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

被引:192
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
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