Effects of soman poisoning on mitochondrial respiratory enzyme activity in the mouse hippocampus and cerebral cortex

References

• Acharya MM, Katyare SS. (2005). Structural and functional alterations in mitochondrial membrane in picrotoxin-induced epileptic rat brain. Exp Neurol 192:79–88.
   PubMed Web of Science ®Google Scholar
• Cáceda R, Gamboa JL, Boero JA, Monge C, Arregui A. (2001). Energetic metabolism in mouse cerebral cortex during chronic hypoxia. Neurosci Lett 301:171–174.
   PubMed Web of Science ®Google Scholar
• Carpentier P, Foquin A, Kamenka JM, Rondouin G, Lerner-Natoli M, De Groot DMG, et al. (2001). Effects of thienylphencyclidine (TPC) on seizure activity and brain damage produced by soman in guinea pigs: EcoG correlates of neurotoxicity. NeuroToxicology 22:13–28.
   PubMed Web of Science ®Google Scholar
• Chuang YC, Chang AYW, Lin JW, Hsu SP, Chan SHH. (2004). Mitochondrial dysfunction and ultrastructural damage in the hippocampus during kainic acid-induced status epilepticus in the rat. Epilepsia 45:1202–1209.
   PubMed Web of Science ®Google Scholar
• Clarkson AN, Liu H, Pearson L, Kapoor M, Harrison JC, Sammut IA, et al. (2004). Neuroprotective effects of spermine following hypoxia-ischemia-induced brain damage: a mechanistic study. FASEB J 18:1114–1126.
   PubMed Web of Science ®Google Scholar
• Cock HR, Tong X, Hargreaves IP, Heales SJR, Clark JB, Patsalos PN, et al. (2002). Mitochondrial dysfunction associated with neuronal death following status epilepticus in rat. Epilepsy Res 48:157–168.
   PubMed Web of Science ®Google Scholar
• Collombet JM, Four E, Bernabé D, Masqueliez C, Burckhart MF, Baille V, et al. (2005). Soman poisoning increases neural progenitor proliferation and induces long-term glial activation in mouse. Toxicology 208:319–334.
   PubMed Web of Science ®Google Scholar
• Collombet JM, Carpentier P, Baille V, Four E, Bernabé D, Burckhart MF, et al. (2006). Neuronal regeneration partially compensates the delayed neuronal cell death observed in the hippocampal CA1 field of soman-poisoned mice. NeuroToxicology 27:201–209.
   PubMed Web of Science ®Google Scholar
• Collombet JM, Piérard C, Béracochéa D, Coubard S, Burckhart MF, Four E, et al. (2008). Long-term consequences of soman poisoning in mice—Part 1. Neuropathology and neuronal regeneration in the amygdala. Behav Brain Res 191:88–94.
   PubMed Web of Science ®Google Scholar
• Gao J, Chi ZF, Liu XW, Shan PY, Wang R. (2007). Mitochondrial dysfunction and ultrastructural damage in the hippocampus of pilocarpine-induced rat. Neurosci Lett 411:152–157.
   PubMed Web of Science ®Google Scholar
• Gupta RC, Dettbarn WD. (1987). Alterations of high-energy phosphate compounds in the skeletal muscles of rats intoxicated with diisopropylphosphorofluoridate (DFP) and soman. Fund Appl Toxicol 8:400–407.
   PubMedGoogle Scholar
• Jin Z, El-Deiry WS. (2005). Overview of cell death signaling pathways. Cancer Biol Ther 4:139–163.
   PubMed Web of Science ®Google Scholar
• Kann O, Kovács R. (2007). Mitochondria and neuronal activity. Am J Physiol Cell Physiol 292:C641–C657.
   PubMed Web of Science ®Google Scholar
• Kudin AP, Kudina TA, Seyfried J, Vielhaber S, Beck H, Elger CE, et al. (2002). Seizure-dependent modulation of mitochondrial oxidative phosphorylation in rat hippocampus. Eur J Neurosci 15:1105–1114.
   PubMed Web of Science ®Google Scholar
• Lallement G, Delamanche IS, Pernot-Marino I, Baubichon D, Denoyer M, Carpentier P, et al. (1993). Neuroprotective activity of glutamate antagonists against soman-induced hippocampal damage: quantification with an ω3 site ligand. Brain Res 618:227–237.
   PubMed Web of Science ®Google Scholar
• Lallement G, Dorandeu F, Filliat P, Carpentier P, Baille V, Blanchet G. (1998). Medical management of organophosphate-induced seizures. J Physiol (Paris) 92:369–373.
   Web of Science ®Google Scholar
• Lebeda FJ, Wierwille RC, VanMeter WG, Sikora-VanMeter KC. (1988). Acute ultrastructural alterations induced by soman and hypoxia in rat hippocampal CA3 pyramidal neurons. NeuroToxicology 9:9–22.
   PubMed Web of Science ®Google Scholar
• Lowry OH, Rosebrough NJ, Farr AL, Randall RJ. (1951). Protein measurement with the folin phenol reagent. J Biol Chem 193:265–275.
   PubMed Web of Science ®Google Scholar
• McDonough JH, Shih TM. (1997). Neuropharmacological mechanisms of nerve agent–induced seizure and neuropathology. Neurosci Biobehav Rev 21:559–579.
   PubMed Web of Science ®Google Scholar
• Milatovic D, Zivin M, Gupta RC, Dettbarn WD. (2001). Alterations in cytochrome c oxidase activity and energy metabolites in response to kainic acid-induced status epilepticus. Brain Res 912:67–78.
   PubMed Web of Science ®Google Scholar
• Miller AL, Medina MA. (1986). Cerebral metabolic effects of organophosphorus anticholinesterase compounds. Metab Brain Dis 1:147–156.
   PubMed Web of Science ®Google Scholar
• Mousson B, Collombet JM, Dumoulin R, Carrier H, Flocard F, Bouzidi M, et al. (1995). An abnormal exercise test response revealing a respiratory chain complex III deficiency. Acta Neurol Scand 91:488–493.
   PubMed Web of Science ®Google Scholar
• Sikora-VanMeter KC, Wierwille RC, Willetts EJ, VanMeter WG. (1987). Morphological evidence for increased protein synthesis in CNS neurons after soman exposure. Fund Appl Toxicol 8:23–38.
   PubMedGoogle Scholar
• Soane L, Kahraman S, Kristian T, Fiskum G. (2007). Mechanisms of impaired mitochondrial energy metabolism in acute and chronic neurodegenerative disorders. J Neurosci Res 85:3407–3415.
   PubMed Web of Science ®Google Scholar
• Srere PA. (1969). Citrate synthase. In: Lowenstein JM (Ed.), Methods in Enzymology, Vol. 13 ( pp 3–11). New-York: Academic Press.
   Google Scholar
• Tryphonas L, Veinot JP, Clement JG. (1996). Early histopathologic and ultrastructural changes in the heart of Sprague-Dawley rats following administration of soman. Toxicol Pathol 24:190–198.
   PubMed Web of Science ®Google Scholar