67 条
[1]   PATHOLOGICAL IMPLICATIONS OF NITRIC-OXIDE, SUPEROXIDE AND PEROXYNITRITE FORMATION [J].
BECKMAN, JS ;
CROW, JP .
BIOCHEMICAL SOCIETY TRANSACTIONS, 1993, 21 (02) :330-334
[2]   SYMPOSIUM - CELLULAR-RESPONSE TO DNA DAMAGE - THE ROLE OF POLY(ADP-RIBOSE) - POLY(ADP-RIBOSE) IN THE CELLULAR-RESPONSE TO DNA DAMAGE [J].
BERGER, NA .
RADIATION RESEARCH, 1985, 101 (01) :4-15
[3]   BIOASSAY OF NITRIC-OXIDE RELEASED UPON STIMULATION OF NONADRENERGIC NONCHOLINERGIC NERVES IN THE CANINE ILEOCOLONIC JUNCTION [J].
BOECKXSTAENS, GE ;
PELCKMANS, PA ;
RUYTJENS, IF ;
BULT, H ;
DEMAN, JG ;
HERMAN, AG ;
VANMAERCKE, YM .
BRITISH JOURNAL OF PHARMACOLOGY, 1991, 103 (01) :1085-1091
[4]  
BREDT DS, 1992, J BIOL CHEM, V267, P10976
[5]   NITRIC-OXIDE MEDIATES GLUTAMATE-LINKED ENHANCEMENT OF CGMP LEVELS IN THE CEREBELLUM [J].
BREDT, DS ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (22) :9030-9033
[6]   LOCALIZATION OF NITRIC-OXIDE SYNTHASE INDICATING A NEURAL ROLE FOR NITRIC-OXIDE [J].
BREDT, DS ;
HWANG, PM ;
SNYDER, SH .
NATURE, 1990, 347 (6295) :768-770
[7]   ISOLATION OF NITRIC-OXIDE SYNTHETASE, A CALMODULIN-REQUIRING ENZYME [J].
BREDT, DS ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (02) :682-685
[8]   CLONED AND EXPRESSED NITRIC-OXIDE SYNTHASE STRUCTURALLY RESEMBLES CYTOCHROME-P-450 REDUCTASE [J].
BREDT, DS ;
HWANG, PM ;
GLATT, CE ;
LOWENSTEIN, C ;
REED, RR ;
SNYDER, SH .
NATURE, 1991, 351 (6329) :714-718
[9]   Interaction of nitric oxide synthase with the postsynaptic density protein PSD-95 and alpha 1-syntrophin mediated by PDZ domains [J].
Brenman, JE ;
Chao, DS ;
Gee, SH ;
McGee, AW ;
Craven, SE ;
Santillano, DR ;
Wu, ZQ ;
Huang, F ;
Xia, HH ;
Peters, MF ;
Froehner, SC ;
Bredt, DS .
CELL, 1996, 84 (05) :757-767
[10]   THE NEUROPROTECTIVE EFFECT OF A NITRIC-OXIDE INHIBITOR IN A RAT MODEL OF FOCAL CEREBRAL-ISCHEMIA [J].
BUISSON, A ;
PLOTKINE, M ;
BOULU, RG .
BRITISH JOURNAL OF PHARMACOLOGY, 1992, 106 (04) :766-767