Scrable Heidi, Burns-Cusato Melissa, Medrano Silvia
Kogod Center on Aging, Mayo Clinic, Rochester, MN 55905, USA.
Biochim Biophys Acta. 2009 Dec;1790(12):1587-91. doi: 10.1016/j.bbagen.2009.09.007. Epub 2009 Oct 1.
We propose a model in which cell loss in the aging brain is seen as a root cause of behavioral changes that compromise quality of life, including the onset of generalized anxiety disorder, in elderly individuals. According to this model, as stem cells in neurogenic regions of the adult brain lose regenerative capacity, worn-out, dead, or damaged neurons fail to be replaced, leaving gaps in function. As most replacement involves inhibitory interneurons, either directly or indirectly, the net result is the acquisition over time of a hyper-excitable state. The stress axis is subserved by all three neurogenic regions in the adult brain, making it particularly susceptible to these age-dependent changes. We outline a molecular mechanism by which hyper-excitation of the stress axis in turn activates the tumor suppressor p53. This reinforces the loss of stem cell proliferative capacity and interferes with the feedback mechanism by which the glucocorticoid receptor turns off neuroendocrine pathways and resets the axis.
我们提出了一个模型,在该模型中,衰老大脑中的细胞损失被视为行为改变的根本原因,这些行为改变会损害老年人的生活质量,包括广泛性焦虑症的发作。根据这个模型,随着成人大脑神经源性区域的干细胞失去再生能力,磨损、死亡或受损的神经元无法被替换,从而导致功能出现缺口。由于大多数替换过程直接或间接地涉及抑制性中间神经元,最终结果是随着时间的推移会出现过度兴奋状态。应激轴由成人大脑中所有三个神经源性区域维持,这使得它特别容易受到这些与年龄相关的变化的影响。我们概述了一种分子机制,通过这种机制,应激轴的过度兴奋反过来会激活肿瘤抑制因子p53。这加剧了干细胞增殖能力的丧失,并干扰了糖皮质激素受体关闭神经内分泌途径并重置该轴的反馈机制。