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Neuroscience ; 134(3): 1023-32, 2005.
Article in English | MEDLINE | ID: mdl-16039797

ABSTRACT

The mammalian RFamide-related peptide RFRP1 was found to signal through the neuropeptide FF 2 receptor expressed in Xenopus oocytes. The peptide induced a dose-dependent outward current, which was dependent on the simultaneous expression of GIRK1 and GIRK4 potassium channels. In neuropathic rats, RFRP1 administered intrathecally induced tactile antiallodynia and thermal antinociception, whereas in the solitary tract nucleus it produced only mechanical antihyperalgesia. Expression of the RFamide-related peptide mRNA in the rat CNS was distinctly different from that of neuropeptide FF. Most notably, the gene was not expressed in the hindbrain or spinal cord at detectable levels. However, there was a prominent group of RFamide-related peptide mRNA-expressing neurons in the central hypothalamus, in the area in and between the dorsomedial and ventromedial nuclei. The results suggest that RFamide-related peptides are potentially involved in pain regulation through a hypothalamo-medullary projection system, and possibly via action on neuropeptide FF 2 receptors. In neuropathic animals, the pain suppressive effect of RFamide-related peptide varies depending on the submodality of noxious test stimulation and the site of RFamide-related peptide administration.


Subject(s)
Neuropeptides/administration & dosage , Pain/drug therapy , Receptors, Neuropeptide/physiology , Signal Transduction/physiology , Animals , Cloning, Molecular/methods , Dose-Response Relationship, Drug , G Protein-Coupled Inwardly-Rectifying Potassium Channels , Humans , In Situ Hybridization/methods , Male , Membrane Potentials/drug effects , Membrane Potentials/physiology , Membrane Potentials/radiation effects , Microinjections/methods , Neuropeptides/pharmacology , Pain/physiopathology , Pain Measurement/methods , Pain Threshold/drug effects , Potassium Channels, Inwardly Rectifying/metabolism , RNA, Messenger/metabolism , Rats , Rats, Wistar , Reaction Time/drug effects , Solitary Nucleus/drug effects , Solitary Nucleus/physiopathology , Spinal Cord/drug effects , Spinal Cord/physiopathology , Xenopus laevis
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