Voluntary wheel running attenuates ethanol withdrawal-induced increases in seizure susceptibility in male and female rats

• Published in: Pharmacology, biochemistry and behavior Vol. 103; no. 1; pp. 18 - 25
• Main Authors: Devaud, Leslie L., Walls, Shawn A., McCulley, Walter D., Rosenwasser, Alan M.
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.11.2012
• Subjects: Alcohol Withdrawal Seizures - blood; Alcohol Withdrawal Seizures - etiology; Alcohol Withdrawal Seizures - prevention & control; Animals; Convulsants - toxicity; Ethanol - blood; Ethanol liquid diet; Ethanol withdrawal; Female; Male; Pentylenetetrazole - toxicity; Physical Exertion - physiology; Rats; Sex Characteristics; Sex differences; Substance Withdrawal Syndrome - blood; Substance Withdrawal Syndrome - prevention & control; Substance Withdrawal Syndrome - therapy; Wheel running; Ethanol withdrawal; Wheel running; Sex differences; Ethanol liquid diet
• ISSN: 0091-3057; 1873-5177
• DOI: 10.1016/j.pbb.2012.07.012

We recently found that voluntary wheel running attenuated ethanol withdrawal-induced increased susceptibility to chemoconvulsant-induced seizures in male rats. Since female rats recover from ethanol withdrawal (EW) more quickly than male rats across several behavioral measures, this study was designed to determine whether the effects of exercise on EW seizures also exhibited sex differences. Animals were maintained under no-wheel, locked-wheel or free-wheel conditions and ethanol was administered by liquid diet for 14days with control animals pair-fed an isocaloric diet, after which seizure thresholds were determined at 1day or 3days of EW. Consistent with previous reports, females ran significantly more than males, regardless of diet condition. Introduction of the ethanol-containing liquid diet dramatically increased running for females during the day (rest) phase, with little impact on night phase activity. Consistent with previous reports, EW increased seizure susceptibility at 1day in non-exercising males and females and at 3days in males. These effects were attenuated by access to running wheels in both sexes. We also assessed the effects of sex, ethanol diet and exercise on ethanol clearance following an acute ethanol administration at 1day EW in a separate set of animals. Blood ethanol concentrations at 30min post-injection were lower in males, ethanol-exposed animals, and runners, but no interactions among these factors were detected. Interestingly, females displayed more rapid ethanol clearance than males and there were no effects of either diet or wheel access on clearance rates. Taken together, these data suggest that voluntary wheel running during ethanol administration provides protective effects against EW seizures in both males and females. This effect may be mediated, in part, in male, but not in female rat, by effects of exercise on early pharmacokinetic contributions. This supports the idea that encouraging alcoholics to exercise may benefit their recovery. ► Wheel running protected against ethanol withdrawal seizure sensitivity in both male and female rats. ► The ethanol diet altered wheel-running activity during both active and rest phases. ► There were sex differences in wheel running and ethanol withdrawal responses.