Carnosine and other imidazole-containing compounds enhance the postdenervation depolarization of the rat diaphragm fibres
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
9803477
Knihovny.cz E-zdroje
- MeSH
- anserin farmakologie MeSH
- bránice inervace MeSH
- denervace svalu * MeSH
- donory oxidu dusnatého farmakologie MeSH
- imidazoly farmakologie MeSH
- indazoly farmakologie MeSH
- inhibitory enzymů farmakologie MeSH
- karnosin farmakologie MeSH
- krysa rodu Rattus MeSH
- kyselina glutamová farmakologie MeSH
- membránové potenciály účinky léků MeSH
- nitroprusid farmakologie MeSH
- oxid dusnatý metabolismus MeSH
- potkani Wistar MeSH
- synthasa oxidu dusnatého antagonisté a inhibitory MeSH
- zvířata MeSH
- Check Tag
- krysa rodu Rattus MeSH
- mužské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Názvy látek
- 7-nitroindazole MeSH Prohlížeč
- anserin MeSH
- donory oxidu dusnatého MeSH
- imidazoly MeSH
- indazoly MeSH
- inhibitory enzymů MeSH
- karnosin MeSH
- kyselina glutamová MeSH
- nitroprusid MeSH
- oxid dusnatý MeSH
- synthasa oxidu dusnatého MeSH
In the presence of carnosine, anserine, histidine, imidazole and 7-nitro indazole, the early postdenervation depolarization of muscle of about 8 mV was significantly increased by 2.15-4.8 mV. The presence of the imidazole ring in the molecule is apparently necessary for this effect. These compounds also eliminated an NO-mediated protective effect of L-glutamate and carbachol on the depolarization of membrane potential. The presence of imidazole, 7-nitro indazole, carnosine and anserine did not significantly change the effect of an external NO donor, sodium nitroprusside. The structural and functional similarity between imidazole derivatives and the known NO synthase inhibitor, 7-nitro indazole suggests that imidazole, carnosine and anserine might act by inhibiting NO production which is stimulated by glutamate and carbachol.
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