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大鼠视网膜中NADPH-黄递酶/一氧化氮合酶的定位:一项电子显微镜研究

Localization of NADPH-diaphorase/nitric oxide synthase in the rat retina: an electron microscopic study.

作者信息

Darius S, Wolf G, Huang P L, Fishman M C

机构信息

Institute of Medical Neurobiology, University of Magdeburg, Germany.

出版信息

Brain Res. 1995 Sep 4;690(2):231-5. doi: 10.1016/0006-8993(95)00559-9.

Abstract

The activity of NADPH-diaphorase (NADPH-d), a marker for nitric oxide synthase (NOS), was examined histochemically in the rat and mice retina. Mice in which the neuronal NOS gene has been disrupted (nNOS- mice) were used for specificity controls. Light microscopically a few amacrine cells were heavily stained. Other cells were stained weakly or not at all. Under the electron microscope, formazan precipitates were detectable on membranes of endoplasmic reticulum, nuclear envelope, mitochondria, and, in a few cases, the Golgi complex. Bipolar, horizontal, and Müller cells, were if at all, sparsely labeled with formazan. Labeled mitochondria were observed in rod endings and in inner segments of photoreceptors. Outer segments of photoreceptors and ganglion cells were completely free of reaction product. The NADPH-d reaction in wild-type mice displayed a similar distribution pattern to that in rats. Retinae of nNOS- mice showed a complete lack of prominent NADPH-d stained (amacrine) cells. None or a very few labeled membranes were seen.

摘要

采用组织化学方法检测了大鼠和小鼠视网膜中作为一氧化氮合酶(NOS)标志物的还原型辅酶Ⅱ黄递酶(NADPH-d)的活性。利用神经元型NOS基因被破坏的小鼠(nNOS-小鼠)进行特异性对照。光学显微镜下,少数无长突细胞被重度染色,其他细胞染色较弱或未被染色。在电子显微镜下,在内质网、核膜、线粒体膜上可检测到甲臜沉淀,少数情况下在高尔基体复合体上也可检测到。双极细胞、水平细胞和米勒细胞即使有标记,也只是被甲臜稀疏标记。在视杆末端和光感受器的内节观察到有标记的线粒体。光感受器的外节和神经节细胞完全没有反应产物。野生型小鼠中的NADPH-d反应显示出与大鼠相似的分布模式。nNOS-小鼠的视网膜显示完全缺乏显著的NADPH-d染色(无长突)细胞,未观察到或仅观察到极少数有标记的膜。

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