Transport of an antihypoxic drug stobadine across the blood-brain barrier in rat striatum and its influence on catecholamine-oxidative current: a voltammetric study under normal and anoxic/ischaemic conditions
Jazyk angličtina Země Česko Médium print
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
9200210
Knihovny.cz E-zdroje
- MeSH
- biologický transport MeSH
- corpus striatum metabolismus MeSH
- dopamin metabolismus farmakologie MeSH
- elektrofyziologie MeSH
- hematoencefalická bariéra fyziologie MeSH
- ischemie mozku metabolismus MeSH
- karboliny krev farmakokinetika farmakologie MeSH
- katecholaminy analýza metabolismus MeSH
- krysa rodu Rattus MeSH
- mikroelektrody MeSH
- mozková hypoxie metabolismus MeSH
- oxidace-redukce MeSH
- potkani Wistar 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
- dicarbine MeSH Prohlížeč
- dopamin MeSH
- karboliny MeSH
- katecholaminy MeSH
Differential pulse voltammetry with a carbon fibre microelectrode (ME) was used in pentobarbital-anaesthetized rats for monitoring the stobadine current (STB.C) on both sides of the blood-brain barrier (BBB) in the arterial bloodstream (BS) and in the corpus striatum (CS). The STB.C exhibited a distinct peak at a polarization voltage 540 +/- 30 mV (n = 4). The maximum of STB.C in BS attained 2-3 min after the STB administration (2.8 mg/100 g in 1.0 ml saline solution i.a.) was followed by a rapid decrease to about 20% within next 3 min. The STB readily passed across the BBB: the STB.C peak appeared in the CS in the 3rd minute and continued to rise up to the 30th min. The administration of STB did not prevent a large increase (1347 +/- 326%, n = 3) of the catechol-oxidative current (CA.OC) occurring in the CS between the 4th and 5th minute after cardiac arrest. However, a decrease of ME sensitivity to CA.OC in the presence of STB was observed. This fact leads to the speculation whether a similar "quenching" of dopamine by STB could not participate in the protective effects of STB observed in the brain exposed to hypoxia-reoxygenation.