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在猫和豚鼠听觉系统中用D-天冬氨酸对螺旋神经节和颗粒细胞进行选择性标记。

Selective labeling of spiral ganglion and granule cells with D-aspartate in the auditory system of cat and guinea pig.

作者信息

Oliver D L, Potashner S J, Jones D R, Morest D K

出版信息

J Neurosci. 1983 Mar;3(3):455-72. doi: 10.1523/JNEUROSCI.03-03-00455.1983.

Abstract

The present study sought to locate putative glutamatergic or aspartatergic pathways in the auditory system of cats and guinea pigs. We injected 0.06 to 3 mM D-[3H] aspartate (D-Asp) in the cochlear nucleus before preparation for light microscopic autoradiography. At short survival times (15 and 40 min) there was heavy labeling of astrocytic somata. Labeling patterns typical of cochlear nerve endings decorated neurons in the cochlear nucleus, e.g., cell bodies and dendritic trunks of octopus cells. Labeling patterns consistent with retrograde axonal transport by the parallel fibers of granule cells appeared in the molecular layer of the dorsal cochlear nucleus and in the external granular layer. Retrograde labeling of the cochlear nerve root fibers also occurred. Consistent with these results are companion biochemical findings on the rapidly dissected cochlear nuclei of guinea pigs. The dorsal, anteroventral, and posteroventral cochlear nuclei, each, evinced uptake of D-Asp. Subsequently, electrical stimulation of each nucleus released a portion of the accumulated amino acid. Most of this release probably came from synaptic endings. Another group of experiments compared autoradiographic localization of 0.06 to 3 mM D-Asp to that of horseradish peroxidase (HRP) 6 hr to 2 d after injections in the cochlear nucleus. Astroglial cell bodies were no longer labeled by D-Asp, but spiral ganglion cell bodies in the cochlea and granule cell bodies in the cochlear nucleus were. Perikarya of the periolivary and ventral cochlear nuclei projecting to the dorsal cochlear nucleus were labeled by HRP and not by D-Asp. Thus, comparisons with the HRP findings indicate that D-Asp labeling resulted from a selective retrograde transport. There was no evidence for a selective anterograde axonal transport. The present observations support the hypothesis that cochlear nerve fibers and granule cells may use L-glutamate and/or L-aspartate as a transmitter in the cochlear nucleus.

摘要

本研究旨在确定猫和豚鼠听觉系统中假定的谷氨酸能或天冬氨酸能通路。在制备用于光学显微镜放射自显影之前,我们将0.06至3 mM的D-[3H]天冬氨酸(D-Asp)注入耳蜗核。在短存活时间(15和40分钟)时,星形胶质细胞体有大量标记。耳蜗神经末梢典型的标记模式装饰了耳蜗核中的神经元,例如章鱼细胞的细胞体和树突干。与颗粒细胞平行纤维逆行轴突运输一致的标记模式出现在背侧耳蜗核的分子层和外颗粒层。耳蜗神经根纤维也出现了逆行标记。与这些结果一致的是对豚鼠快速解剖的耳蜗核的相关生化研究结果。背侧、前腹侧和后腹侧耳蜗核均显示有D-Asp摄取。随后,对每个核进行电刺激会释放一部分积累的氨基酸。这种释放大部分可能来自突触末梢。另一组实验比较了在耳蜗核注射0.06至3 mM D-Asp与辣根过氧化物酶(HRP)6小时至2天后的放射自显影定位。星形胶质细胞体不再被D-Asp标记,但耳蜗中的螺旋神经节细胞体和耳蜗核中的颗粒细胞体被标记。投射到背侧耳蜗核的橄榄周核和腹侧耳蜗核的核周体被HRP标记而未被D-Asp标记。因此,与HRP结果的比较表明,D-Asp标记是由选择性逆行运输导致的。没有证据表明存在选择性顺行轴突运输。目前的观察结果支持这样的假设,即耳蜗神经纤维和颗粒细胞可能在耳蜗核中使用L-谷氨酸和/或L-天冬氨酸作为神经递质。

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