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Nitric oxide (NO) serves as a retrograde messenger to activate neuronal NO synthase in the spinal cord via NMDA receptors
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DOI：10.1016/j.niox.2007.04.004.png)
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Abstract
En 中文
We have recently demonstrated that nitric oxide (NO) produced by neuronal NO synthase (nNOS) in the spinal cord is involved in the maintenance of neuropathic pain. To clarify whether NO itself affected nNOS activity in the spinal cord as a retrograde messenger, we examined the involvement of the NO/cGMP signaling pathway in the regulation of nNOS activity by NADPH-diaphorase histochemistry. NO-generating agents NOR3 (t(1/2) = 30 min) and SNAP (t(1/2) = 5 h), but not NORI (t(1/2) = 1.8 min), significantly enhanced NADPH-diaphorase staining in the spinal cord. 8-Br-cGMP also enhanced it similar to that by NOR3, and 8-Br-cAMP and forskolin, an activator of adenylate cyclase, enhanced it moderately. NOR I and NOR3 markedly increased the cGMP level in the spinal cord. The enhancement of NADPH-diaphorase staining by NOR3 was significantly inhibited by CPTIO, an NO scavenger, ODQ, a soluble guanylate cyclase inhibitor, and KT5823, an inhibitor of cGMP-dependent protein kinase. Additionally, the NOR3-enhanced nNOS activity was completely inhibited by NMDA antagonists MK-801 and D-AP5, partially by the GluR epsilon 2-selective antagonist CP-101,606, and was attenuated in GluR epsilon 1(-/-) and GluR epsilon 1(-/-)/epsilon 4(-/-) mice. These results suggest that NO may regulate nNOS activity as a retrograde messenger in the spinal cord via activation of NMDA receptor containing GluR epsilon 1 and GluR epsilon 2 subunits. (c) 2007 Elsevier Inc. All rights reserved.
Keywords:
nitric oxide (NO)
neuronal nitric oxide synthase (nNOS)
NO donor
NADPH diaphorase
NMDA receptors
spinal cord
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