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HLö - a review of acetylcholinesterase reactivator against organophosphorous intoxication
Miroslav Psotka, David Malinak, Lukas Gorecki, Thuy Duong Hguyen, Ondrej Soukup, Daniel Jun, Kamil Kuca, Kamil Musilek, Jan Korabecny
Jazyk angličtina Země Česko
Typ dokumentu práce podpořená grantem, přehledy
- Klíčová slova
- Hlo-t,
- MeSH
- acetylcholinesterasa fyziologie chemie MeSH
- chemické bojové látky otrava MeSH
- cholinesterasové inhibitory farmakologie terapeutické užití MeSH
- LD50 MeSH
- lidé MeSH
- nervová bojová látka otrava MeSH
- organofosforové sloučeniny MeSH
- otrava organofosfáty * farmakoterapie MeSH
- oximy MeSH
- pesticidy otrava MeSH
- pyridinové sloučeniny * farmakokinetika farmakologie chemická syntéza chemie terapeutické užití MeSH
- reaktivátory cholinesterázy * farmakokinetika farmakologie chemická syntéza chemie terapeutické užití MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- práce podpořená grantem MeSH
- přehledy MeSH
The treatment of organophosphate (OP) poisoning consists of the administration of a parasympatholytic agent, an anticonvulsant and an acetylcholinesterase (AChE) reactivator. Since there is no broad AChE reactivator available, a post-treatment strategy currently exploits administration of different types of oximes depending on the exposure of OP. In this contribution, we summarize all the available data about AChE reactivator HLö-7 including its synthesis, physico-chemical properties, pharmacokinetic and pharmacodynamics profile, and its efficacy in vitro and in vitro.
Literatura
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- $a The treatment of organophosphate (OP) poisoning consists of the administration of a parasympatholytic agent, an anticonvulsant and an acetylcholinesterase (AChE) reactivator. Since there is no broad AChE reactivator available, a post-treatment strategy currently exploits administration of different types of oximes depending on the exposure of OP. In this contribution, we summarize all the available data about AChE reactivator HLö-7 including its synthesis, physico-chemical properties, pharmacokinetic and pharmacodynamics profile, and its efficacy in vitro and in vitro.
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