Gerhardt G A, Maloney R E
Departments of Psychiatry and Pharmacology, Neuroscience Training Program, and Rocky Mountain Center for Sensor Technology, University of Colorado Health Sciences Center, Denver, CO 80262, USA.
Brain Res. 1999 Jan 16;816(1):68-77. doi: 10.1016/s0006-8993(98)01095-6.
The technique of intracranial microdialysis was used to investigate the effects of aging on the striatal dopaminergic system of the anesthetized Fischer 344 rat. Microdialysis probes were implanted into the striatum of young (2-8 months) and aged (24-28 months) urethane anesthetized rats. Striatal dialysate levels were analyzed for dopamine (DA), dihydroxyphenylacetic acid (DOPAC), homovanillic acid (HVA), 5-hydroxyindoleacetic acid (5-HIAA), and serotonin (5-HT) by high performance liquid chromatography with electrochemical detection. As compared to the young animals, basal extracellular levels of DA and DOPAC were significantly decreased in two groups of aged animals. Stimulation with excess potassium added through the microdialysis probe produced a robust overflow of DA in the young and aged rat striatum, but the evoked overflow of DA was not diminished in the aged rat striatum as compared to young animals. In contrast, d-amphetamine-evoked overflow of DA was again robust in young and aged animals, but was greatly decreased in the aged rat striatum as compared to the signals recorded in the young rats. Taken together with previous reports, these data support the hypothesis that a major change in the regulation of DA release that occurs in aging involves changes in the function of the neuronal uptake of DA, which may be a compensatory property of DA neurons in senescence.
采用颅内微透析技术研究衰老对麻醉的Fischer 344大鼠纹状体多巴胺能系统的影响。将微透析探针植入年轻(2 - 8个月)和老年(24 - 28个月)的乌拉坦麻醉大鼠的纹状体中。通过高效液相色谱 - 电化学检测法分析纹状体透析液中多巴胺(DA)、二羟基苯乙酸(DOPAC)、高香草酸(HVA)、5 - 羟吲哚乙酸(5 - HIAA)和5 - 羟色胺(5 - HT)的水平。与年轻动物相比,两组老年动物的DA和DOPAC基础细胞外水平显著降低。通过微透析探针添加过量钾进行刺激,在年轻和老年大鼠纹状体中均产生了强烈的DA溢出,但与年轻动物相比,老年大鼠纹状体中诱发的DA溢出并未减少。相反,d - 苯丙胺诱发的DA溢出在年轻和老年动物中同样强烈,但与年轻大鼠记录的信号相比,老年大鼠纹状体中的溢出大大减少。与先前的报道一起,这些数据支持这样的假设,即衰老过程中发生的DA释放调节的主要变化涉及DA神经元摄取功能的改变,这可能是衰老过程中DA神经元的一种代偿特性。