Russo Scott J, Mazei-Robison Michelle S, Ables Jessica L, Nestler Eric J
Fishberg Department of Neuroscience, Mount Sinai School of Medicine, One Gustave Levy Place, New York, NY 10029, USA.
Neuropharmacology. 2009;56 Suppl 1(Suppl 1):73-82. doi: 10.1016/j.neuropharm.2008.06.059. Epub 2008 Jul 4.
Drugs of abuse produce widespread effects on the structure and function of neurons throughout the brain's reward circuitry, and these changes are believed to underlie the long-lasting behavioral phenotypes that characterize addiction. Although the intracellular mechanisms regulating the structural plasticity of neurons are not fully understood, accumulating evidence suggests an essential role for neurotrophic factor signaling in the neuronal remodeling which occurs after chronic drug administration. Brain-derived neurotrophic factor (BDNF), a growth factor enriched in brain and highly regulated by several drugs of abuse, regulates the phosphatidylinositol 3'-kinase (PI3K), mitogen-activated protein kinase (MAPK), phospholipase Cgamma (PLCgamma), and nuclear factor kappa B (NFkappaB) signaling pathways, which influence a range of cellular functions including neuronal survival, growth, differentiation, and structure. This review discusses recent advances in our understanding of how BDNF and its signaling pathways regulate structural and behavioral plasticity in the context of drug addiction.
滥用药物会对整个大脑奖赏回路中神经元的结构和功能产生广泛影响,而这些变化被认为是成瘾所特有的持久行为表型的基础。尽管调节神经元结构可塑性的细胞内机制尚未完全明确,但越来越多的证据表明神经营养因子信号在慢性药物给药后发生的神经元重塑中起着至关重要的作用。脑源性神经营养因子(BDNF)是一种在大脑中富集且受多种滥用药物高度调节的生长因子,它调节磷脂酰肌醇3'-激酶(PI3K)、丝裂原活化蛋白激酶(MAPK)、磷脂酶Cγ(PLCγ)和核因子κB(NFκB)信号通路,这些信号通路影响一系列细胞功能,包括神经元的存活、生长、分化和结构。本综述讨论了我们在理解BDNF及其信号通路如何在药物成瘾背景下调节结构和行为可塑性方面的最新进展。