Takeda T, Maekawa K
Department of Physiology, Jichi Medical School, Tochigi-ken, Japan.
Exp Brain Res. 1989;76(2):323-32. doi: 10.1007/BF00247892.
The previous electrophysiological study reported that some of the Purkinje cells in the vestibulocerebellum were innervated by branching climbing fibers. To identify the cells of origin of these branching climbing fibers, a pair of retrograde fluorescent tracers, propidium iodide in combination with 4', 6-diamidino-2-phenylindole or diamidino yellow, were injected into two sites in the flocculus, nodulus and uvula. Proportions of double labeled neurons out of all labeled neurons in each subdivision of the contralateral inferior olive were studied. In cases of injections into the flocculus and nodulus, 13% (maximum 27%) of all the labeled neurons in the dorsal cap and 6% (maximum 12%) in the ventrolateral outgrowth were double labeled. In cases of injections into the nodulus and uvula, 20% neurons (maximum 34%) of the labeled neurons in the dorsal cap and 8% of those in the nucleus beta were double labeled. The present retrograde labeling study revealed that some dorsal cap neurons project to the uvula, which has not been reported previously in the rabbit. Injections into the flocculus and uvula caused only slight double labeling (0.4%) in the inferior olive.
先前的电生理研究报告称,前庭小脑的一些浦肯野细胞由分支攀缘纤维支配。为了确定这些分支攀缘纤维的起源细胞,将一对逆行荧光示踪剂,碘化丙啶与4',6-二脒基-2-苯基吲哚或二脒基黄组合,注射到绒球、小结和蚓垂的两个部位。研究了对侧下橄榄核各亚区中所有标记神经元中双重标记神经元的比例。在注射到绒球和小结的情况下,背帽中所有标记神经元的13%(最大27%)和腹外侧突出部中6%(最大12%)为双重标记。在注射到小结和蚓垂的情况下,背帽中标记神经元的20%(最大34%)和β核中8%的神经元为双重标记。目前的逆行标记研究表明,一些背帽神经元投射到蚓垂,这在兔子中以前尚未见报道。注射到绒球和蚓垂在下橄榄核中仅引起轻微的双重标记(0.4%)。