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Molecular Pain

, 1:33

First Online: 18 November 2005Received: 15 July 2005Accepted: 18 November 2005


BackgroundThe CO-NO-cGMP signalling system participates in the regulation of many physiological processes. The roles this system plays in spinal cord nociceptive signalling are particularly important. While individual components have been examined in isolation, little study has been dedicated to understanding the regulation and functioning of the system as a whole.

ResultsIn these studies we examined the time course of expression of 13 genes coding for components of this system including isoforms of the heme oxygenase HO, nitric oxide synthase NOS, soluble guanylate cyclase sGC, cGMP dependent protein kinase PKG and phosphodiesterase PDE enzyme systems. Of the 13 genes studied, 11 had spinal cord mRNA levels elevated at one or more time points up to 48 hours after hindpaw formalin injection. Of the 11 with elevated mRNA, 8 had elevated protein levels 48 hours after formalin injection when mechanical allodynia was maximal. No component had an increased protein level which did not have an increased mRNA level at one or more time points. Injection of morphine 10 mg-kg prior to formalin completely abolished the acute nociceptive behaviours, but did not alter the degree of sensitivity which developed in the formalin treated hind paws during the subsequent 48 hours. Morphine treatment did, however, eliminate formalin induced increases in enzyme protein levels.

ConclusionOur results indicate that the expression of the components of the CO-NO-cGMP signalling system seems to be coordinated in such a way that a generalized multi-level enhancement rather than a tightly limited step specific response occurs with noxious stimulation. Furthermore, the analgesic morphine administered prior to noxious stimulation can prevent long-term changes in gene expression though not necessarily nociceptive sensitisation.

Electronic supplementary materialThe online version of this article doi:10.1186-1744-8069-1-33 contains supplementary material, which is available to authorized users.

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Autor: Xiaoyou Shi - Xiangqi Li - J David Clark


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