Descarries L, Droz B
J Cell Biol. 1970 Feb;44(2):385-99. doi: 10.1083/jcb.44.2.385.
Catecholaminergic neurons, which take up and retain exogenous norepinephrine labeled with tritium, were studied by means of high resolution radioautography, in the substantia nigra, the substantia grisea periventricularis, and the locus coeruleus of the rat. Under the conditions required for the radioautographic detection of exogenous norepinephrine-(3)H, it was established that (1) glutaraldehyde was the most suitable fixative for preserving the labeled amine in situ; (2) norepinephrine-(3)H itself, rather than metabolites, accounted for most of the reactions detected in catecholaminergic neurons. At various time intervals after an intraventricular injection of norepinephrine-(3)H, the tracer reached a concentration 15-100 times higher, and disappeared at a slower rate, in presynaptic axons (t(1/2):4 hr) than in nerve cell bodies (t(1/2):0.8-1.3 hr). After pretreatment with a monoamine oxidase inhibitor, the radioautographic reactions increased and persisted longer, especially in the preterminal axons. Within neurons, the labeled amine was ubiquitously distributed in the nerve cell body and concentrated in presynaptic axons and synaptic terminals of various morphological types. Although large granular vesicles were usually present in the labeled axonal bulbs, no structural characteristic could be specifically ascribed to catecholaminergic neurons. It is suggested that exogenous norepinephrine bound to macromolecular complexes is present in all parts of catecholaminergic neurons and mainly concentrated within presynaptic axons.
采用高分辨率放射自显影术,对摄取并保留用氚标记的外源性去甲肾上腺素的儿茶酚胺能神经元进行了研究,研究对象为大鼠的黑质、室周灰质和蓝斑。在放射自显影检测外源性去甲肾上腺素-(3)H所需的条件下,确定了:(1)戊二醛是原位保存标记胺最合适的固定剂;(2)儿茶酚胺能神经元中检测到的大多数反应是由去甲肾上腺素-(3)H本身而非其代谢产物引起的。脑室内注射去甲肾上腺素-(3)H后的不同时间间隔,示踪剂在突触前轴突(半衰期:4小时)中的浓度比在神经细胞体(半衰期:0.8 - 1.3小时)中高15 - 100倍,且消失速度较慢。用单胺氧化酶抑制剂预处理后,放射自显影反应增强且持续时间更长,尤其是在终末前轴突中。在神经元内,标记胺广泛分布于神经细胞体,并集中在各种形态类型的突触前轴突和突触终末。虽然标记的轴突小球中通常存在大颗粒囊泡,但儿茶酚胺能神经元没有可明确归因的结构特征。提示与大分子复合物结合的外源性去甲肾上腺素存在于儿茶酚胺能神经元的所有部位,且主要集中在突触前轴突内。