Is nitric oxide involved in 5-HT3 receptor-mediated neurogenic relaxation of guinea pig proximal colon?
Jazyk angličtina Země Japonsko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
9749926
DOI
10.1254/jjp.77.265
Knihovny.cz E-zdroje
- MeSH
- antagonisté serotoninu farmakologie MeSH
- hemoglobiny farmakologie MeSH
- hladké svalstvo účinky léků inervace MeSH
- indoly farmakologie MeSH
- inhibitory enzymů farmakologie MeSH
- kolon účinky léků inervace MeSH
- methylenová modř farmakologie MeSH
- morčata MeSH
- nitroarginin farmakologie MeSH
- ondansetron farmakologie MeSH
- oxid dusnatý antagonisté a inhibitory fyziologie MeSH
- receptory serotoninové 5-HT3 MeSH
- receptory serotoninové aplikace a dávkování účinky léků fyziologie MeSH
- relaxace svalu účinky léků MeSH
- synthasa oxidu dusnatého, typ I MeSH
- synthasa oxidu dusnatého antagonisté a inhibitory MeSH
- techniky in vitro MeSH
- tropisetron 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
- antagonisté serotoninu MeSH
- hemoglobiny MeSH
- indoly MeSH
- inhibitory enzymů MeSH
- methylenová modř MeSH
- nitroarginin MeSH
- ondansetron MeSH
- oxid dusnatý MeSH
- receptory serotoninové 5-HT3 MeSH
- receptory serotoninové MeSH
- synthasa oxidu dusnatého, typ I MeSH
- synthasa oxidu dusnatého 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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