Eisch Amelia J, Harburg Gwyndolen C
Department of Psychiatry, University of Texas Southwestern Medical Center, Dallas, Texas 75390-9070, USA.
Hippocampus. 2006;16(3):271-86. doi: 10.1002/hipo.20161.
Once thought to produce global, nonspecific brain injury, drugs of abuse are now known to produce selective neuro-adaptations in particular brain regions. These neuro-adaptations are being closely examined for clues to the development, maintenance, and treatment of addiction. The hippocampus is an area of particular interest, as it is central to many aspects of the addictive process, including relapse to drug taking. A recently appreciated hippocampal neuro-adaptation produced by drugs as diverse as opiates and psychostimulants is decreased neurogenesis in the sub-granular zone (SGZ). While the role of adult-generated neurons is not clear, their functional integration into hippocampal circuitry raises the possibility that decreased adult SGZ neurogenesis may alter hippocampal function in such a way as to maintain addictive behavior or contribute to relapse. Here, we review the impact of opiates and psychostimulants on the different stages of cell development in the adult brain, as well as the different stages of the addictive process. We discuss how examination of drug-induced alterations of adult neurogenesis advances our understanding of the complex mechanisms by which opiates and psychostimulants affect brain function while also opening avenues for novel ways of assessing the functional role of adult-generated neurons. In addition, we highlight key discrepancies in the field and underscore the necessity to move "beyond BrdU"--beyond merely counting new hippocampal cells labeled with the S phase marker bromodeoxyuridine--so as to probe mechanistic questions about how drug-induced alterations in adult hippocampal neurogenesis occur and what the functional ramifications of alterations in neurogenesis are for addiction.
曾经被认为会导致全身性、非特异性脑损伤的滥用药物,如今已知会在特定脑区产生选择性神经适应性变化。目前正在对这些神经适应性变化进行深入研究,以寻找成瘾发展、维持及治疗方面的线索。海马体是一个特别受关注的区域,因为它在成瘾过程的许多方面都起着核心作用,包括复吸。最近发现,诸如阿片类药物和精神兴奋剂等多种药物会导致海马体颗粒下区(SGZ)神经发生减少,这是一种新认识到的海马体神经适应性变化。虽然成年后生成的神经元的作用尚不清楚,但它们功能整合到海马体神经回路中,这增加了一种可能性,即成年SGZ神经发生减少可能会改变海马体功能,从而维持成瘾行为或导致复吸。在这里,我们回顾了阿片类药物和精神兴奋剂对成人大脑细胞发育不同阶段以及成瘾过程不同阶段的影响。我们讨论了对药物诱导的成年神经发生变化的研究如何增进我们对阿片类药物和精神兴奋剂影响脑功能的复杂机制的理解,同时也为评估成年后生成的神经元的功能作用开辟了新途径。此外,我们强调了该领域的关键差异,并强调有必要“超越BrdU”——不仅仅是计算用S期标记物溴脱氧尿苷标记的新海马体细胞——以便探究关于药物诱导的成年海马体神经发生变化如何发生以及神经发生变化对成瘾的功能影响的机制问题。