PubMed · 2010 · 16 citations · 19 references
PharmacyNeurosciencePharmacologyNeurochemistryNeuropharmacologyNeurotoxicologyCentral Nervous System ToxicityCyanide ToxicologyNeuroprotectionNeuroprotective PharmacologyNeurotoxic MechanismsNeurotoxicity MechanismsAcute Cyanide PoisoningBrain RegionsCyanide MetabolismCytochrome Oxidase InhibitionHypoxiaMechanisms Of Cyanide ToxicityNeuroprotective MechanismsRespiratory Enzyme Inhibition
Cyanide is a potential suicidal, homicidal and chemical warfare agent. It produces histotoxic hypoxia following inhibition of cytochrome c oxidase, a terminal respiratory chain enzyme. The profound metabolic changes lead to neurotoxicity including alterations in the levels of neurotransmitters. The present study addressed the effect of acute exposure of lethal and sub-lethal doses of potassium cyanide (KCN; 0.75 or 2.0 LD50; po) on the levels of neurotransmitters in discrete brain regions of rats and its response to treatment with alpha-ketoglutarate (alpha-KG; 0.5 g/kg; po; -10 min) alone or with sodium thiosulphate (STS; 1.0 g/kg; ip; -15 min). KCN significantly decreased norepinephrine, dopamine and 5-hydroxytryptamine levels in different brain regions which were resolved by alpha-KG and/or STS. Corpus striatum and hippocampus were more sensitive as compared to cerebral cortex and hypothalamus. alpha-KG, a potential cyanide antidote alone or with STS showed neuroprotective effects against cyanide.
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A re-examination of the reactions of cyanide with cytochrome <i>c</i> oxidase
M G Jones, David Bickar, Michael T. Wilson et al. · Biochemical Journal · 1984 · 151 citations · Full text