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Gewählte Publikation:

Barthó, L; Holzer, P; Lembeck, F; Szolcsányi, J.
Evidence that the contractile response of the guinea-pig ileum to capsaicin is due to release of substance P.
J PHYSIOL-LONDON 1982 332: 157-167. Doi: 10.1113/jphysiol.1982.sp014407 [OPEN ACCESS]
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Co-Autor*innen der Med Uni Graz
Holzer Peter
Lembeck Fred
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Abstract:
1. The possible roles of substance P and opioids in the contractile response of the isolated guinea-pig ileum to the sensory stimulant drug capsaicin were investigated, and the contractions were found to be inhibited by about 60% in preparations desensitized to substance P. 2. Contractions evoked by stimulation of the mesenteric nerves in the presence of the adrenergic blocking drug guanethidine were inhibited by about 75% after the ileum had been rendered insensitive to substance P. 3. Atropine partially inhibited the effect of capsaicin. The atropine-resistant component of the contractile response to capsaicin was inhibited by more than 85% in preparations desensitized to substance P and almost abolished by the substance P antagonist, (D-Pro2,D-Trp7,9)-substance P. 4. The opioid peptide (D-Met2, Pro5)-enkephalinamide inhibited, whereas the opiate antagonist naloxone enhanced the atropine-resistant contractions in response to capsaicin. 5. The results indicate that the contractile response of the guinea-pig ileum to capsaicin and mesenteric nerve stimulation is mediated by release of substance P, presumably from sensory nerve endings in the gut. Substance P appears to act on the smooth muscle both directly and indirectly via cholinergic neurones. It is proposed that opioids modulate the non-cholinergic response to capsaicin by inhibiting the release of substance P.
Find related publications in this database (using NLM MeSH Indexing)
Animals -
Atropine - pharmacology
Capsaicin - pharmacology
Endorphins - pharmacology
Fatty Acids, Unsaturated - pharmacology
Guanethidine - pharmacology
Guinea Pigs - pharmacology
Ileum - physiology
In Vitro - physiology
Muscle Contraction - drug effects
Muscle, Smooth - physiology
Naloxone - pharmacology
Research Support, Non-U.S. Gov't - pharmacology
Substance P - antagonists and inhibitors

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