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仓鼠视网膜中的NADPH黄递酶神经元。

NADPH-diaphorase neurons in the retina of the hamster.

作者信息

Lau K C, So K F, Tay D, Leung M C

机构信息

Department of Anatomy, Faculty of Medicine, University of Hong Kong.

出版信息

J Comp Neurol. 1994 Dec 22;350(4):550-8. doi: 10.1002/cne.903500404.

Abstract

NADPH-diaphorase-positive neurons have been demonstrated in the inner nuclear layer and ganglion cell layer of the retina of different mammalian species, but so far no experiments have been conducted to identify whether these cells are amacrine cells and/or retinal ganglion cells. We attempted to solve this problem by studying the NADPH-diaphorase-positive neurons in the hamster retina. From the NADPH-diaphorase histochemical reaction, two distinct types of neurons in the hamster retina were identified. They were named ND(g) and ND(i) cells. The ND(g) cells were cells with larger somata, ranging from 10 to 21 microns in diameter with a mean of 15.58 microns (S.D. = 2.59). They were found in the ganglion cell layer only. The ND(i) cells were smaller, with the somata ranging from 7 to 11 microns and having the mean diameter of 8.77 microns (S.D. = 1.24). Most of the ND(i) cells were found in the inner nuclear layer, and only very few could be observed in the inner plexiform layer. On average, there were 8,033 ND(g) and 5,051 ND(i) cells in the ganglion cell layer and inner nuclear layer, respectively. Two experiments were performed to clarify whether any of the NADPH-diaphorase neurons were retinal ganglion cells. Following unilateral optic nerve section, which leads to the retrograde degeneration of retinal ganglion cells, the numbers of both ND(g) and ND(i) cells did not change significantly for up to 4 months. In addition, when retinal ganglion cells were prelabeled retrogradely (horseradish peroxidase or fluorescent microspheres) and retinas were then stained for NADPH diaphorase, no double-labeled neurons were detected. These results indicated that the NADPH-diaphorase neurons in the hamster retina were the amacrine cells in the inner nuclear layer and displaced amacrine cells in the ganglion cell layer. Dendrites of the ND(g) and ND(i) cells were found to stratify in sublaminae 1, 3, and 5 of the inner plexiform layer, with a prominent staining in the sublamina 5. The possible importance of this arrangement in the rod pathway is also discussed.

摘要

在不同哺乳动物物种的视网膜内核层和神经节细胞层中已证实存在NADPH黄递酶阳性神经元,但迄今为止尚未进行实验来确定这些细胞是否为无长突细胞和/或视网膜神经节细胞。我们试图通过研究仓鼠视网膜中的NADPH黄递酶阳性神经元来解决这个问题。从NADPH黄递酶组织化学反应中,在仓鼠视网膜中鉴定出两种不同类型的神经元。它们被命名为ND(g)和ND(i)细胞。ND(g)细胞是胞体较大的细胞,直径范围为10至21微米,平均为15.58微米(标准差 = 2.59)。它们仅在神经节细胞层中发现。ND(i)细胞较小,胞体范围为7至11微米,平均直径为8.77微米(标准差 = 1.24)。大多数ND(i)细胞在内核层中发现,仅在内部神经丛层中能观察到极少数。平均而言,神经节细胞层和内核层中分别有8033个ND(g)细胞和5051个ND(i)细胞。进行了两项实验以阐明是否有任何NADPH黄递酶神经元是视网膜神经节细胞。单侧视神经切断后,这会导致视网膜神经节细胞逆行变性,在长达4个月的时间里ND(g)和ND(i)细胞的数量均未发生显著变化。此外,当视网膜神经节细胞被逆行预标记(辣根过氧化物酶或荧光微球),然后对视网膜进行NADPH黄递酶染色时,未检测到双标记神经元。这些结果表明,仓鼠视网膜中的NADPH黄递酶神经元是内核层中的无长突细胞和神经节细胞层中的移位无长突细胞。发现ND(g)和ND(i)细胞的树突在内侧神经丛层的1、3和5亚层中分层,在5亚层中有明显的染色。还讨论了这种排列在视杆通路中的可能重要性。

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