Reorganization of the peripheral projections of the trigeminal ganglion following neonatal transection of the infraorbital nerve.

R W Rhoades, N L Chiaia, R D Mooney, B G Klein, W E Renehan, M F Jacquin
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引用次数: 40

Abstract

Two different anatomical techniques were used to obtain evidence that transection of the infraorbital (IO) nerve on the day of birth would result in reorganization of the peripheral projections of the trigeminal nerve. In 14 of 19 neonatally nerve-damaged adult rats, injection of horseradish peroxidase (HRP) directly into the IO nerve, proximal to the point of the neonatal transection, resulted in labeled cells in the ophthalmic-maxillary portion of the ganglion and labeled fibers in mandibular sensory nerves. In an additional 28 neonatally nerve-damaged adult rats, double-labeling techniques were employed to document the reorganization suggested by the HRP tracing experiments. In these experiments, one fluorescent tracer, diamidino yellow (DY), was injected directly into the regenerate IO nerve, proximal to the point of the neonatal transection; a second tracer, true blue (TB), was deposited into peripheral ophthalmic and/or mandibular fields. These combinations of injections invariably resulted in the demonstration of a small number (46-401) of double-labeled cells that were located in the ophthalmic-maxillary part of the ganglion. Identical combinations of injections in normal adult rats and the intact sides of nerve-damaged animals never produced more than 6 double-labeled cells per ganglion. In two additional series of experiments, sequential double-labeling techniques were employed to demonstrate that the multiply projecting ganglion cells probably arose in at least two ways: (1) development of non-IO projections by ganglion cells that contributed axons to the IO nerve at the time of the lesion; (2) elaboration of IO axon branches by primary afferent neurons that had non-IO projections at the time of the lesion. A final two-stage double-labeling experiment demonstrated that approximately 75% of the ganglion cells that projected to the whisker pad at birth, and survived transection of the IO nerve on the first postnatal day, regenerated axons into this trigeminal branch.

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新生儿眶下神经横断后三叉神经节外周突起的重组。
我们采用两种不同的解剖技术来获得证据,证明出生当天眶下神经的横断会导致三叉神经周围投射的重组。将辣根过氧化物酶(HRP)直接注射到新生儿神经横断点近端的IO神经中,结果显示神经节眼颌部分有标记细胞,下颌骨感觉神经中有标记纤维。在另外28只新生神经损伤的成年大鼠中,采用双标记技术记录HRP示踪实验提示的重组。在这些实验中,一种荧光示踪剂,二氨基黄(DY),直接注射到再生IO神经,近端新生儿横断点;第二种示踪剂,真蓝(TB),沉积于眼周和/或下颌野。这些注射组合不可避免地导致少量(46-401)双标记细胞位于神经节的眼颌部。在正常成年大鼠和神经受损动物的完整侧进行相同的注射组合,每个神经节产生的双标记细胞从未超过6个。在另外两个系列的实验中,采用连续双标记技术证明了多个突出的神经节细胞可能至少以两种方式产生:(1)在病变发生时,神经节细胞向内IO神经提供轴突,从而形成非内IO神经突出;(2)损伤时具有非IO投射的初级传入神经元对IO轴突分支的细化。最后的两阶段双标记实验表明,大约75%的神经节细胞在出生时投射到须垫,并在出生后第一天横断IO神经后存活下来,在三叉神经分支再生轴突。
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