Sex differences in steroid modulation of ethanol withdrawal in male and female rats

被引:32
作者
Alele, P. E. [1 ]
Devaud, L. L. [1 ]
机构
[1] Idaho State Univ, Dept Pharmaceut Sci, Pocatello, ID 83209 USA
关键词
D O I
10.1124/jpet.106.107896
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We investigated the actions of the neuroactive steroid, pregnenolone, and the ovarian steroid, 17 beta- estradiol, on seizure expression during two time points of ethanol withdrawal ( EW). Both steroids can exert rapid, nongenomic actions on the brain that include modulation of seizure activity. Because their basal levels differ in adult males and females and a major symptom of EW is increased seizure risk, we wanted to determine whether these steroids were anticonvulsant during EW. Rats were made ethanol-dependent by administration of 6% ethanol in a nutritionally complete liquid diet for 14 days. After removal of the ethanol- containing diet, EW and paired control rats were tested at 1 or 3 days for seizure responses to pentylenetetrazol. Consistent with previous reports, females seemed to have recovered from EW more quickly than males. We observed significant sex differences in responses to the steroids, primarily at 3 days EW. Pregnanolone afforded protection against seizures with larger effects during EW than in control conditions and greater effects in female than male rats. In contrast, effects of estradiol were mixed. Some responses of ovariectomized female rats were similar to intact females, whereas other responses were more similar to males. Our behavioral findings are consistent with observed EW- induced changes in plasma corticosterone levels, showing persistent elevations in male but not female rats. These results support and extend earlier findings suggesting that although the hormonal milieu influences EW, innate differences in brain structure between the sexes also contribute to sex differences in EW.
引用
收藏
页码:427 / 436
页数:10
相关论文
共 37 条
[1]   Differential adaptations in GABAergic and glutamatergic systems during ethanol withdrawal in male and female rats [J].
Alele, PE ;
Devaud, LL .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2005, 29 (06) :1027-1034
[2]   MORBIDITY IN ALCOHOLICS - EVIDENCE FOR ACCELERATED DEVELOPMENT OF PHYSICAL DISEASE IN WOMEN [J].
ASHLEY, MJ ;
OLIN, JS ;
RICHE, WHL ;
KORNACZEWSKI, A ;
SCHMIDT, W ;
RANKIN, JG .
ARCHIVES OF INTERNAL MEDICINE, 1977, 137 (07) :883-887
[3]  
Baulieu EE, 1997, RECENT PROG HORM RES, V52, P1
[4]   Animal models of social stress: Effects on behavior and brain neurochemical systems [J].
Blanchard, RJ ;
McKittrick, CR ;
Blanchard, DC .
PHYSIOLOGY & BEHAVIOR, 2001, 73 (03) :261-271
[5]   The diversity of seizures related to alcohol use.: A study of consecutive patients [J].
Bråthen, G ;
Brodtkorb, E ;
Helde, G ;
Sand, T ;
Bovim, G .
EUROPEAN JOURNAL OF NEUROLOGY, 1999, 6 (06) :697-703
[6]   Stress enhancement of craving during sobriety:: A risk for relapse [J].
Breese, GR ;
Chu, K ;
Dayas, CV ;
Funk, D ;
Knapp, DJ ;
Koob, GF ;
Lê, DA ;
O'Dell, LE ;
Overstreet, DH ;
Roberts, AJ ;
Sinha, R ;
Valdez, GR ;
Weiss, F .
ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2005, 29 (02) :185-195
[7]   ALCOHOL DETOXIFICATION AND WITHDRAWAL SEIZURES - CLINICAL SUPPORT FOR A KINDLING HYPOTHESIS [J].
BROWN, ME ;
ANTON, RF ;
MALCOLM, R ;
BALLENGER, JC .
BIOLOGICAL PSYCHIATRY, 1988, 23 (05) :507-514
[8]   Chronic intermittent ethanol (CIE) administration in rats decreases levels of neurosteroids in hippocampus, accompanied by altered behavioral responses to neurosteroids and memory function [J].
Cagetti, E ;
Pinna, G ;
Guidotti, A ;
Baicy, K ;
Olsen, RW .
NEUROPHARMACOLOGY, 2004, 46 (04) :570-579
[9]   Alcoholic men endorse more DSM-IV withdrawal symptoms than alcoholic women matched in drinking history [J].
Deshmukh, A ;
Rosenbloom, MJ ;
Sassoon, S ;
O'Reilly, A ;
Pfefferbaum, A ;
Sullivan, EV .
JOURNAL OF STUDIES ON ALCOHOL, 2003, 64 (03) :375-379
[10]  
Devaud Leslie L., 2003, Critical Reviews in Neurobiology, V15, P41, DOI 10.1615/CritRevNeurobiol.v15.i1.20