Parent A, Smith Y
Département d'Anatomie, Faculté de Médecine, Université Laval, Quebec, Canada.
Brain Res. 1987 Dec 15;436(2):296-310. doi: 10.1016/0006-8993(87)91674-x.
The cellular origin and degree of collateralization of the subthalamostriatal, subthalamonigral and subthalamopallidal projections in the squirrel monkey (Saimiri sciureus) were studied using lectin-conjugated horseradish peroxidase (WGA-HRP), Nuclear yellow (NY) and Fast blue (FB) as retrograde tracers. In a first experimental group, WGA-HRP was injected in the left putamen and the right caudate nucleus. Following these injections numerous retrogradely labeled neurons occurred in the dorsolateral two-thirds of the subthalamic nucleus on the putamen-injected side, whereas a smaller number of positive cells were found in the ventromedial third of the same nucleus on the caudate-injected side. In a second experimental group NY was injected in the putamen whereas FB was delivered in the substantia nigra on the same side of the brain. After putaminonigral injections subthalamic cells containing the tracer injected in the putamen (about 75-80% of all retrogradely labeled neurons) occurred in the dorsolateral two-thirds of the nucleus, whereas those containing the tracer injected in the substantia nigra (about 20-25% of all positive subthalamic cells) were confined to the ventromedial third of the structure. Approximately 5-10% of all subthalamic positive neurons were double-labeled following putaminonigral injections. In a third experimental group, NY was injected in the caudate nucleus and FB in the substantia nigra on the same side. After such injections cells retrogradely labeled with NY or FB were present in about equal number and appeared closely intermingled in the ventromedial third of the subthalamic nucleus. Less than 10% of all positive subthalamic neurons were double-labeled following caudatonigral injections. In a fourth experimental group, NY was delivered in the globus pallidus and FB in the substantia nigra on the same side. In these animal cells containing the tracer delivered in the pallidum were about 4 times more numerous than those labeled with the tracer injected in the substantia nigra, and approximately 10-20% of all positive subthalamic neurons were double-labeled following pallidonigral injections. Most of these double-labeled cells occurred in the zone where the two populations of single-labeled cells overlapped. Finally, in a last experimental group, NY was injected in the pedunculopontine nucleus on one side and in the substantia nigra on the other. Following these injections cells containing the tracer delivered in the pedunculopontine nucleus were found to be 5-6 times less numerous than those labeled after substantia nigra injections...
利用凝集素结合辣根过氧化物酶(WGA-HRP)、核黄(NY)和快蓝(FB)作为逆行示踪剂,研究了松鼠猴(Saimiri sciureus)丘脑底核至纹状体、丘脑底核至黑质以及丘脑底核至苍白球投射的细胞起源和侧支化程度。在第一个实验组中,将WGA-HRP注入左侧壳核和右侧尾状核。注射后,在注入壳核一侧的丘脑底核背外侧三分之二区域出现大量逆行标记神经元,而在注入尾状核一侧的同一核团腹内侧三分之一区域发现的阳性细胞数量较少。在第二个实验组中,将NY注入壳核,而将FB注入大脑同一侧的黑质。壳核-黑质注射后,含有注入壳核示踪剂的丘脑底核细胞(约占所有逆行标记神经元的75-80%)出现在核团的背外侧三分之二区域,而含有注入黑质示踪剂的细胞(约占所有阳性丘脑底核细胞的20-25%)局限于该结构的腹内侧三分之一区域。壳核-黑质注射后,所有丘脑底核阳性神经元中约5-10%为双标记。在第三个实验组中,将NY注入尾状核,将FB注入大脑同一侧的黑质。注射后,用NY或FB逆行标记的细胞数量大致相等,且在丘脑底核腹内侧三分之一区域紧密混合出现。尾状核-黑质注射后,所有阳性丘脑底核神经元中不到10%为双标记。在第四个实验组中,将NY注入苍白球,将FB注入大脑同一侧的黑质。在这些动物中,含有注入苍白球示踪剂的细胞数量比注入黑质示踪剂标记的细胞多约4倍,苍白球-黑质注射后,所有阳性丘脑底核神经元中约10-20%为双标记。这些双标记细胞大多出现在两个单标记细胞群体重叠的区域。最后,在最后一个实验组中,将NY注入一侧的脚桥核,将FB注入另一侧的黑质。注射后,发现含有注入脚桥核示踪剂的细胞数量比黑质注射后标记的细胞少5-6倍……