Please use this identifier to cite or link to this item: https://doi.org/10.1186/1744-8069-9-37
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dc.titleInhibition of endogenous NGF degradation induces mechanical allodynia and thermal hyperalgesia in rats
dc.contributor.authorOsikowicz, M
dc.contributor.authorLongo, G
dc.contributor.authorAllard, S
dc.contributor.authorCuello, A.C
dc.contributor.authorRibeiro-da-Silva, A
dc.date.accessioned2020-10-28T07:19:58Z
dc.date.available2020-10-28T07:19:58Z
dc.date.issued2013
dc.identifier.citationOsikowicz, M, Longo, G, Allard, S, Cuello, A.C, Ribeiro-da-Silva, A (2013). Inhibition of endogenous NGF degradation induces mechanical allodynia and thermal hyperalgesia in rats. Molecular Pain 9 (1) : 37. ScholarBank@NUS Repository. https://doi.org/10.1186/1744-8069-9-37
dc.identifier.issn1744-8069
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/181807
dc.description.abstractBackground: We have previously shown a sprouting of sympathetic fibers into the upper dermis of the skin following subcutaneous injection of complete Freund's adjuvant (CFA) into the hindpaw. This sprouting correlated with an increase in pain-related sensitivity. We hypothesized that this sprouting and pain-related behavior were caused by an increase in nerve growth factor (NGF) levels. In this study, we investigated whether the inhibition of mature NGF degradation, using a matrix metalloproteinase 2 and 9 (MMP-2/9) inhibitor, was sufficient to reproduce a similar phenotype.Results: Behavioral tests performed on male Sprague-Dawley rats at 1, 3, 7 and 14 days after intra-plantar MMP-2/9 inhibitor administration demonstrated that acute and chronic injections of the MMP-2/9 inhibitor induced sensitization, in a dose dependent manner, to mechanical, hot and cold stimuli as measured by von Frey filaments, Hargreaves and acetone tests, respectively. Moreover, the protein levels of mature NGF (mNGF) were increased, whereas the levels and enzymatic activity of matrix metalloproteinase 9 were reduced in the glabrous skin of the hind paw. MMP-2/9 inhibition also led to a robust sprouting of sympathetic fibers into the upper dermis but there were no changes in the density of peptidergic nociceptive afferents.Conclusions: These findings indicate that localized MMP-2/9 inhibition provokes a pattern of sensitization and fiber sprouting comparable to that previously obtained following CFA injection. Accordingly, the modulation of endogenous NGF levels should be considered as a potential therapeutic target for the management of inflammatory pain associated with arthritis. © 2013 Osikowicz et al.; licensee BioMed Central Ltd.
dc.rightsAttribution 4.0 International
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.sourceUnpaywall 20201031
dc.subjectacetone
dc.subjectgelatinase A
dc.subjectgelatinase B
dc.subjectnerve growth factor
dc.subjectenzyme inhibitor
dc.subjectgelatinase A
dc.subjectgelatinase B
dc.subjectnerve growth factor
dc.subjectallodynia
dc.subjectanimal behavior
dc.subjectanimal experiment
dc.subjectanimal model
dc.subjectarticle
dc.subjectautonomic innervation
dc.subjectcontrolled study
dc.subjectdermis
dc.subjectenzyme activity
dc.subjectenzyme inhibition
dc.subjectglabrous skin
dc.subjecthyperalgesia
dc.subjecthypersensitivity
dc.subjectinflammatory pain
dc.subjectmale
dc.subjectnerve sprouting
dc.subjectnociception
dc.subjectnociceptive stimulation
dc.subjectnonhuman
dc.subjectpain threshold
dc.subjectpriority journal
dc.subjectprotein degradation
dc.subjectprotein localization
dc.subjectprotein targeting
dc.subjectrat
dc.subjectsensitization
dc.subjectsensory analysis
dc.subjectsensory nerve
dc.subjectskin nerve
dc.subjectsympathetic nerve
dc.subjectanimal
dc.subjectdrug effects
dc.subjecthyperalgesia
dc.subjectmetabolism
dc.subjectskin
dc.subjectSprague Dawley rat
dc.subjectAnimals
dc.subjectEnzyme Inhibitors
dc.subjectHyperalgesia
dc.subjectMale
dc.subjectMatrix Metalloproteinase 2
dc.subjectMatrix Metalloproteinase 9
dc.subjectNerve Growth Factor
dc.subjectRats
dc.subjectRats, Sprague-Dawley
dc.subjectSkin
dc.typeArticle
dc.contributor.departmentPHARMACOLOGY
dc.description.doi10.1186/1744-8069-9-37
dc.description.sourcetitleMolecular Pain
dc.description.volume9
dc.description.issue1
dc.description.page37
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