Is nitric oxide involved in 5-HT3 receptor-mediated neurogenic relaxation of guinea pig proximal colon?
Language English Country Japan Media print
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
9749926
DOI
10.1254/jjp.77.265
Knihovny.cz E-resources
- MeSH
- Serotonin Antagonists pharmacology MeSH
- Hemoglobins pharmacology MeSH
- Muscle, Smooth drug effects innervation MeSH
- Indoles pharmacology MeSH
- Enzyme Inhibitors pharmacology MeSH
- Colon drug effects innervation MeSH
- Methylene Blue pharmacology MeSH
- Guinea Pigs MeSH
- Nitroarginine pharmacology MeSH
- Ondansetron pharmacology MeSH
- Nitric Oxide antagonists & inhibitors physiology MeSH
- Receptors, Serotonin, 5-HT3 MeSH
- Receptors, Serotonin administration & dosage drug effects physiology MeSH
- Muscle Relaxation drug effects MeSH
- Nitric Oxide Synthase Type I MeSH
- Nitric Oxide Synthase antagonists & inhibitors MeSH
- In Vitro Techniques MeSH
- Tropisetron 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
- Serotonin Antagonists MeSH
- Hemoglobins MeSH
- Indoles MeSH
- Enzyme Inhibitors MeSH
- Methylene Blue MeSH
- Nitroarginine MeSH
- Ondansetron MeSH
- Nitric Oxide MeSH
- Receptors, Serotonin, 5-HT3 MeSH
- Receptors, Serotonin MeSH
- Nitric Oxide Synthase Type I MeSH
- Nitric Oxide Synthase MeSH
- Tropisetron MeSH
The relaxations mediated by the activation of 5-HT receptors in the guinea pig proximal colon were investigated. Longitudinal strips were cut from the colon segment and placed into the bath. In the presence of atropine (0.2 microM), the relaxations were evoked by adding increasing concentrations of 5-HT (1-100 microM). Noncumulative concentration-response curves were established in the absence and presence of either 5-HT or nitric oxide synthase (NOS) antagonists. Selective 5-HT3 antagonists tropisetron (10 and 100 nM) and ondansetron (1 microM) inhibited the relaxations and shifted the concentration-response curves to the right. Similar effects were observed in the presence of the NOS inhibitor N(G)-nitro-L-arginine (3.2, 10, 32 microM) and partly reversed with L-arginine (100, 320 microM). N(G)-nitro-D-arginine, serving as a negative control, was ineffective. The relaxations were further inhibited in the presence of the soluble guanylate cyclase blocker methylene blue (10 microM) or NO scavenger hemoglobin (32 microM). These results suggest that the 5-HT3 receptor plays a role in neurogenic relaxations of guinea pig proximal colon, which are at least partly mediated via release of NO from nerve endings.
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