RGD Reference Report - Thrombin inhibits NMDA-mediated nociceptive activity in the mouse: possible mediation by endothelin. - Rat Genome Database

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Thrombin inhibits NMDA-mediated nociceptive activity in the mouse: possible mediation by endothelin.

Authors: Fang, M  Kovacs, KJ  Fisher, LL  Larson, AA 
Citation: Fang M, etal., J Physiol. 2003 Jun 15;549(Pt 3):903-17. Epub 2003 Apr 25.
RGD ID: 7387270
Pubmed: PMID:12717003   (View Abstract at PubMed)
PMCID: PMC2342990   (View Article at PubMed Central)
DOI: DOI:10.1113/jphysiol.2002.036384   (Journal Full-text)

The CNS expresses many components of an extracellular protease signalling system, including the protease-activated receptor-1 (PAR-1) whose tethered ligand is generated by thrombin. Activation of PAR-1 potentiates NMDA receptor activity in hippocampal neurons. Because NMDA activity mediates hyperalgesia, we tested the hypothesis that PAR-1 receptors also regulate pain processing. In contrast to the potentiating effect of thrombin in the hippocampus, NMDA-induced behaviours and the transient mechanical hyperalgesia (von Frey fibres) induced by intrathecally injected NMDA in mice were inhibited by thrombin in a dose-related fashion. This anti-hyperalgesic effect was mimicked by SFLLRN, the natural ligand at PAR-1 binding sites, but not SLIGRL-amide, a PAR-2 agonist. The effects of SFLLRN were less potent and shorter in duration than that of thrombin, consistent with its more transient effect on PAR-1 sites. Both thrombin and SFLLRN inhibited acetic acid-induced abdominal stretch (writhing) behaviours, which were also sensitive to NMDA antagonism, but not hot plate or tail flick latencies, which were insensitive to NMDA antagonists. TFLLR-amide, a selective ligand for PAR-1 sites, mimicked the effects of thrombin while RLLFT-amide, an inactive, reverse peptide sequence, did not. In addition, the effect of TFLLR-amide was prevented by RWJ-56110, a PAR-1 antagonist. Thrombin and TFLLR-amide produced no oedema (Evans Blue extravasation) in the spinal cord that would account for these effects. Based on the reported ability of thrombin to mobilize endothelin-1 from astrocytes, we tested the role of this compound in thrombin's activity. BQ123, an endothelin A receptor antagonist, prevented thrombin's inhibition of writhing and NMDA-induced behaviours while BQ788, an endothelin B receptor antagonist, did not. Thus, activation of PAR-1 sites by thrombin in the CNS appears to inhibit NMDA-mediated nociception by a pathway involving endothelin type A receptors.



RGD Manual Disease Annotations    Click to see Annotation Detail View

  
Object SymbolSpeciesTermQualifierEvidenceWithNotesSourceOriginal Reference(s)
F2RHumanHyperalgesia  ISOF2r (Mus musculus) RGD 
F2rRatHyperalgesia  ISOF2r (Mus musculus) RGD 
F2rMouseHyperalgesia  IDA  RGD 

Objects Annotated

Genes (Rattus norvegicus)
F2r  (coagulation factor II (thrombin) receptor)

Genes (Mus musculus)
F2r  (coagulation factor II thrombin receptor)

Genes (Homo sapiens)
F2R  (coagulation factor II thrombin receptor)


Additional Information