Redgrave P, Mitchell I
Neuroscience. 1982 Apr;7(4):871-83. doi: 10.1016/0306-4522(82)90048-3.
New procedure for quantitative photometric assessment of glyoxylic acid-induced fluorescence of dopamine in the caudate nucleus are presented. A recently published cryostat method was used to process a series of 24 micrometer sections taken from the caudate nucleus of each animal. Fluorescent light contained within a circular field (0.8 mm diameter) was measured photometrically. Several defined positions within the caudate nucleus on each tissue section were selected for measurement. Thus, a grid of measurements taken throughout the caudate nucleus provided a three-dimensional description of fluorescence intensity within this structure on both sides of the brain. Several experiments were performed to evaluate both the reliability and validity of these procedures as an index of the relative regional content of dopamine within the caudate: (1) the relative distribution of fluorescence intensity within the mouse striatum was in good agreement with previously reported distributions based on biochemical determination of regional dopamine levels within the rodent brain; (2) pharmacological manipulation of dopamine levels with gamma-butyrolactone and alpha-methyl-p-tyrosine combined with amphetamine produced predictable changes in the fluorescence intensity measurements of mouse caudate relative to untreated controls; (3) in rats pre-treated with alpha-methyl-p-tyrosine, unilateral electrical stimulation of the substantia nigra caused overall differences in fluorescence intensity between the caudate nucleus on each side of the brain, which were a function of both the duration of stimulation and the stimulating pulse frequency; (4) local injections of 6-hydroxydopamine unilaterally into the ventral tegmentum of animals pretreated with desmethylimipramine caused significant reductions in the intensity of fluorescence recorded from the ipsilateral striatum. It is concluded that the photometric procedures presented in this report constitute a significant improvement in the description of regional variations in the intensity of dopamine-related fluorescence in the caudate nucleus.
本文介绍了一种用于定量光度评估尾状核中乙醛酸诱导的多巴胺荧光的新方法。采用最近发表的低温恒温器方法处理从每只动物的尾状核获取的一系列24微米厚的切片。对直径为0.8毫米的圆形视野内的荧光进行光度测量。在每个组织切片的尾状核内选择几个特定位置进行测量。因此,在整个尾状核进行的测量网格提供了大脑两侧该结构内荧光强度的三维描述。进行了多项实验以评估这些程序作为尾状核内多巴胺相对区域含量指标的可靠性和有效性:(1)小鼠纹状体内荧光强度的相对分布与先前基于啮齿动物脑内区域多巴胺水平生化测定所报告的分布高度一致;(2)用γ-丁内酯和α-甲基-p-酪氨酸联合安非他命对多巴胺水平进行药理学操作,相对于未处理的对照,小鼠尾状核的荧光强度测量产生了可预测的变化;(3)在预先用α-甲基-p-酪氨酸处理的大鼠中,单侧电刺激黑质导致大脑两侧尾状核之间荧光强度的总体差异,这是刺激持续时间和刺激脉冲频率两者的函数;(4)对用去甲丙咪嗪预处理的动物单侧腹侧被盖区局部注射6-羟基多巴胺,导致同侧纹状体记录的荧光强度显著降低。结论是,本报告中提出的光度测量程序在描述尾状核中多巴胺相关荧光强度的区域变化方面有显著改进。