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]
Web of Science
PubMed
FullText
FullText_MUG
Google Scholar
- Co-Autor*innen der Med Uni Graz
-
Holzer Peter
-
Lembeck Fred
- Altmetrics:
- Dimensions Citations:
- Plum Analytics:
- Scite (citation analytics):
- 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