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I - Prostaglandin hyperalgesia, a cAMP/Ca2+ dependent process.

S H Ferreira·M Nakamura
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Abstract

Prostaglandins stimulate cAMP increase in several biological systems including CNS. The possible participation of a cAMP/Ca2+ related mechanism in prostaglandin induced hyperalgesia in the rat paw, as measured by a modification of the Randall-Selitto method was investigated. A serie of agents was administered in the paw in an attempt to change either Ca2+ or cyclic AMP concentration at the nociceptive terminations. PGE2, dibutyryl cyclic AMP, isoprenaline, noradrenaline, adrenaline, Ca2+ionophore (A23187), BaCl2 caused a dose dependent hyperalgesia. The hyperalgesic effect of these substances was enhanced by methyl-xanthines. Cyclic GMP as well as agents which interfere with Ca2+ influx (verapamil and lanthanum) were local analgesics in normal and hyperalgesic paws.

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AnalgesicsAnimalsBariumBucladesineCalcimycinCalciumCatecholaminesCyclic AMPDrug SynergismHyperalgesiaHyperesthesiaNociceptorsProstaglandins ERatsXanthinesJournal Article

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S H Ferreira, M Nakamura. 1979. I - Prostaglandin hyperalgesia, a cAMP/Ca2+ dependent process.. https://doi.org/10.1016/0090-6980(79)90103-5

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