MDP and 5-HT receptors. Does MDP interact with 5-HT(7) receptors?
Jazyk angličtina Země Velká Británie, Anglie Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
10988353
DOI
10.1016/s0192-0561(00)00021-7
PII: S0192056100000217
Knihovny.cz E-zdroje
- MeSH
- acetylmuramyl-alanyl-isoglutamin farmakologie MeSH
- adjuvancia imunologická farmakologie MeSH
- ileum účinky léků fyziologie MeSH
- metergolin farmakologie MeSH
- morčata MeSH
- receptory serotoninové účinky léků MeSH
- serotonin analogy a deriváty farmakologie MeSH
- vztah mezi dávkou a účinkem léčiva MeSH
- zvířata MeSH
- Check Tag
- morčata MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 5-carboxamidotryptamine MeSH Prohlížeč
- acetylmuramyl-alanyl-isoglutamin MeSH
- adjuvancia imunologická MeSH
- metergolin MeSH
- receptory serotoninové MeSH
- serotonin 7 receptor MeSH Prohlížeč
- serotonin MeSH
A possible interaction of immunomodulator muramyl dipeptide (MDP) with 5-HT(7) (5-hydroxytryptamine) receptors was investigated. The activation of 5-HT(7) receptors relaxes the guinea-pig distal ileum. The whole ileum segments were, therefore, cut and placed into the bath. The preparations were precontracted by substance P and potently relaxed by adding incremental concentrations of 5-carboxamidotryptamine (5-CT) (0.01-3.2 microM), less potently by 5-hydroxytryptamine (5-HT) (1-100 microM). The preparations most sensitive to 5-CT were also relaxed by MDP (1-100 microM). Noncumulative concentration-response curves (CRCs) for 5-HT or 5-CT were established in the absence or presence of 5-HT antagonist metergoline (320 nM). Metergoline inhibited the relaxations and shifted the CRCs to the right. In the preparations most sensitive to the effects of both 5-CT and metergoline, the latter substance also inhibited the effect of the highest concentration (100 microM) in CRCs for MDP. In another type of experiments, CRCs for 5-HT or 5-CT were constructed in the presence of low concentrations of MDP (5-500 nM). The relaxations evoked by either drug remained unchanged. These results suggest that low concentrations of MDP do not interact with activation of 5-HT(7) receptors. In higher concentrations MDP acts on this receptor type as a very weak partial agonist.
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