Gage F H, Chen K S, Buzsaki G, Armstrong D
University of California, San Diego, Department of Neurosciences, La Jolla 92093.
Neurobiol Aging. 1988 Sep-Dec;9(5-6):645-55. doi: 10.1016/s0197-4580(88)80129-5.
Rats exhibit morphological, biochemical, and metabolic changes in their brains, as well as cognitive deficits, with aging. Aged rats were found to be significantly impaired compared to young rats in a water maze task and test of motor coordination, and show reduced locomotor activity and exploration. Although aged rats did exhibit deficits as a group, not all aged rats were impaired. Additionally, the subgroup that was impaired on one task was not necessarily the subgroup that was impaired on another task. The cholinergic projection neurons in the basal forebrain region were significantly atrophied in the aged rodent. The degree of atrophy was highly correlated with the cognitive impairment exhibited on the Morris water maze task. Swollen choline acetyltransferase (ChAT)-positive "plaque-like" structures were observed in the neocortex of the aged but not the young rats. Declines in cholinergic activity in the brain has also been observed during aging. Biochemical measurements of ChAT in the basal forebrain region of aged rats revealed small but consistent decreases in ChAT activity compared to young rats. General metabolic activity, measured by the 2-deoxyglucose method, was also decreased in the hippocampal CA1 and CA3 fields, the dentate gyrus, the medial septal-diagonal band area, and the prefrontal cortex of aged rats. There was a significant correlation between the decrease in glucose utilization and deficits on the Morris water maze. Most aged rats exhibit pathological EEG patterns as reflected by frequent long-duration high voltage neocortical spindles (HVS) during immobility. Bilateral lesions of the nucleus basalis and scopolamine treatment increased the incidence of HVS, thereby mimicking changes in the aged brain. We attempted to ameliorate the cognitive deficits observed in subgroups or impaired rats by either: (1) implanting fetal cells of basal forebrain origin into the hippocampus, or (2) infusing nerve growth factor (NGF) chronically into the lateral ventricle. The grafts appeared to facilitate an improvement in the ability of the impaired aged rats to perform in the Morris water maze. This improved performance was reversed by injections of atropine at doses that did not affect the behavior of young animals that performed well in the same task. These results suggest that enhancement of the cholinergic system could have an effect on the performance of the impaired aged animals. The study of the effects of infusions of NGF clearly demonstrate that the ability of impaired aged rats to remember what they had previously learned was increased after NGF treatment.(ABSTRACT TRUNCATED AT 400 WORDS)
随着年龄增长,大鼠大脑会出现形态、生化及代谢变化,以及认知缺陷。与年轻大鼠相比,老年大鼠在水迷宫任务和运动协调测试中表现出明显受损,且运动活动和探索能力降低。虽然老年大鼠作为一个群体确实存在缺陷,但并非所有老年大鼠都有损伤。此外,在一项任务中受损的亚组不一定在另一项任务中也受损。老年啮齿动物基底前脑区域的胆碱能投射神经元明显萎缩。萎缩程度与在莫里斯水迷宫任务中表现出的认知障碍高度相关。在老年大鼠而非年轻大鼠的新皮层中观察到肿胀的胆碱乙酰转移酶(ChAT)阳性“斑块样”结构。衰老过程中还观察到大脑胆碱能活性下降。对老年大鼠基底前脑区域ChAT的生化测量显示,与年轻大鼠相比,ChAT活性有小幅但持续的下降。通过2-脱氧葡萄糖法测量,老年大鼠海马CA1和CA3区、齿状回、内侧隔-斜带区及前额叶皮质的一般代谢活性也降低。葡萄糖利用的减少与莫里斯水迷宫中的缺陷之间存在显著相关性。大多数老年大鼠在静止时表现出病理性脑电图模式,表现为频繁出现长时间的高电压新皮质纺锤波(HVS)。基底核双侧损伤和东莨菪碱处理会增加HVS的发生率,从而模拟老年大脑的变化。我们试图通过以下两种方法改善在亚组或受损大鼠中观察到的认知缺陷:(1)将源自基底前脑的胎儿细胞植入海马体,或(2)将神经生长因子(NGF)长期注入侧脑室。移植似乎有助于改善受损老年大鼠在莫里斯水迷宫中的表现能力。这种改善的表现可被注射阿托品逆转,而该剂量的阿托品对在同一任务中表现良好的年轻动物的行为没有影响。这些结果表明,增强胆碱能系统可能会对受损老年动物的表现产生影响。对注入NGF效果的研究清楚地表明,NGF治疗后,受损老年大鼠记住之前所学内容的能力有所提高。(摘要截断于400字)