Graham Danielle L, Edwards Scott, Bachtell Ryan K, DiLeone Ralph J, Rios Maribel, Self David W
Department of Psychiatry, The Seay Center for Basic and Applied Research in Psychiatric Illness, The University of Texas Southwestern Medical Center, Dallas, Texas 75390-9070, USA.
Nat Neurosci. 2007 Aug;10(8):1029-37. doi: 10.1038/nn1929. Epub 2007 Jul 8.
A single exposure to cocaine rapidly induces the brief activation of several immediate early genes, but the role of such short-term regulation in the enduring consequences of cocaine use is poorly understood. We found that 4 h of intravenous cocaine self-administration in rats induced a transient increase in brain-derived neurotrophic factor (BDNF) and activation of TrkB-mediated signaling in the nucleus accumbens (NAc). Augmenting this dynamic regulation with five daily NAc BDNF infusions caused enduring increases in cocaine self-administration, and facilitated relapse to cocaine seeking in withdrawal. In contrast, neutralizing endogenous BDNF regulation with intra-NAc infusions of antibody to BDNF subsequently reduced cocaine self-administration and attenuated relapse. Using localized inducible BDNF knockout in mice, we found that BDNF originating from NAc neurons was necessary for maintaining increased cocaine self-administration. These findings suggest that dynamic induction and release of BDNF from NAc neurons during cocaine use promotes the development and persistence of addictive behavior.
单次接触可卡因会迅速诱导多个即刻早期基因短暂激活,但这种短期调节在可卡因使用的持久后果中所起的作用却鲜为人知。我们发现,大鼠静脉注射可卡因自我给药4小时会导致脑源性神经营养因子(BDNF)短暂增加,并激活伏隔核(NAc)中TrkB介导的信号传导。通过每天向伏隔核注射五次BDNF来增强这种动态调节,会导致可卡因自我给药持续增加,并促进戒断后复吸可卡因。相反,通过向伏隔核内注射抗BDNF抗体来中和内源性BDNF调节,随后会减少可卡因自我给药并减轻复吸。利用小鼠局部诱导性BDNF基因敲除,我们发现源自伏隔核神经元的BDNF对于维持可卡因自我给药增加是必要的。这些发现表明,在使用可卡因期间,BDNF从伏隔核神经元的动态诱导和释放促进了成瘾行为的发展和持续。