Sexually dimorphic role of BNST vasopressin cells in sickness and social behavior in male and female mice

被引:27
作者
Whylings, Jack [1 ]
Rigney, Nicole [1 ]
Peters, Nicole V. [1 ]
de Vries, Geert J. [1 ,2 ]
Petrulis, Aras [1 ]
机构
[1] Georgia State Univ, Neurosci Inst, 100 Piedmont Ave SE, Atlanta, GA 30303 USA
[2] Georgia State Univ, Dept Biol, 100 Piedmont Ave SE, Atlanta, GA 30303 USA
基金
美国国家卫生研究院;
关键词
Arginine vasopressin; Sickness behavior; Social behavior; Bed nucleus of the stria terminalis; MEDIAL AMYGDALOID NUCLEUS; TO-BRAIN COMMUNICATION; BED NUCLEUS; ARGININE-VASOPRESSIN; STRIA TERMINALIS; GALANIN NEURONS; LIPOPOLYSACCHARIDE; RECOGNITION; SEX; INFLAMMATION;
D O I
10.1016/j.bbi.2019.09.015
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Circumstantial evidence supports the hypothesis that the sexually dimorphic vasopressin (AVP) innervation of the brain tempers sickness behavior in males. Here we test this hypothesis directly, by comparing sickness behavior in animals with or without ablations of BNST AVP cells, a major source of sexually dimorphic AVP in the brain. We treated male and female AVP-iCre + and AVP-iCre - mice that had been injected with viral Cre-dependent caspase-3 executioner construct into the BNST with lipopolysaccharide (LPS) or sterile saline, followed by behavioral analysis. In all groups, LPS treatment reliably reduced motor behavior, increased anxiety-related behavior, and reduced sucrose preference and consumption. Male mice, whose BNST AVP cells had been ablated (AVP-iCre + ), displayed only minor reductions in LPS-induced sickness behavior, whereas their female counterparts displayed, if anything, an increase in sickness behaviors. All saline-treated mice with BNST AVP cell ablations consumed more sucrose than did control mice, and males, but not females, with BNST AVP cell ablations showed reduced preference for novel conspecifics compared to control mice. These data confirm that BNST AVP cells control social behavior in a sexually dimorphic way, but do not play a critical role in altering sickness behavior.
引用
收藏
页码:68 / 77
页数:10
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