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Gewählte Publikation:

Lembeck, F; Popper, H; Juan, H.
Release of prostaglandins by bradykinin as an intrinsic mechanism of its algesic effect.
Naunyn Schmiedebergs Arch Pharmacol. 1976; 294(1):69-73 Doi: 10.1007/BF00692786
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Co-Autor*innen der Med Uni Graz
Popper Helmuth
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Abstract:
1. The release of PGs from the isolated perfused rabbit ear was measured by means of a radioimmunoassay. 2. Bradykinin in dose dependent amounts released mainly PGE (presumably PGE1) and in much smaller amounts also PGF. 3. Bradykinin released similar amounts of PGE in innervated and chronically denervated ears. 4. Indomethacin completely prevented the PGE release by bradykinin. 5. ACh showed a much lower efficacy than bradykinin in releasing PGE and PGF. Synthetic substance P was devoid of any PGE releasing action. 6. It is concluded that bradykinin increases its own algesic action by a concomitant rapid stimulation of the PGE synthesis, thus providing a mechanism for the facilitation of its own algesic action.
Find related publications in this database (using NLM MeSH Indexing)
Acetylcholine - pharmacology
Animals - pharmacology
Bradykinin - antagonists and inhibitors
Denervation - antagonists and inhibitors
Ear - antagonists and inhibitors
Indomethacin - pharmacology
Pain - chemically induced
Prostaglandins - metabolism
Prostaglandins E - biosynthesis
Rabbits - biosynthesis
Substance P - pharmacology

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