ArticleJournal of molecular histology2008
Neuronal nitric oxide synthase immunopositive neurons in cat claustrum--a light and electron microscopic study.
Article in Journal of molecular histology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Who cites it
6 citing papers in PubMed, 12 citations in OpenAlex.
- The claustrum of the sheep and its connections to the visual cortex.Journal of anatomy · 2021Article
- Electron microscopic study of Golgi-impregnated and gold-toned neurons and fibers in the claustrum of the cat.Journal of molecular histology · 2018Article
- Yu-Tao Loo and the development of neuropsychology in China.Protein & cell · 2017Article
- Synaptic organization of striate cortex projections in the tree shrew: A comparison of the claustrum and dorsal thalamus.The Journal of comparative neurology · 2017Article
- Topographical distribution and morphology of NADPH-diaphorase-stained neurons in the human claustrum.Frontiers in systems neuroscience · 2014Article
- Light and electron-microscopic study of leucine enkephalin immunoreactivity in the cat claustrum.Journal of molecular histology · 2012Article
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6 authors at 1 institution in 1 country.
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Abstract
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 immunoreactive (nNOS-ir) neurons and fibers in the dorsal claustrum (DC) of a cat. In this respect the aims of this study were: (1) to demonstrate nNOS-ir in the neurons and fibers of the DC; (2) to describe their light microscopic morphology and distribution; (3) to investigate and analyze the ultrastructure of the nNOS-ir neurons, fibers and synaptic terminals; (4) to verify whether the nNOS-ir neurons consist a specific subpopulation of claustral neurons; (5) to verify whether the nNOS-ir neurons have a specific pattern of organization throughout the DC. For demonstration of the nNOS-ir the Avidin-Biotin-Peroxidase Complex method was applied. Immunopositive for nNOS neurons and fibers were present in all parts of DC. On the light microscope level nNOS-ir neurons were different in shape and size. According to the latter they were divided into three groups-small (with diameter under 15 microm), medium-sized (with diameter from 16 to 20 microm) and large (with diameter over 21 microm). Some of nNOS-ir neurons were lightly-stained while others were darkly-stained. On the electron microscope level the immunoproduct was observed in neurons, dendrites and terminal boutons. Different types of nNOS-ir neurons differ according to their ultrastructural features. Three types of nNOS-ir synaptic boutons were found. As a conclusion we hope that the present study will contribute to a better understanding of the functioning of the DC in cat and that some of the data presented could be extrapolated to other mammals, including human.
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