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      Peripheral analgesia: mechanism of the analgesic action of aspirin-like drugs and opiate-antagonists.

      British Journal of Clinical Pharmacology
      Analgesics, Animals, Aspirin, pharmacology, Calcium, metabolism, Cyclic AMP, Epoprostenol, Hyperalgesia, Morphine, Narcotic Antagonists, Pain, chemically induced, Prostaglandins

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          Abstract

          1 Prostaglandins released by tissue injury sensitize nociceptors and produce hyperalgesia. 2 Aspirin-like drugs inhibit prostaglandins I2 and E2, synthesis, which explains their anti-algic effect. 3 The anti-algic effect of aspirin-like drugs in carrageenin-induced rat paw inflammation may involve a central component. 4 Prostaglandin E2-induced hyperalgesia, once established, is not relieved by systemically administered drugs. 5 Prostaglandin-induced hyperalgesia is possibly a cyclic adenosine, 3',5'-monophosphate C2+ dependent process. 6 Morphine, enkephalins, opiate antagonists and cyclic guanosine 3',5'-monophosphate have a peripheral analgesic effect in the prostaglandin hyperalgesia test. 7 Morphine may produce peripheral analgesia by inhibiting adenylatecyclase activity at the nociceptors.

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          Author and article information

          Journal
          6254551
          1430169
          10.1111/j.1365-2125.1980.tb01806.x

          Chemistry
          Analgesics,Animals,Aspirin,pharmacology,Calcium,metabolism,Cyclic AMP,Epoprostenol,Hyperalgesia,Morphine,Narcotic Antagonists,Pain,chemically induced,Prostaglandins

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