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Found: 5 471
Page 192 of 548-
[Glia in the hypoglossal nucleus of the rat following axotomy (author's transl)].
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The columnar organization of the second synaptic region of the visual system of Musca domestica. L. I. Receptor terminals in the medulla.
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Neurotoxic effects of alkyl mercury compound on myelinating cultures of mouse cerebellum.
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Ultrastructural study of electrophysiologically identified neurones in the paraventricular nucleus of the rat.
The ultrastructural characterization of electrophysiologically identified neurones of the rat paraventricular hypothalamic nucleus was performed with extracellular labelling technique. The extracellularly recorded neurons are labelled with an electrophoretic deposit of alcian blue contained in the recording micropipette. The neurone thus labelled takes on a dark and shrunken appearance which enables its detection among neighbouring cells without, however, concealing its main morphological characteristics. 1) Spontaneously firing neurones, invaded by an antidromic action potential elicited by electrical stimulation of the neurohypophysis, were identified as magnocellular cells containing dense-cored vesicles of 200-250 nm in diameter. Dense-cored vesicles were not found in the antidromically activated neurones devoid of spontaneous activity. 2) Trans-synaptically activated neurones in the PVN or in its dorso-lateral edge were small cells devoid of dense secretory vesicles. 3) PV neurones in which neurohypophysial stimulation evoked no response, contained small, dense vesicles (100 nm in diameter) comparable with those found in parvocellular peptidergic neurones.
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Ultrastructural organization of actin filaments in neurosecretory axons of the rat.
The ultrastructural organization of actin filaments was studied in the neurohypophysial system of the rat after heavy meromyosin (HMM) labeling. This structural pattern is characterized by (1) a straight arrangement of the filaments parallel to the axonal axis in the proximal nondilated parts of axons, (2) a central location within axonal dilatations, and (3) a higher concentration within axonal endings where the filaments form a complex three-dimensional network. The relationships of the filaments to other axonal structures and organelles was further studied by use of electron microscopic stereoscopy. The actin filaments frequently appear anchored to the axolemma with either polar arrangements of the arrowhead decoration (i) at structurally undifferentiated sites, and (ii) more particularly within perivascular endings, at sites with electron-dense thickenings. In all axonal divisions actin filaments are also found to bind to filamentous material surrounding the microtubules and to various organelles. Within the terminal portions of the axons actin filaments exhibit close relationships to neurosecretory granules and to the numerous smooth microvesicles found in this region. Such preferential relationships are particularly observed both in axon ;terminals and in pituicytes, with coated vesicles frequently binding actin filaments. In water-deprived rats, the concentration of actin filaments is conspicuously increased along the axons and more clearly in the axonal swellings and endings, where they form a more complex and interconnected network. These data are discussed in the light of a possible involvement of contractile proteins in the mechanisms of axonal transport and terminal release of neurosecretory products.
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Synaptic relationships between a multipolar stellate cell and a pyramidal neuron in the rat visual cortex. A combined Golgi-electron microscope study.
Two synapsing and impregnated neurons in the rat visual cortex have been examined by a combined Golgi-electron microscope technique in which the Golgi precipitate is replaced by gold particles. One of the neurons is a stellate cell with smooth dendrites and a well impregnated axon, while the other is a layer III pyramidal neuron. Light microscopy showed some boutons from the axonal plexus of the stellate cell closely apposed to the soma and dendrites of the pyramid and it was predicted that synapses were present at these sites. An electron microscopic examination of serial thin sections, in which the profiles of the impregnated neurons are marked by their content of gold particles, showed most of these predicted synapses to exist. Indeed, axon terminals of the stellate cell formed five symmetric synapses with the cell body of the pyramid, one with the apical dendritic shaft and three with basal dendrites. Reasons are given for believing these synapses to be inhibitory. In addition, it was found that one of the axon terminals of the stellate cell synapsed with one of that cell's own dendrites. The significance of this finding is discussed.
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Effect of oestrogen on the pituitary gland of male Syrian hamsters. I. Electron microscope studies of pars intermedia.
The ultrastructure of the pars intermedia of normal and oestrogen-treated male Syrian hamsters is described. 3 types of cell were observed in normal gland, namely, 2 types of "light" cell and a "dark" cell. Light cells were regular in shape with round or oval nuclei and could be divided into type 1 and 2 by the size of their granules 200 to 250 nm in type 1 and 100 to 150 nm in type 2. Dark cells were fewer in number, irregular in outline with highly-indented chromatin-rich nuclei and occasional secretory granules in the Golgi area. Treatment for 6 weeks with diethylstibestrol (DES) 0.6 mg in 0.2 ml distilled water subcutaneously 3 times per week failed to induce recognisable change in the pars intermedia although after 12 weeks treatment cytoplasmic changes were observed. From that time until the experiment ended after 30 weeks of treatment progressive changes indicative of enhanced synthesis of hormone were present, greater cytoplasmic volume, hypertrophy of the Golgi apparatus, marked development of endoplasmic reticulum and ribosomes, increased numbers of secretory granules and the presence of granules within granules.
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Time- and dose-dependent influence of ouabain on the ultrastructure of optic neurones.
The cardiac glycoside ouabain was injected into the eye-bulb of the teleost fish, Carassius carassius. Three doses of ouabain were used: 10(-4) M, 10(-5) M, 10(-6) M. The final concentrations in the vitreous body of the eye were approximately 3-10(-5) M, 3-10-6 M and 3-10-7 M, respectively. After 8 hrs, 1, 2, 4, 6 and 8 days the ultrastructural alterations of retinal ganglion cells, the optic axons near the bulb and the terminal segments in the optic tectum were studied. The high doses of ouabain induced an early necrobiosis of the cell bodies in the retina followed by degeneration in the nerve. This is characterized as a protracted form of Wallerian degeneration. The significance of the inhibition of Na+ -K+-activated ATPase at the perikaryal level for both the integrity of axonal morphology and the axonal flow is discussed.
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Fine structure of the anterior neurohypophysis of the pond-loach, Misgurnus fossilis L., with reference to the neurosecretory innervation of intrinsic cells of the pars distalis.
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Axonal transport of proteins in the optic nerve and tract of the rabbit.