Partition of bispyridinium oximes (trimedoxime and K074) administered in therapeutic doses into different parts of the rat brain
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
PubMed
21146949
DOI
10.1016/j.jpba.2010.11.024
PII: S0731-7085(10)00667-9
Knihovny.cz E-zdroje
- MeSH
- butany aplikace a dávkování krev izolace a purifikace farmakokinetika farmakologie MeSH
- injekce intramuskulární MeSH
- kalibrace MeSH
- krysa rodu Rattus MeSH
- limita detekce MeSH
- molekulární struktura MeSH
- mozek metabolismus MeSH
- oximy aplikace a dávkování krev izolace a purifikace farmakokinetika farmakologie MeSH
- potkani Wistar MeSH
- pyridinové sloučeniny aplikace a dávkování krev izolace a purifikace farmakokinetika farmakologie MeSH
- reaktivátory cholinesterázy aplikace a dávkování krev izolace a purifikace farmakokinetika farmakologie MeSH
- referenční standardy MeSH
- regresní analýza MeSH
- reprodukovatelnost výsledků MeSH
- tkáňová distribuce MeSH
- trimedoxim aplikace a dávkování krev izolace a purifikace farmakokinetika farmakologie MeSH
- vysokoúčinná kapalinová chromatografie přístrojové vybavení 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
- 1,4-bis(4-hydroxyiminomethylpyridinium)butane dibromide MeSH Prohlížeč
- butany MeSH
- oximy MeSH
- pyridinové sloučeniny MeSH
- reaktivátory cholinesterázy MeSH
- trimedoxim MeSH
The penetration of acetylcholinesterase reactivators (oximes) into the central nervous system is typically restricted by the blood-brain barrier. Although oximes are highly hydrophilic compounds, some contradictory results confirming permeation into the brain exist. The aim of this study is to verify the penetration of oximes through the blood-brain barrier and to detect their levels achieved in different brain regions 60 min after the administration. It was confirmed that oximes are able to penetrate into the brain after injection of therapeutic doses corresponding with 5% of LD(50). The level in whole brain was 0.58% for trimedoxime and 0.85% for the experimental drug oxime K074 as the percentage of their plasma concentration. The highest concentration was found in frontal cortex (trimedoxime 2.27%; oxime K074 0.95%) and lowest in basal ganglia (trimedoxime 0.86%; oxime K074 0.42%). Entry of oximes into the brain is minimal, but some low reactivation effect should be expected. The reactivation potency of oximes might be higher or lower, depending on the real oxime concentration in a given area.
Citace poskytuje Crossref.org
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