Chan-Palay V
Anat Embryol (Berl). 1975 Dec 31;148(3):235-65. doi: 10.1007/BF00319846.
The cerebellar cortex and deep cerebellar nuclei in rats and rhesus monkey were studied after treatment with monoamine oxidase inhibitor and continuous intraventricular infusion with 10(-5) M serotonin-3H. Autoradiographs were prepared for light and electron microscopy. The cerebellum contained no labelled cells. Labelled unmyelinated axons arrive from the brain stem via the periventricular zones of the aqueduct and fourth ventricle. In the parafloccular cortex about 1 per cent of the mossy fibers are labelled, together with a small number of fine varicose axons in the molecular layer that run parallel to the folial axes (less than 0.1%). In the paravermal and vermal cortex there are few labelled fibers in the granular layer and a five-fold greater number of labelled axons in the molecular layer (about 0.5%). Apparently three systems of serotonin-containing axons are present in the cortex: mossy fibers, parallel fiber-like, and a diffuse system in granular and molecular layers. The fastigial (medial), interpositus, and dentate (lateral) nuclei, lateral vestibular and other vestibular nuclei all have numerous labelled axons. The dentate and interpositus nuclei receive labelled fibers which arrive through the superior cerebellar peduncle as well as from the periventricular area. Six morphologically different classes of labelled axon terminals have been differentiated. Class 1a, the mossy fiber rosettes, and class 1b, the CAT2 axons, have small, round, clear synaptic vesicles and large granular vesicles (lgv); class 2 axons have a distinctive collection of round granular vesicles; class 3 boutons have numerous tubular profiles, a few containing dense dots, packed in a dark axoplasmic matrix; class 4 axons have tiny 250 A granular vesicles, clear tubular profiles and occasional LGV; class 5 terminals have numerous LGV, both round and elongated, with clear round and tubular profiles; class 6 terminals have LGV, clear and granular synaptic vesicles and clear tubular profiles. All these axons have LGV 900 A in diameter with 500-600 A variably dense centers that do not fill the vesicle, and Gray's type 1 axodendritic or axasomatic synapses on postsynaptic locations in the cortex and nuclei. Labelled axons in the cortex end as mossy fibers upon granule cell dendrites in glomeruli (Class 1a) or upon dendrites of cortical interneurons, e.g. Golgi cells, basket and stellate cells, and not on Purkinje cells. ...
在用单胺氧化酶抑制剂处理并持续脑室内注入10⁻⁵M 5-羟色胺-³H后,对大鼠和恒河猴的小脑皮质及小脑深部核团进行了研究。制备了用于光镜和电镜观察的放射自显影片。小脑中未发现标记细胞。标记的无髓轴突通过中脑导水管和第四脑室的室周区从脑干传入。在旁绒球皮质,约1%的苔藓纤维被标记,分子层还有少量与小叶轴平行的细的曲张轴突被标记(少于0.1%)。在小脑旁叶和蚓叶皮质,颗粒层中标记纤维很少,分子层中标记轴突数量多5倍(约0.5%)。显然,皮质中存在三种含5-羟色胺的轴突系统:苔藓纤维、平行纤维样以及颗粒层和分子层中的弥散系统。顶核(内侧)、间位核、齿状核(外侧)、外侧前庭核及其他前庭核均有大量标记轴突。齿状核和间位核接受通过小脑上脚以及从室周区传来的标记纤维。已区分出六种形态不同的标记轴突终末类型。1a类,即苔藓纤维花结,和1b类,即CAT2轴突,具有小的、圆形的、清亮的突触小泡和大的颗粒小泡(lgv);2类轴突有独特的圆形颗粒小泡集合;3类终扣有许多管状轮廓,少数含有致密小点,聚集在暗的轴浆基质中;4类轴突有微小的250埃颗粒小泡、清亮的管状轮廓和偶尔的lgv;5类终末有许多lgv,圆形和细长形都有,有清亮的圆形和管状轮廓;6类终末有lgv、清亮的和颗粒性突触小泡以及清亮的管状轮廓。所有这些轴突都有直径900埃的lgv,中心密度可变,为500 - 600埃,不充满小泡,在皮质和核的突触后部位形成格雷I型轴 - 树突或轴 - 体突触。皮质中的标记轴突以苔藓纤维形式终止于小球中的颗粒细胞树突上(1a类),或终止于皮质中间神经元的树突上,如高尔基细胞、篮状细胞和星状细胞,而不是终止于浦肯野细胞上。...