Background: The method of continual determination of the rat blood cholinesterase activity was developed to study the changes of the blood cholinesterases following different intervetions. Aims: The aim of this study is registration of cholinesterase activity in the rat blood and its changes to demonstrate detoxification capacity of rats to inactivate sarin or VX in vivo. Methods: The groups of female rats were premedicated (ketamine and xylazine) and cannulated to a. femoralis. Continual blood sampling (0.02 ml/min) and monitoring of the circulating blood cholinesterase activity were performed. Normal activity was monitored 1–2 min and then the nerve agent was administered i.m. (2× LD50). Using different time intervals of the leg compressi...
Traditional multidrug therapy of organophosphorus nerve agent poisoning has several drawbacks such a...
We report the first toxicokinetic studies of (±)-sarin. The toxicokinetics of the stereoisomers of t...
The in vitro and in vivo reactivating power of 1,3-acetone- bis-(4-hydroxyiminoformyl pyridinium) di...
Determination of acetylcholinesterase activity in the rat brain after VX intoxication and following ...
Nerve agents belong to the most important group of highly toxic substances. The threat of their use ...
Organophosphorus esters (OPs) were originally developed as pesticides but were repurposed as easily ...
The aim of present work was a comparison of effectiveness of oximes chosen in the experimental thera...
Organophosphates (OPs) are used in agriculture via pesticides, and warfare and terrorism via nerve a...
Cholinesterase (ChE) is an enzyme which allows neurons to return to a resting state by hydrolyzing t...
Organophosphate compounds have been widely developed as pesticides (e.g. paraoxon) and also as chemi...
A computer simulation model of blood cholinesterase inhibition in rats resulting from a single oral ...
Protection experiments were conducted using different doses of equine serum butyrylcholinesterase (E...
International audienceOrganophosphorus nerve agents, like VX, are highly toxic due to their strong i...
Inhibition of acetylcholinesterase (AChE) is regarded as the primary toxic mechanism of organophosph...
Summary: In vivo effects of reversible inhibitors of cholinesterase activity were determined radiome...
Traditional multidrug therapy of organophosphorus nerve agent poisoning has several drawbacks such a...
We report the first toxicokinetic studies of (±)-sarin. The toxicokinetics of the stereoisomers of t...
The in vitro and in vivo reactivating power of 1,3-acetone- bis-(4-hydroxyiminoformyl pyridinium) di...
Determination of acetylcholinesterase activity in the rat brain after VX intoxication and following ...
Nerve agents belong to the most important group of highly toxic substances. The threat of their use ...
Organophosphorus esters (OPs) were originally developed as pesticides but were repurposed as easily ...
The aim of present work was a comparison of effectiveness of oximes chosen in the experimental thera...
Organophosphates (OPs) are used in agriculture via pesticides, and warfare and terrorism via nerve a...
Cholinesterase (ChE) is an enzyme which allows neurons to return to a resting state by hydrolyzing t...
Organophosphate compounds have been widely developed as pesticides (e.g. paraoxon) and also as chemi...
A computer simulation model of blood cholinesterase inhibition in rats resulting from a single oral ...
Protection experiments were conducted using different doses of equine serum butyrylcholinesterase (E...
International audienceOrganophosphorus nerve agents, like VX, are highly toxic due to their strong i...
Inhibition of acetylcholinesterase (AChE) is regarded as the primary toxic mechanism of organophosph...
Summary: In vivo effects of reversible inhibitors of cholinesterase activity were determined radiome...
Traditional multidrug therapy of organophosphorus nerve agent poisoning has several drawbacks such a...
We report the first toxicokinetic studies of (±)-sarin. The toxicokinetics of the stereoisomers of t...
The in vitro and in vivo reactivating power of 1,3-acetone- bis-(4-hydroxyiminoformyl pyridinium) di...