Ryan P J, Krstew E V, Sarwar M, Gundlach A L, Lawrence A J
The Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia; Florey Department of Neuroscience and Mental Health, The University of Melbourne, Parkville, Victoria, Australia.
The Florey Institute of Neuroscience and Mental Health, Parkville, Victoria, Australia.
Drug Alcohol Depend. 2014 Jul 1;140:8-16. doi: 10.1016/j.drugalcdep.2014.04.017. Epub 2014 Apr 28.
Chronic alcohol intake produces multiple neuroadaptive changes, including up- and down-regulation of neuropeptides and receptors. There are widespread projections of relaxin-3 containing neurons to, and abundant relaxin family peptide 3 receptor (RXFP3) expression within, brain regions involved in modulating alcohol intake. Recently we demonstrated the involvement of relaxin-3/RXFP3 signalling in alcohol-seeking in rats; therefore in this study we examined whether relaxin-3 and/or RXFP3 expression were altered by chronic alcohol intake in alcohol-preferring iP rats.
Expression of relaxin-3 mRNA in the hindbrain nucleus incertus and RXFP3 radioligand binding levels in discrete forebrain regions were investigated following voluntary intake of alcohol or sucrose for 12 weeks, with a 2 day washout, using quantitative in situ hybridisation histochemistry and in vitro receptor autoradiography, respectively, in cohorts of adult, male iP rats.
Levels of relaxin-3 mRNA in the hindbrain nucleus incertus were positively correlated with the level of intake of both alcohol (r(12)=0.59, p=0.03) and sucrose (r(7)=0.70, p=0.04) in iP rats. Dense binding of the RXFP3-selective radioligand, [(125)]-R3/I5, was detected in hypothalamic and extrahypothalamic sites, but no significant changes in the density of RXFP3 were observed in the brain regions quantified following chronic sucrose or ethanol intake.
Our findings suggest high endogenous relaxin-3 expression may be associated with higher intake of rewarding substances, rather than its expression being regulated in response to their intake, consistent with an active role for the relaxin-3/RXFP3 system in modulating ingestive and alcohol-related behaviours.
长期饮酒会产生多种神经适应性变化,包括神经肽和受体的上调和下调。含松弛素-3的神经元广泛投射到参与调节酒精摄入的脑区,且这些脑区内有丰富的松弛素家族肽3受体(RXFP3)表达。最近我们证明了松弛素-3/RXFP3信号通路参与大鼠的觅酒行为;因此,在本研究中,我们检测了偏爱酒精的iP大鼠长期饮酒是否会改变松弛素-3和/或RXFP3的表达。
成年雄性iP大鼠自愿摄入酒精或蔗糖12周,随后有2天的洗脱期,分别使用定量原位杂交组织化学和体外受体放射自显影技术,研究成年雄性iP大鼠后脑不确定核中松弛素-3 mRNA的表达以及离散前脑区域中RXFP3放射性配体结合水平。
iP大鼠后脑不确定核中松弛素-3 mRNA水平与酒精(r(12)=0.59,p=0.03)和蔗糖(r(7)=0.70,p=0.04)的摄入量均呈正相关。在丘脑下部和下丘脑外部位检测到RXFP3选择性放射性配体[(125)]-R3/I5的密集结合,但在长期摄入蔗糖或乙醇后定量的脑区中未观察到RXFP3密度的显著变化。
我们的研究结果表明,内源性松弛素-3高表达可能与奖励性物质的高摄入量有关,而不是其表达受摄入量的调节,这与松弛素-3/RXFP3系统在调节摄食和酒精相关行为中的积极作用一致。