Targeted gene deletion of heme oxygenase 2 reveals neural role for carbon monoxide

被引:193
作者
Zakhary, R
Poss, KD
Jaffrey, SR
Ferris, CD
Tonegawa, S
Snyder, SH
机构
[1] Johns Hopkins Univ, Sch Med, Dept Neurosci, Baltimore, MD 21205 USA
[2] MIT, Ctr Canc Res, Howard Hughes Med Inst, Ctr Learning & Memory, Cambridge, MA 02139 USA
[3] MIT, Dept Biol, Cambridge, MA 02139 USA
[4] Johns Hopkins Univ, Sch Med, Div Gastroenterol, Baltimore, MD 21205 USA
[5] Johns Hopkins Univ, Sch Med, Div Pharmacol & Mol Sci, Baltimore, MD 21205 USA
[6] Johns Hopkins Univ, Sch Med, Div Psychiat & Behav Sci, Baltimore, MD 21205 USA
关键词
D O I
10.1073/pnas.94.26.14848
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Neuronal nitric oxide synthase (nNOS) generates NO in neurons, and heme-oxygenase-2 (HO-2) synthesizes carbon monoxide (GO). We have evaluated the roles of NO and CO in intestinal neurotransmission using mice with targeted deletions of nNOS or HO-2, Immunohistochemical analysis demonstrated colocalization of nNOS and HO-2 in myenteric ganglia, Nonadrenergic noncholinergic relaxation and cyclic guanosine 3',5' monophosphate elevations evoked by electrical field stimulation were diminished markedly in both nNOS(Delta/Delta) and HO-2(Delta/Delta) mice, In wild-type mice, NOS inhibitors and HO inhibitors partially inhibited nonadrenergic noncholinergic relaxation. In nNOS(Delta/Delta) animals, NOS inhibitors selectively lost their efficacy, and HO inhibitors were inactive in HO-2(Delta/Delta) animals.
引用
收藏
页码:14848 / 14853
页数:6
相关论文
共 42 条
[1]  
[Anonymous], 1988, Antibodies: A Laboratory Manual
[2]  
BANNERMAN DM, 1994, J NEUROSCI, V14, P7415
[3]  
BANNERMAN DM, 1994, J NEUROSCI, V14, P7404
[4]   TRANSMISSION FROM INTRAMURAL INHIBITORY NERVES TO SMOOTH MUSCLE OF GUINEA-PIG TAENIA COLI [J].
BENNETT, MR ;
BURNSTOCK, G ;
HOLMAN, ME .
JOURNAL OF PHYSIOLOGY-LONDON, 1966, 182 (03) :541-+
[5]   NONADRENERGIC NONCHOLINERGIC RELAXATION MEDIATED BY NITRIC-OXIDE IN THE CANINE ILEOCOLONIC JUNCTION [J].
BOECKXSTAENS, GE ;
PELCKMANS, PA ;
BULT, H ;
DEMAN, JG ;
HERMAN, AG ;
VANMAERCKE, YM .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1990, 190 (1-2) :239-246
[6]   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
[7]   POSSIBLE INVOLVEMENT OF NITRIC-OXIDE IN LONG-TERM POTENTIATION [J].
BOHME, GA ;
BON, C ;
STUTZMANN, JM ;
DOBLE, A ;
BLANCHARD, JC .
EUROPEAN JOURNAL OF PHARMACOLOGY, 1991, 199 (03) :379-381
[8]   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
[9]   NITRIC-OXIDE AS AN INHIBITORY NONADRENERGIC NONCHOLINERGIC NEUROTRANSMITTER [J].
BULT, H ;
BOECKXSTAENS, GE ;
PELCKMANS, PA ;
JORDAENS, FH ;
VANMAERCKE, YM ;
HERMAN, AG .
NATURE, 1990, 345 (6273) :346-347
[10]   HYDROGEN-PEROXIDE ELICITS PULMONARY ARTERIAL RELAXATION AND GUANYLATE-CYCLASE ACTIVATION [J].
BURKE, TM ;
WOLIN, MS .
AMERICAN JOURNAL OF PHYSIOLOGY, 1987, 252 (04) :H721-H732