Bloss Erik B, Hunter Richard G, Waters Elizabeth M, Munoz Carmen, Bernard Katie, McEwen Bruce S
The Laboratory of Neuroendocrinology, The Rockefeller University, New York, NY 10021, USA.
Exp Neurol. 2008 Mar;210(1):109-17. doi: 10.1016/j.expneurol.2007.10.007. Epub 2007 Oct 24.
AMPA receptors are a major subtype of ionotropic receptors that respond to glutamate. Positive allosteric modulators of AMPA receptors selectively enhance fast excitatory neurotransmission in the brain and increase overall neuronal excitability. In addition to enhancing cognitive performance, S18986 (Servier, France) and other AMPA receptor modulators have also been shown to be neuroprotective. A particularly relevant context for AMPAR modulator studies is during aging because of increased neuronal vulnerability. It is currently unknown if chronic AMPAR modulator treatment can alter the course of brain aging, a process characterized by impairment of cognitive function, reduced neuronal excitability, and increased inflammation in the brain. We examined the behavioral and some relevant CNS effects of chronic S18986 in rats from 14 to 18 months of age. Here we show that chronic, oral administration of S18986 increases locomotor activity and performance in a spatial memory task in aged rodents. In addition, chronic S18986 treatment retards the decline of forebrain cholinergic neurons by roughly 37% and midbrain dopaminergic neurons by as much as 43% during aging and attenuates the age-related increase in the expression of a microglial marker in the hippocampus. These results provide a framework for further studies of the potentially beneficial effects of AMPAR modulators on brain aging.
AMPA 受体是离子型受体的主要亚型,对谷氨酸有反应。AMPA 受体的正变构调节剂可选择性增强大脑中的快速兴奋性神经传递,并增加整体神经元兴奋性。除了增强认知能力外,S18986(法国施维雅公司)和其他 AMPA 受体调节剂也已被证明具有神经保护作用。由于神经元易损性增加,AMPA 受体调节剂研究的一个特别相关的背景是在衰老过程中。目前尚不清楚长期使用 AMPA 受体调节剂治疗是否能改变大脑衰老的进程,大脑衰老的特征是认知功能受损、神经元兴奋性降低和大脑炎症增加。我们研究了 14 至 18 月龄大鼠长期使用 S18986 的行为及一些相关的中枢神经系统效应。在此我们表明,长期口服 S18986 可增加老年啮齿动物的自发活动和空间记忆任务中的表现。此外,长期使用 S18986 治疗可使衰老过程中前脑胆碱能神经元的衰退延缓约 37%,中脑多巴胺能神经元的衰退延缓多达 43%,并减轻海马体中与年龄相关的小胶质细胞标志物表达增加。这些结果为进一步研究 AMPA 受体调节剂对大脑衰老的潜在有益作用提供了框架。