Neuronal nitric oxide synthase immunopositive neurons in cat vestibular complex: a light and electron microscopic study

被引:0
作者
V. Papantchev
A. Paloff
D. Hinova-Palova
S. Hristov
D. Todorova
W. Ovtscharoff
机构
[1] Medical University,Department of Anatomy and Histology
[2] Medical University,Department of Forensic Medicine
[3] University of Sofia,Department of General, Experimental and Genetic Psychology
来源
Journal of Molecular Histology | 2006年 / 37卷
关键词
Cat; Vestibular complex; NOS; Light microscopy; Ultrastructure;
D O I
暂无
中图分类号
学科分类号
摘要
Nitric oxide is a unique neurotransmitter, which participates in many physiological and pathological processes in the organism. Nevertheless, there are little data about the neuronal nitric oxide synthase immunoreactivity (nNOS-ir) in the vestibular complex of a cat. In this respect, the aims of this study were to: (1) demonstrate nNOS-ir in the neurons and fibers, from all major and accessory vestibular nuclei; (2) describe their light microscopic morphology and distribution; (3) investigate and analyze the ultrastructure of the NOS I-immunopositive neurons, fibers, and synaptic boutons. For demonstration of the nNOS-ir, the peroxidase–antiperoxidase–diaminobenzidin method was applied. Immunopositive for nNOS neurons and fibers were present in all major and accessory vestibular nuclei. On the light microscope level, the immunopositive neurons were different in shape and size. According to the latter, they were divided into four groups—small (with diameter less than 15 μm), medium-sized (with diameter from 15 to 30 μm), large type I (with diameter from 30 to 40 μm), and large type II (with diameter greater than 40 μm). On the electron microscope level, the immunoproduct was observed in neurons, dendrites, and terminal boutons. According to the ultrastructural features, the neurons were divided into three groups—small (with diameter less than 15 μm), medium-sized (with diameter from 15 to 30 μm), and large (with diameter greater than 30 μm). At least two types of nNOS-ir synaptic boutons were easily distinguished. As a conclusion, we hope that this study will contribute to a better understanding of the functioning of the vestibular complex in cat and that some of the data presented could be extrapolated to other mammals, including human.
引用
收藏
页码:343 / 352
页数:9
相关论文
共 201 条
[1]  
Aoki C(1997)NMDA-R1 subunit of the cerebral cortex co-localizes with neuronal nitric oxide synthase at pre- and postsynaptic sites and in spines Brain Res 750 25-40
[2]  
Rhee J(1990)Apparent hydroxyl radical production by peroxynitrite: implications for endothelial injury from nitric oxide and superoxide Proc Natl Acad Sci USA 87 1620-1624
[3]  
Lubin M(2005)NO signaling in the CNS: from the physiological to the pathological Toxicology 208 193-205
[4]  
Dawson TM(1983)Afferent and efferent connections of the medial, inferior and lateral vestibular nuclei in the cat and monkey Brain Res 278 29-51
[5]  
Beckman JS(1990)Immunocytochemical features of the vestibular nuclei in the monkey and cat J Hirnforsch 31 585-599
[6]  
Beckman TW(1986)Parvalbumin in most gamma-aminobutyric acid-containing neurons of the cerebral cortex Science 231 995-997
[7]  
Chen J(1994)The complex role of nitric oxide in the pathophysiology of focal cerebral ischemia Brain Pathol 4 49-57
[8]  
Marshall PA(1991a)Nitric oxide mediates glutamate neurotoxicity in primary cortical cultures Proc Natl Acad Sci USA 15 6368-6371
[9]  
Freeman BA(1991b)Nitric oxide synthase and neuronal NADPH diaphorase are identical in brain and peripheral tissue Proc Natl Acad Sci USA 88 7797-7801
[10]  
Bishop A(1993)Mechanisms of nitric oxide-mediated neurotoxicity in primary brain cultures J Neurosci 13 2651-2661