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RESEARCH PRODUCT
Acetylsalicylic acid reduces heat responses in rat nociceptive primary sensory neurons – evidence for a new mechanism of action
Timo KirschsteinRolf-detlef TreedeHermann NawrathWolfgang Greffrathsubject
MaleHot TemperaturePatch-Clamp TechniquesPainchemistry.chemical_elementCalciumPharmacologyIon ChannelsMembrane PotentialsRats Sprague-Dawleychemistry.chemical_compoundDorsal root ganglionGanglia SpinalmedicineAnimalsCyclooxygenase InhibitorsThermosensingCalcium SignalingNeurons AfferentPatch clampCells CulturedAspirinDose-Response Relationship DrugGeneral NeuroscienceNociceptorsMicrofluorimetryElectric StimulationSensory neuronRatsmedicine.anatomical_structurechemistryMechanism of actionBiochemistryCapsaicinNociceptorCalciumCapsaicinmedicine.symptomSignal Transductiondescription
Acetylsalicylic acid (ASA) is thought to exert its peripheral analgesic effects via inhibition of cyclooxygenase. We now studied the effects of ASA on heat responses in primary nociceptive neurons by whole-cell patch-clamp and calcium microfluorimetry experiments. Heat-evoked inward currents in acutely dissociated rat dorsal root ganglion neurons were significantly reduced by ASA in a dose-dependent and reversible manner (IC(50) 375 nM, Hill slope -2.2, maximum effect 55%). Heat-evoked calcium transients (measured with FURA-2) were reversibly reduced by 53+/-14% (P0.05) by co-application of 1 microM ASA. The low IC(50) value, the rapid occurrence, and the reversibility of the observed effects make it unlikely that inhibition of prostaglandin synthesis is involved in the inhibition of nociceptive heat responses by ASA, and suggest a more direct effect on heat transduction mechanisms.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 2002-02-19 | Neuroscience Letters |