Lucchi M L, Barazzoni A M, Clavenzani P, Chiocchetti R, Berardinelli P, Bortolami R
Department of Veterinary Morphophysiology and Animal Productions, University of Bologna, Italy.
Anat Rec. 1999 Apr 1;254(4):490-5. doi: 10.1002/(SICI)1097-0185(19990401)254:4<490::AID-AR4>3.0.CO;2-Z.
The fluorescent retrograde double labeling technique has been used to identify within the extraocular motor nuclei of the sheep the neurons projecting to the cerebellum and to provide evidence whether they are motor neurons sending collaterals to the cerebellum or a separate population of neurons. The study was performed on eight sheep. The fluorescent tracers used were Fast Blue and the diamidino yellow dihydrochloride. In one and the same animal a fluorescent tracer was injected into the extraocular muscles (EOMs) and the other into bilateral points of the vermal folia II-V and paramedian lobule, or into the vermal folia VI, VIIA and VIIB, or into the underlying fastigial nuclei. Within the oculomotor, trochlear, and abducens nuclei, almost all of the motor neurons were labeled by the tracer injected into the EOMs and only a few cells were fluorescent for the tracer infiltrated into the cerebellum. These latter labelings were present bilaterally, and their number and distribution did not show apparent differences after injecting the paramedian lobule and the vermal folia or the fastigial nucleus. Along the rostrocaudal extent of the oculomotor and trochlear nuclei, the neurons projecting to the cerebellum were intermingled with the motor neurons located in the nuclear area facing the medial longitudinal fasciculus. In the abducens nucleus they were restricted to the caudal pole of the nucleus, which is located ventrolaterally to the genu of the facial nerve. Double-labeled neurons were never found. The absence of double-labeled cells, in spite of the efficiency of the tracer infiltration into the EOMs and into the cerebellum, demonstrates that the cerebellar projections from the extraocular motor nuclei are not collaterals of the motor neurons, but axons of a separate population of neurons.
荧光逆行双重标记技术已被用于在绵羊的眼外肌运动核内识别投射到小脑的神经元,并提供证据证明它们是向小脑发送侧支的运动神经元,还是另一类独立的神经元群体。该研究对八只绵羊进行。使用的荧光示踪剂是快蓝和二盐酸双脒基黄。在同一只动物中,一种荧光示踪剂被注入眼外肌,另一种被注入小脑蚓部II-V叶和旁正中小叶的双侧点,或注入小脑蚓部VI、VIIA和VIIB叶,或注入其下方的顶核。在动眼神经核、滑车神经核和展神经核内,几乎所有的运动神经元都被注入眼外肌的示踪剂标记,而只有少数细胞对注入小脑的示踪剂呈荧光反应。后一种标记双侧出现,并在注入旁正中小叶、小脑蚓叶或顶核后,其数量和分布没有明显差异。在动眼神经核和滑车神经核的前后范围内,投射到小脑的神经元与位于面对内侧纵束的核区域内的运动神经元相互交织。在展神经核中,它们局限于核的尾极,该尾极位于面神经膝的腹外侧。从未发现双标记神经元。尽管示踪剂有效地渗入了眼外肌和小脑,但未发现双标记细胞,这表明眼外肌运动核向小脑的投射不是运动神经元的侧支,而是另一类独立神经元群体的轴突。