PMID- 15582030 OWN - NLM STAT- MEDLINE DCOM- 20050512 LR - 20131121 IS - 0091-3057 (Print) IS - 0091-3057 (Linking) VI - 79 IP - 3 DP - 2004 Nov TI - Estrogen protects against brain lipid peroxidation in ethanol-withdrawn rats. PG - 573-86 AB - This study examined whether 17beta-estradiol (E2) administration protects against ethanol withdrawal (EW)-associated oxidative insults by assessing oxidative markers thiobarbituric-acid-reacting-substances (TBARS). Ovariectomized rats implanted with E2 (EW/E2) or oil pellets (EW/Oil) received chronic ethanol (7.5% wt./vol., 5 weeks) or control dextrin diet (Dextrin/Oil). At 24 or 48 h of EW, rats were tested for overt EW signs and the cerebellum, hippocampus, and cortex were prepared for TBARS assessment in the presence and absence of FeCl3. For control experiments, we assessed E2 effects on blood ethanol concentrations and TBARS levels during ethanol exposure prior to EW. The EW/Oil group showed enhanced endogenous- and FeCl3-stimulated membrane TBARS levels in the cerebellum and hippocampus in a manner inhibited by E2 treatment. There was a relationship between the severity of EW and elevation of TBARS levels, particularly in the cerebellum. The enhanced TBARS levels at 24 h of EW appeared to diminish at 48 h in the hippocampus, but persisted in the cerebellum. E2 treatment did not alter blood ethanol concentrations and ethanol exposure alone did not enhance TBARS levels. These data suggest that EW rather than ethanol enhances brain lipid peroxidation that is transient and brain-region specific. Estrogens protect against the brain lipid peroxidation in a manner independent of blood ethanol concentrations. FAU - Jung, Marianna E AU - Jung ME AD - Department of Pharmacology and Neuroscience, University of North Texas Health Science Center at Fort Worth, 3500 Camp Bowie Boulevard, Fort Worth, TX 76107-2699, USA. mjung@hsc.unt.edu FAU - Rewal, Mridula AU - Rewal M FAU - Perez, Evelyn AU - Perez E FAU - Wen, Yi AU - Wen Y FAU - Simpkins, James W AU - Simpkins JW LA - eng GR - AA013864/AA/NIAAA NIH HHS/United States PT - Comparative Study PT - Journal Article PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - Pharmacol Biochem Behav JT - Pharmacology, biochemistry, and behavior JID - 0367050 RN - 0 (Estrogens) RN - 3K9958V90M (Ethanol) SB - IM MH - Alcohol Drinking/drug therapy/metabolism MH - Animals MH - Brain/*drug effects/metabolism MH - Estrogens/*pharmacology/therapeutic use MH - Ethanol/*pharmacology MH - Female MH - Lipid Peroxidation/*drug effects/physiology MH - Ovariectomy MH - Rats MH - Substance Withdrawal Syndrome/*drug therapy/metabolism EDAT- 2004/12/08 09:00 MHDA- 2005/05/13 09:00 CRDT- 2004/12/08 09:00 PHST- 2004/06/07 00:00 [received] PHST- 2004/09/09 00:00 [revised] PHST- 2004/09/10 00:00 [accepted] PHST- 2004/12/08 09:00 [pubmed] PHST- 2005/05/13 09:00 [medline] PHST- 2004/12/08 09:00 [entrez] AID - S0091-3057(04)00297-7 [pii] AID - 10.1016/j.pbb.2004.09.007 [doi] PST - ppublish SO - Pharmacol Biochem Behav. 2004 Nov;79(3):573-86. doi: 10.1016/j.pbb.2004.09.007.