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

Neuronal nitric oxide synthase (nNOS) generates NO in neurons, and heme-oxygenase-2 (HO-2) synthesizes carbon monoxide (CO). 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[prime],5[prime] monophosphate elevations evoked by electrical field stimulation were diminished markedly in both nNO[S.sup.[Delta]/[Delta]] and H[O-2.sup.[Delta]/[Delta]] mice. In wild-type mice, NOS inhibitors and HO inhibitors partially inhibited nonadrenergic noncholinergic relaxation. In nNO[S.sup.[Delta]/[Delta]] animals, NOS inhibitors selectively lost their efficacy, and HO inhibitors were inactive in H[O-2.sup.[Delta]/[Delta]] animals.