Please use this identifier to cite or link to this item: https://doi.org/10.1016/S0304-3959(01)00491-2
DC FieldValue
dc.titleIncreased synaptosomal [3H] GABA uptake in the rat brainstem after facial carrageenan injections
dc.contributor.authorNg, C.-H.
dc.contributor.authorOng, W.-Y.
dc.date.accessioned2015-09-09T07:03:27Z
dc.date.available2015-09-09T07:03:27Z
dc.date.issued2002
dc.identifier.citationNg, C.-H., Ong, W.-Y. (2002). Increased synaptosomal [3H] GABA uptake in the rat brainstem after facial carrageenan injections. Pain 98 (3) : 259-268. ScholarBank@NUS Repository. https://doi.org/10.1016/S0304-3959(01)00491-2
dc.identifier.issn03043959
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/120752
dc.description.abstractThe aim of the present study was to quantify synaptosomal [3H] gamma aminobutyric acid (GABA) uptake in the rat brainstem after facial carrageenan injections. Synaptosomal preparations from the brainstem of rats that had received one or four facial carrageenan injections showed greater GABA binding on the side of the brainstem ipsilateral to the carrageenan injection than on the contralateral side when compared to saline injected controls. In contrast, no difference in GABA binding between the injected and contralateral sides was observed in the same synaptosomal preparations that had been treated with GABA uptake inhibitors NNC-711, β-alanine, or nipecotic acid. The difference between GABA binding in the absence of the GABA uptake inhibitor and GABA binding in a portion from the same synaptosomal preparation which had been incubated with the GABA uptake inhibitor was obtained to represent [3H] GABA binding to GABA transporters/transporter mediated [3H] GABA uptake. A significantly greater GABA uptake was observed on the side of the brainstem ipsilateral to the carrageenan injection(s) than on the contralateral side. A consequence of the observed increase in GABA uptake is that it could reduce the amount of GABA in the synaptic cleft. This could influence the transmission of nociceptive input from primary afferents to secondary neurons in the spinal trigeminal nucleus and could be a contributing factor in the development of hyperalgesia after carrageenan injections or other chronic inflammatory conditions. © 2002 International Association for the Study of Pain. Published by Elsevier Science B.V. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/S0304-3959(01)00491-2
dc.sourceScopus
dc.subjectChronic inflammation
dc.subjectGamma aminobutyric acid transporter
dc.subjectHyperalgesia
dc.subjectNociception
dc.subjectSpinal trigeminal nucleus
dc.subjectTrigeminal neuralgia
dc.typeArticle
dc.contributor.departmentANATOMY
dc.description.doi10.1016/S0304-3959(01)00491-2
dc.description.sourcetitlePain
dc.description.volume98
dc.description.issue3
dc.description.page259-268
dc.description.codenPAIND
dc.identifier.isiut000177317700004
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