Literature DB >> 9113264

Free radical production during ethanol intoxication, dependence, and withdrawal.

M Vallett1, T Tabatabaie, R J Briscoe, T J Baird, W W Beatty, R A Floyd, D V Gauvin.   

Abstract

Indices of free radical production and cell damage were examined in male Sprague-Dawley rats chronically exposed to either ethanol (ETOH) or water vapor. In experiment 1, rats experienced either 1 or 11 cycles of ETOH exposure and withdrawal. Brain tissue was harvested 12 hr after ETOH exposure, and 1 hr after being injected with sodium salicylate as a scavenger. Brain tissue was analyzed for the formation of salicylate hydroxylation products as a measure of .OH production during withdrawal. Significant group differences for .OH production were demonstrated for 2,3- and 2,5-dihydroxybenzoic acid in the single cycle ETOH exposed rats compared with their water cohorts. A significant between group difference for 2,5-dihydroxybenzoic acid, only, was demonstrated for the multiple cycles of ETOH exposure. Spontaneous seizures were shown to correlate with increased production of .OH in ETOH exposed rats. In experiment 2, brain tissue was harvested from different groups of rats after removal from the chambers, at 0, 2, 12, 24, 36, and 48 hr after a single exposure cycle. Tissue was analyzed for (1) salicylate hydroxylation (as above), (2) glutamine synthetase activity, (3) whole brain glutamate concentration, and (4) oxidized protein. A multiple regression analysis was conducted on the five dependent variables and found they could be predicted by specific behavioral and neurological ratings. These data suggest that cell damage during withdrawal may have multiple time-dependent components.

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Year:  1997        PMID: 9113264

Source DB:  PubMed          Journal:  Alcohol Clin Exp Res        ISSN: 0145-6008            Impact factor:   3.455


  11 in total

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Review 4.  Smoking and increased Alzheimer's disease risk: a review of potential mechanisms.

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5.  Protective effect of blackcurrant on liver cell membrane of rats intoxicated with ethanol.

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6.  Intermittent hypoxia conditioning prevents behavioral deficit and brain oxidative stress in ethanol-withdrawn rats.

Authors:  Marianna E Jung; James W Simpkins; Andrew M Wilson; H Fred Downey; Robert T Mallet
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7.  A Systems Approach Implicates a Brain Mitochondrial Oxidative Homeostasis Co-expression Network in Genetic Vulnerability to Alcohol Withdrawal.

Authors:  Nicole A R Walter; DeAunne L Denmark; Laura B Kozell; Kari J Buck
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Review 8.  Alcohol withdrawal and brain injuries: beyond classical mechanisms.

Authors:  Marianna E Jung; Daniel B Metzger
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9.  Phenolic compounds protect cultured hippocampal neurons against ethanol-withdrawal induced oxidative stress.

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