The effect of alpha-phenyl-N-tert-butyl nitrone on bioenergetic state in substantia nigra following flurothyl-induced status epilepticus in rats
Language English Country Ireland Media print
Document type Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.
PubMed
10353342
DOI
10.1016/s0304-3940(99)00279-7
PII: S0304-3940(99)00279-7
Knihovny.cz E-resources
- MeSH
- Cyclic N-Oxides MeSH
- Energy Metabolism drug effects MeSH
- Flurothyl toxicity MeSH
- Convulsants toxicity MeSH
- Rats MeSH
- Nitrogen Oxides pharmacology MeSH
- Rats, Wistar MeSH
- Free Radical Scavengers pharmacology MeSH
- Spin Labels MeSH
- Status Epilepticus chemically induced drug therapy metabolism MeSH
- Substantia Nigra drug effects metabolism MeSH
- Animals MeSH
- Check Tag
- Rats MeSH
- Male MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Research Support, U.S. Gov't, P.H.S. MeSH
- Names of Substances
- Cyclic N-Oxides MeSH
- Flurothyl MeSH
- Convulsants MeSH
- Nitrogen Oxides MeSH
- phenyl-N-tert-butylnitrone MeSH Browser
- Free Radical Scavengers MeSH
- Spin Labels MeSH
Status epilepticus (SE), i.e. ongoing seizures of more than 30 min duration, gives rise to bilateral pan-necrotic lesions of the substantia nigra, pars reticulata (SNPR). These are known to be preceded by an initial increase, followed by a depression of metabolic rate, and by failure of the bioenergetic state, suggesting mitochondrial dysfunction. We have previously shown that the spin trap alpha-phenyl-N-tert-butyl nitrone (PBN) prevents the lesions caused by 45 min of SE from occurring, in spite of ongoing seizure activity. In this article, we demonstrate that PBN, given 30 min before seizure induction, reduces or prevents the decrease in ATP concentration and adenylate energy charge, without significantly reducing the amount of lactate accumulated, or the decrease in intracellular pH (pHi). The results suggest that the spin trap nitrone preserves the structural and functional integrity of SNPR neurons by protecting the mitochondria against oxidative damage.
References provided by Crossref.org
Epilepsy Research in the Institute of Physiology of the Czech Academy of Sciences in Prague