MDP and 5-HT receptors. Does MDP interact with 5-HT(7) receptors?
Language English Country Great Britain, England Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
10988353
DOI
10.1016/s0192-0561(00)00021-7
PII: S0192056100000217
Knihovny.cz E-resources
- MeSH
- Acetylmuramyl-Alanyl-Isoglutamine pharmacology MeSH
- Adjuvants, Immunologic pharmacology MeSH
- Ileum drug effects physiology MeSH
- Metergoline pharmacology MeSH
- Guinea Pigs MeSH
- Receptors, Serotonin drug effects MeSH
- Serotonin analogs & derivatives pharmacology MeSH
- Dose-Response Relationship, Drug MeSH
- Animals MeSH
- Check Tag
- Guinea Pigs MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- 5-carboxamidotryptamine MeSH Browser
- Acetylmuramyl-Alanyl-Isoglutamine MeSH
- Adjuvants, Immunologic MeSH
- Metergoline MeSH
- Receptors, Serotonin MeSH
- serotonin 7 receptor MeSH Browser
- 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.
References provided by Crossref.org