Increased alcohol consumption in relaxin-3 deficient male mice

被引:12
|
作者
Shirahase, Takahira [1 ,2 ]
Aoki, Miku [1 ,2 ]
Watanabe, Ryuji [1 ]
Watanabe, Yoshihisa [1 ]
Tanaka, Masaki [1 ]
机构
[1] Kyoto Prefectural Univ Med, Dept Basic Geriatr, Kamikyo Ku, Kyoto 6028566, Japan
[2] Kyoto Prefectural Univ Med, Dept Dent Med, Kamikyo Ku, Kyoto 6028566, Japan
基金
日本学术振兴会;
关键词
Relaxin-3; Alcohol; Knockout; Mouse; CORTICOTROPIN-RELEASING-FACTOR; ANXIETY-LIKE BEHAVIOR; NUCLEUS-INCERTUS; DEPENDENT RATS; MESSENGER-RNA; FOOD-INTAKE; NEURONS; DRINKING; STRESS; BRAIN;
D O I
10.1016/j.neulet.2015.12.014
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Relaxin-3 is a neuropeptide expressed in the brainstem, and predominantly localized in the gray matter of the midline dorsal pons termed the nucleus incertus. Relaxin-3-expressing neurons densely project axons rostrally to various forebrain regions including the septum, hippocampus, and lateral hypothalamus. Several relaxin-3 functions have been reported including food intake, stress responses, neuroendocrine function, emotion, and spatial memory. In addition, recently relaxin-3 and its receptor, RXFP3, were shown to regulate alcohol intake using an RXFP3 antagonist and RXFP3 gene knockout mice. In the present study, we investigated alcohol consumption in relaxin-3 knockout mice, and found that male but not female mice significantly drank more alcohol than wild-type mice in the two-bottle choice test. However, after chronic alcohol vapor exposure, wild-type and mutant mice did not show this difference in alcohol intake, although both genotypes exhibited increased alcohol consumption compared with non alcohol-exposed control mice. There was no genotype difference in sucrose or quinine preference. These results suggest that the relaxin-3 neuronal system modestly affects alcohol preference and consumption. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:155 / 160
页数:6
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