International Journal of Molecular Sciences · 2007 · 20 citations · 21 references
MedicinePharmacologyToxicologyNeurochemistryNeuropharmacologyPharmaceutical ToxicologyCentral Nervous System Drug ActionsCentral Nervous System ToxicityCholinergic NeurochemistryCholinergic PharmacologyNeurochemical PharmacologyNeuroprotectionAcetylcholine PharmacologyAcetylcholinesterase FunctionAcetylcholinesterase InhibitorsAche InhibitionBiochemical CharacterizationCentral Cholinergic PharmacologyNeurotoxicity Of DrugsRodent Neuropharmacology
Acetylcholinesterase (AChE) activities in different brain parts were determinedquantitatively in rats treated with huperzine A, soman, and huperzine A followed bysoman, using histochemical and biochemical methods. Following soman intoxication (1.2x LD50, i.m.), AChE activity was decreased to 30-80% of control values depending on thebrain structure. The most sensitive area was the frontal cortex and the most relativelyresistant was ncl. ruber. Huperzine A treatment only caused a change in AChE activityvarying from 70 to 100 % of control values. In rats pretreated with huperzine A andintoxicated with soman, AChE activity was significantly higher than that observed aftersoman. In these animals, survival of rats pretreated with huperzine was observed whilethe mortality of unpretreated animals was near to 80 %. The results suggest that huperzineA is good candidate for further study for clinical use as a prophylactic drug against nerveagent poisoning.
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A new and rapid colorimetric determination of acetylcholinesterase activity
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