Pregnenolone sulfate, dehydroepiandrosterone sulfate and allotetrahydrodeoxycorticosterone affect rapid tolerance to the hypothermic effect of ethanol

被引:7
作者
Barbosa, ADE [1 ]
Morato, GS [1 ]
机构
[1] Univ Fed Santa Catarina, Ctr Ciencias Biol, Dept Farmacol, BR-88015420 Florianopolis, SC, Brazil
关键词
alcohol; neurosteroids; hypothermia; mice;
D O I
10.1016/S0361-9230(02)00765-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Our previous study showed that the neurosteroids pregnenolone sulfate (PS) and epipregnanolone stimulated and blocked, respectively, the demonstration of chronic tolerance to the incoordinating effect of ethanol. The aim of the present study was to investigate the influence of three neurosteroids on the demonstration of tolerance to ethanol-induced hypothermia in mice using the rapid tolerance paradigm. The first experiment defined the doses of ethanol that did or did not induce rapid tolerance to ethanol-induced hypothermia. In the second, the influence of pretreatment of mice with PS (0.08 or 0.15 mg/kg, i.p.) or dehydroepiandrosterone sulfate (DHEAS; 0.15 or 0.20 mg/kg, i.p.) before ethanol (4.0 g/kg, i.p.) on rapid tolerance was studied. The third experiment examined the effect of allotetrahydrodeoxicorticosterone (ALLOT, 0.10 or 0.20 mg/kg, i.p.) before ethanol (4.0 g/kg, i.p.) on rapid tolerance. Results showed that pretreatment with PS or with DHEAS significantly facilitated the demonstration of rapid tolerance, whereas pretreatment with ALLOT interfered with the demonstration of tolerance to the hypothermic effect. (C) 2002 Elsevier Science Inc. All rights reserved.
引用
收藏
页码:99 / 105
页数:7
相关论文
共 62 条
[41]   NEUROSTEROIDS, VIA SIGMA-RECEPTORS, MODULATE THE [H-3] NOREPINEPHRINE RELEASE EVOKED BY N-METHYL-D-ASPARTATE IN THE RAT HIPPOCAMPUS [J].
MONNET, FP ;
MAHE, V ;
ROBEL, P ;
BAULIEU, EE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (09) :3774-3778
[42]   SELECTIVE IMPAIRMENT OF LEARNING AND BLOCKADE OF LONG-TERM POTENTIATION BY AN N-METHYL-D-ASPARTATE RECEPTOR ANTAGONIST, AP5 [J].
MORRIS, RGM ;
ANDERSON, E ;
LYNCH, GS ;
BAUDRY, M .
NATURE, 1986, 319 (6056) :774-776
[43]  
MORRISETT RA, 1993, J NEUROSCI, V13, P2264
[44]  
MORROW AL, 1988, J PHARMACOL EXP THER, V246, P158
[45]   Distinct sites for inverse modulation of N-methyl-D-aspartate receptors by sulfated steroids [J].
Park-Chung, M ;
Wu, FS ;
Purdy, RH ;
Malayev, AA ;
Gibbs, TT ;
Farb, DH .
MOLECULAR PHARMACOLOGY, 1997, 52 (06) :1113-1123
[46]   In vitro tolerance to inhibition by ethanol of N-methyl-D-aspartate-induced depolarization in locus coeruleus neurons of behaviorally ethanol-tolerant rats [J].
Poelchen, W ;
Kittner, H ;
Sieler, D ;
Regenthal, R ;
Preiss, R ;
Iles, P .
NEUROCHEMISTRY INTERNATIONAL, 2001, 39 (01) :51-58
[47]   DIFFERENTIAL ANTAGONISM BY EPIPREGNANOLONE OF ALPHAXALONE AND PREGNANOLONE POTENTIATION OF [H-3] FLUNITRAZEPAM BINDING SUGGESTS MORE THAN ONE CLASS OF BINDING-SITE FOR STEROIDS AT GABA-A RECEPTORS [J].
PRINCE, RJ ;
SIMMONDS, MA .
NEUROPHARMACOLOGY, 1993, 32 (01) :59-63
[48]   ACUTE ALCOHOL BLOCKS NEUROSTEROID MODULATION OF SYNAPTIC TRANSMISSION AND LONG-TERM POTENTIATION IN THE RAT HIPPOCAMPAL SLICE [J].
RANDALL, RD ;
LEE, SY ;
MEYER, JH ;
WITTENBERG, GF ;
GRUOL, DL .
BRAIN RESEARCH, 1995, 701 (1-2) :238-248
[49]   NEUROSTEROIDS - BIOSYNTHESIS AND FUNCTION [J].
ROBEL, P ;
BAULIEU, EE .
TRENDS IN ENDOCRINOLOGY AND METABOLISM, 1994, 5 (01) :1-8
[50]   Sensitivity and tolerance to ethanol-induced incoordination and hypothermia in HAFT and LAFT mice [J].
Rustay, NR ;
Boehm, SL ;
Schafer, GL ;
Browman, KE ;
Erwin, VG ;
Crabbe, JC .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2001, 70 (01) :167-174