Logrip Marian L, Janak Patricia H, Ron Dorit
Ernest Gallo Research Center, Emeryville, CA 94608, USA.
FASEB J. 2008 Jul;22(7):2393-404. doi: 10.1096/fj.07-099135. Epub 2008 Feb 29.
We recently identified brain-derived neurotrophic factor (BDNF) in the dorsal striatum to be a major component of a homeostatic pathway controlling ethanol consumption. We hypothesized that ethanol-mediated activation of the BDNF signaling cascade is required for the ethanol-related function of the neurotrophic factor. Here, we demonstrate that exposure of striatal neurons to ethanol results in the activation of the BDNF receptor TrkB, leading to the activation of the mitogen-activated protein kinase (MAP kinase) signaling pathway and the subsequent increase in the expression of preprodynorphin (Pdyn) via BDNF. Finally, we show that activation of the dynorphin receptor, the kappa opioid receptor (KOR), is required for the BDNF-mediated decrease in ethanol intake, illustrating a function of dynorphin in BDNF's homeostatic control of ethanol consumption. Taken together, these results demonstrate that BDNF regulates ethanol intake by initiation of MAP kinase signaling and the ensuing production of downstream gene products, including Pdyn.
我们最近发现,背侧纹状体中的脑源性神经营养因子(BDNF)是控制乙醇摄入的稳态途径的主要组成部分。我们假设,神经营养因子与乙醇相关的功能需要乙醇介导的BDNF信号级联激活。在此,我们证明,将纹状体神经元暴露于乙醇会导致BDNF受体TrkB激活,进而激活丝裂原活化蛋白激酶(MAP激酶)信号通路,并随后通过BDNF增加前强啡肽原(Pdyn)的表达。最后,我们表明,强啡肽受体(κ阿片受体,KOR)的激活是BDNF介导的乙醇摄入量减少所必需的,这说明了强啡肽在BDNF对乙醇摄入的稳态控制中的作用。综上所述,这些结果表明,BDNF通过启动MAP激酶信号传导以及随后产生包括Pdyn在内的下游基因产物来调节乙醇摄入。