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Inhibition of peripheral nociceptors by aminoglycosides produces analgesia in inflammatory pain models in the rat
dc.creator | Mercado, Francisco | |
dc.creator | Almanza, Angélica | |
dc.creator | Simón-Arceo, Karina | |
dc.creator | López, Omar | |
dc.creator | Vega, Rosario | |
dc.creator | Coffeen, Ulises | |
dc.creator | Contreras, Bernardo | |
dc.creator | Soto, Enrique | |
dc.creator | Pellicer Francisco | |
dc.date.accessioned | 2017-06-29T03:53:48Z | |
dc.date.available | 2017-06-29T03:53:48Z | |
dc.date.issued | 2015 | es_ES |
dc.identifier | 2766 | es_ES |
dc.identifier.issn | 0360-3997 | es_ES |
dc.identifier.uri | http://repositorio.inprf.gob.mx/handle/123456789/4615 | |
dc.identifier.uri | https://doi.org/10.1007/s10753-014-9972-4 | es_ES |
dc.description.abstract | es_ES | |
dc.language.iso | eng | es_ES |
dc.publisher | New York, NY : Kluwer Academic/Plenum Publishers | es_ES |
dc.relation | 38 (2) 649-657 p. | es_ES |
dc.relation | versión del editor | es_ES |
dc.rights | acceso cerrado | es_ES |
dc.subject.mesh | Aminoglycosides-Pharmacology | es_ES |
dc.subject.mesh | Aminoglycosides-Therapeutic use | es_ES |
dc.subject.mesh | Analgesia-Methods | es_ES |
dc.subject.mesh | Animals | es_ES |
dc.subject.mesh | Disease Models, Animal | es_ES |
dc.subject.mesh | Inflammation-Drug therapy | es_ES |
dc.subject.mesh | Inflammation-Pathology | es_ES |
dc.subject.mesh | Male | es_ES |
dc.subject.mesh | Nociceptors-Drug effects | es_ES |
dc.subject.mesh | Nociceptors-Pathology | es_ES |
dc.subject.mesh | Pain-Drug therapy | es_ES |
dc.subject.mesh | Pain-Pathology | es_ES |
dc.subject.mesh | Pain Measurement-Drug effects | es_ES |
dc.subject.mesh | Pain Measurement-Methods | es_ES |
dc.subject.mesh | Rats | es_ES |
dc.subject.mesh | Rats, Wistar | es_ES |
dc.title | Inhibition of peripheral nociceptors by aminoglycosides produces analgesia in inflammatory pain models in the rat | es_ES |
dc.title.alternative | es_ES | |
dc.type | artículo | es_ES |
dc.contributor.affiliation | Laboratorio de Neurofisiología Integrativa, Dirección de Investigaciones en Neurociencias, Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz, Calz. México-Xochimilco 101. Col. San Lorenzo Huipulco, Del. Tlalpan, México, D.F., México, C.P. 14370 | es_ES |
dc.contributor.email | pellicer@imp.edu.mx | es_ES |
dc.relation.jnabreviado | INFLAMMATION | es_ES |
dc.relation.journal | Inflammation | es_ES |
dc.identifier.place | Estados Unidos | es_ES |
dc.date.published | 2015 | es_ES |
dc.identifier.organizacion | Instituto Nacional de Psiquiatría Ramón de la Fuente Muñiz | es_ES |
dc.identifier.eissn | 1573-2576 | es_ES |
dc.identifier.doi | 10.1007/s10753-014-9972-4 | es_ES |
dc.description.month | Abr | es_ES |
dc.description.abstractotrodioma | Aminoglycosides (AGs) modulate nociceptors and ionic channels expressed in sensory neurons. The AG applied in situ could be useful to alleviate hyperalgesia in animal models of inflammatory pain. We tested streptomycin (ST) and neomycin (NEO) as analgesic agents applied in situ in rat paw inflammation caused by formalin or carrageenan administration. The action of ST and NEO on the action potential discharge produced by acidic stimuli in isolated dorsal root ganglion neurons was also studied in current-clamp recordings. In the formalin test, ST and NEO significantly reduced the nociceptive behaviour. ST reduced the N-(4-methyl-2-quinazolinyl)-guanidine (GMQ)-induced nociceptive behaviour, and NEO diminished the hyperalgesia to thermonociception and mechanonociception produced by CAR. In the current-clamp experiments, ST and NEO reduced the generation of action potentials when an acidic solution was applied. We conclude that ST and NEO produce analgesia to inflammatory pain, an effect that is due in part to the inhibition of ASIC activation in sensory neurons | es_ES |
dc.subject.meshm | es_ES | |
dc.subject.kw | es_ES | |
dc.subject.ko | Aminoglycosides | es_ES |
dc.subject.ko | Nociception | es_ES |
dc.subject.ko | Inflammation | es_ES |
dc.subject.ko | ASICs | es_ES |
dc.subject.ko | Analgesia | es_ES |
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