Department of Anatomy, University of California, San Francisco, California 94143; email:
The Eli and Edythe Broad Center of Regeneration Medicine and Stem Cell Research, University of California, San Francisco, California 94143.
Annu Rev Neurosci. 2017 Jul 25;40:251-272. doi: 10.1146/annurev-neuro-072116-031357. Epub 2017 Apr 24.
The past two decades have seen remarkable progress in our understanding of the multifactorial drivers of hippocampal aging and cognitive decline. Recent findings have also raised the possibility of functional rejuvenation in the aged hippocampus. In this review, we aim to synthesize the mechanisms that drive hippocampal aging and evaluate critically the potential for rejuvenation. We discuss the functional changes in synaptic plasticity and regenerative potential of the aged hippocampus, followed by mechanisms of microglia aging, and assess the cross talk between these proaging processes. We then examine proyouth interventions that demonstrate significant promise in reversing age-related impairments in the hippocampus and, finally, attempt to look ahead toward novel therapeutics for brain aging.
在过去的二十年中,我们对海马体衰老和认知能力下降的多因素驱动因素有了显著的认识。最近的研究结果也提出了在老年海马体中实现功能复兴的可能性。在这篇综述中,我们旨在综合驱动海马体衰老的机制,并批判性地评估复兴的潜力。我们讨论了突触可塑性和衰老海马体再生潜力的功能变化,接着讨论了小胶质细胞衰老的机制,并评估了这些衰老过程之间的相互作用。然后,我们研究了一些有希望逆转海马体与年龄相关损伤的促进年轻干预措施,最后,试图展望针对大脑衰老的新型治疗方法。