Estradiol enhances ethanol reward in female mice through activation of ERα and ERβ

被引:26
|
作者
Hilderbrand, Elisa R. [1 ,2 ]
Lasek, Amy W. [2 ]
机构
[1] Univ Illinois, Grad Program Neurosci, 1601 West Taylor St,MC 912, Chicago, IL 60612 USA
[2] Univ Illinois, Dept Psychiat, Ctr Alcohol Res Epigenet, 1601 West Taylor St,MC 912, Chicago, IL 60612 USA
基金
美国国家卫生研究院;
关键词
Addiction; Alcohol; Estrogen; Female; Reward; CONDITIONED PLACE PREFERENCE; ESTROGEN-RECEPTOR-BETA; SEX-DIFFERENCES; OVARIECTOMIZED MICE; ALCOHOL-CONSUMPTION; SELECTIVE LIGANDS; SUBSTANCE-ABUSE; UNITED-STATES; C57BL/6J MICE; RATS;
D O I
10.1016/j.yhbeh.2018.01.001
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Alcohol use disorder (AUD) manifests differently in men and women, but little is known about sex differences in the brain's response to ethanol. It is known that the steroid hormone 17 beta-estradiol (E2) regulates voluntary ethanol consumption in female rodents. However, the role of E2 as a regulator of ethanol reward has not been investigated. In this study, we tested for the effects of E2 and agonists selective for the classical estrogen receptors, ER alpha and ER beta, on ethanol reward in ovariectomized (OVX) mice using the conditioned place preference (CPP) test. E2 enhanced ethanol CPP and, while specific activation of either receptor alone had no effect, co activation of ER alpha and ER beta also enhanced ethanol CPP, suggesting that E2 enhances ethanol reward in female mice through actions at both ERa and ER beta. These results have implications for sex differences in the development of AUD, suggesting that women may find ethanol more rewarding than men because of higher circulating E2 levels.
引用
收藏
页码:159 / 164
页数:6
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