The bovine tubouterine junction: general innervation pattern and distribution of adrenergic, cholinergic, and peptidergic nerve fibers

1993 ◽  
Vol 274 (3) ◽  
pp. 493-501 ◽  
Author(s):  
Karl-Heinz Wrobel ◽  
Richard Kujat
Keyword(s):  
Nerve Fibers ◽  
Innervation Pattern ◽  
Tubouterine Junction

A Simple, Reliable and Inexpensive Silver Stain for Nerve Fibers in Bleached Skin

1988 ◽  
Vol 43 (7-8) ◽  
pp. 606-608 ◽  
Author(s):  
Bernd Fritzsch ◽  
Harold H. Zakon
Keyword(s):  
Silver Staining ◽  
Nerve Fibers ◽  
Sensory Cells ◽  
Innervation Pattern ◽  
Silver Stain

A procedure for silver staining is described which leads to the selective and reliable impregnation of nerve fibers in bleached skin of vertebrates and invertebrates. In combination with osmium, the protocol enhances the staining of secondary sensory cells of mechanosensory and electrosensory organs so that the innervation pattern of each organ and the number of sensory cells per organ can easily be evaluated. The technique can be also used for staining nerve fibers in whole embryos.

Innervation pattern of guinea pig pulmonary vasculature depends on vascular diameter

1997 ◽  
Vol 82 (2) ◽  
pp. 426-434 ◽  
Author(s):  
Rainer Haberberger ◽  
Michael Schemann ◽  
Holger Sann ◽  
Wolfgang Kummer
Keyword(s):  
Substance P ◽  
Guinea Pig ◽  
Vascular System ◽  
Nerve Fibers ◽  
Pulmonary Trunk ◽  
Pulmonary Vasculature ◽  
Innervation Pattern ◽  
Vascular Tree ◽  
Arterial Tree ◽  
Small Arteries

Haberberger, Rainer, Michael Schemann, Holger Sann, and Wolfgang Kummer. Innervation pattern of guinea pig pulmonary vasculature depends on vascular diameter. J. Appl. Physiol. 82(2): 426–434, 1997.—The pulmonary vasculature is supplied by various neurochemically distinct types of nerve fibers, including sensory substance P-containing and autonomic noradrenergic, nitrergic, and cholinergic axons. Pharmacological experiments have suggested that various segments of the pulmonary vascular tree respond differently to the respective neuromediators. We, therefore, aimed to determine histochemically and immunohistochemically for each of these neurochemically distinct perivascular axons their quantitative distribution along the vascular tree from the extrapulmonary trunks to the smallest intraparenchymal ramifications in control guinea pigs ( n = 5). Generally, arterial innervation was more developed than that of veins. Along the arterial tree, noradrenergic and substance P-containing axons were ubiquitous from the pulmonary trunk to smallest intraparenchymal vessels, whereas nitrergic axons were practically restricted to large (>700-μm) extrapulmonary arteries. Cholinergic axons were regularly present at arteries down to 100 μm in diameter and innervated two-thirds of small arteries (50–100 μm). The results demonstrate that the noradrenergic vasoconstrictor innervation extends throughout the pulmonary vascular system whereas the innervation pattern with various types of vasodilator fibers changes with vascular diameter, parallel to known pharmacological differences in cholinergic and nitrergic vasodilator effects.

Noradrenergic and Cholinergic Reinnervation of Islet Grafts in Diabetic Rats

1996 ◽  
Vol 5 (1) ◽  
pp. 21-30 ◽  
Author(s):  
Harmina Houwing ◽  
Roelie M. Van Asperen ◽  
Eddy A. Van Der Zee ◽  
Paul T.R. Van Suylichem ◽  
A. Beate Oestreicher ◽  
...  
Keyword(s):  
Tyrosine Hydroxylase ◽  
Pancreatic Islets ◽  
Choline Acetyltransferase ◽  
Neuron Specific Enolase ◽  
Diabetic Rats ◽  
Nerve Fibers ◽  
Physiological Data ◽  
Innervation Pattern ◽  
Kidney Capsule ◽  
Specific Proteins

Grafted islets become denervated due to the islet transplantation procedure. The aim of the present study was 1) to examine whether islet grafts in the liver, the spleen, and under the kidney capsule in rats become reinnervated following the transplantation and experimental procedures used in our laboratory, 2) whether there is any difference in reinnervation at these different sites, and 3) how these results relate to previous physiological experiments. Isogeneic isolated islets were transplanted into diabetic Albino Oxford rats, resulting in normoglycaemia. After at least 5 wk, graft-receiving organs were removed and several antibodies were employed to detect insulin, neuron-specific proteins, and cholinergic and noradrenergic nerve fibers. Islets in all three receiving organs contained viable insulin-positive B-cells. Neuron-specific enolase (NSE) as well as the growth-associated protein B-50 was observed at all sites. The cholinergic marker choline acetyltransferase (ChAT) was localized in islets grafts at all sites, but with the lowest density in the spleen. Staining for the noradrenergic markers tyrosine hydroxylase (TH) and dopamine-β-hydroxylase (DBH) was observed in islet grafts at all sites with the lowest density in grafts under the kidney capsule. All these neurochemical substances were most frequently observed in fibers associated with blood vessels, which may be the route along which nerves grow into the graft. It can be concluded that 1) islet grafts in the liver, in the spleen and under the kidney capsule become reinnervated; 2) the innervation pattern of the islet grafts differs only slightly from that in the control pancreatic islets; and 3) in combination with our previously physiological data, we can conclude that these nerve fibers are, at least partly, functionally active.

Some Biological Applications of High Voltage Electron Microscopy

1974 ◽  
Vol 32 ◽  
pp. 298-299
Author(s):  
Hans Ris
Keyword(s):  
High Voltage ◽  
Chromosome Structure ◽  
Nerve Fibers ◽  
Good Resolution ◽  
High Voltage Electron Microscopy ◽  
Voltage Electron ◽  
University Of Wisconsin ◽  
High Voltage Electron ◽  
One Year ◽  
The University

The High Voltage Electron Microscope Laboratory at the University of Wisconsin has been in operation a little over one year. I would like to give a progress report about our experience with this new technique. The achievement of good resolution with thick specimens has been mainly exploited so far. A cold stage which will allow us to look at frozen specimens and a hydration stage are now being installed in our microscope. This will soon make it possible to study undehydrated specimens, a particularly exciting application of the high voltage microscope.Some of the problems studied at the Madison facility are: Structure of kinetoplast and flagella in trypanosomes (J. Paulin, U. of Georgia); growth cones of nerve fibers (R. Hannah, U. of Georgia Medical School); spiny dendrites in cerebellum of mouse (Scott and Guillery, Anatomy, U. of Wis.); spindle of baker's yeast (Joan Peterson, Madison) spindle of Haemanthus (A. Bajer, U. of Oregon, Eugene) chromosome structure (Hans Ris, U. of Wisconsin, Madison). Dr. Paulin and Dr. Hanna are reporting their work separately at this meeting and I shall therefore not discuss it here.

Fine Structure of Planarian Neuroglial Cell

1976 ◽  
Vol 34 ◽  
pp. 188-189 ◽  
Author(s):  
Michio Morita ◽  
Jay Boyd Best
Keyword(s):  
Endoplasmic Reticulum ◽  
Ventral Nerve Cord ◽  
Osmium Tetroxide ◽  
Golgi Body ◽  
Nerve Fibers ◽  
Neuroglial Cell ◽  
Glutaraldehyde Solution ◽  
Deep Indentation ◽  
Cytoplasmic Processes ◽  
Longitudinal Nerve

The species of the planarian Dugesia dorotocephala was used as the experimental animal to study a neuroglial cell in the ventral nerve cord. Animals were fixed with 3% buffered glutaraldehyde solution and postfixed with 1% buffered osmium tetroxide.The neuroglial cell is multipolar, expanding into three or four cytoplasmic processes with many daughter branches. Some neuroglial processes are found to extend perpendicular to the longitudinal nerve fibers, whereas others are seen to be parallel to them. The nucleus of the neuroglial cell is irregular in shape and frequently has a deep indentation. Convex portions of the nucleus seem to be related to the areas from which cytoplasmic processes are extended. Granular endoplasmic reticulum (Fig. 4), Golgi body (Fig. 2), mitochondria (Figs. 1 and 2), microtubules (Fig. 4), and many glycogen granules are observable in the electron dense neuroglial cytoplasm. Neuroglial cells are also observed to contain various sizes of phagosomes and lipids (Fig. 2).

Interpreting HVEM of muscle-cell impulse networks

1992 ◽  
Vol 50 (1) ◽  
pp. 126-127
Author(s):  
Paul DeCosta ◽  
Kyugon Cho ◽  
Stephen Shemlon ◽  
Heesung Jun ◽  
Stanley M. Dunn
Keyword(s):  
Structural Analysis ◽  
Muscle Cell ◽  
Electron Micrographs ◽  
Relative Size ◽  
Automatic Classification ◽  
Nerve Fibers ◽  
Analysis Algorithm ◽  
Structural Networks

Introduction: The analysis and interpretation of electron micrographs of cells and tissues, often requires the accurate extraction of structural networks, which either provide immediate 2D or 3D information, or from which the desired information can be inferred. The images of these structures contain lines and/or curves whose orientation, lengths, and intersections characterize the overall network.Some examples exist of studies that have been done in the analysis of networks of natural structures. In, Sebok and Roemer determine the complexity of nerve structures in an EM formed slide. Here the number of nodes that exist in the image describes how dense nerve fibers are in a particular region of the skin. Hildith proposes a network structural analysis algorithm for the automatic classification of chromosome spreads (type, relative size and orientation).

The innervation of toad lymph hearts: An ultrastructural study

1992 ◽  
Vol 50 (1) ◽  
pp. 898-899
Author(s):  
A.M. Pucci ◽  
C. Fruschelli ◽  
A. Rebuffat ◽  
M. Guarna ◽  
C. Alessandrini ◽  
...  
Keyword(s):  
Ultrastructural Study ◽  
Neuromuscular Junctions ◽  
Nerve Fibers ◽  
Lack Of Information ◽  
Lymph Heart ◽  
Muscular Pump ◽  
Structure And Ultrastructure ◽  
Heart Wall

Amphibians have paired muscular pump organs, called “lymph heart”, which rhythmically pump back the lymph from the large subcutaneous lymph sacs into the veins. The structure and ultrastructure of these organs is well known but to date there is a lack of information about the innervation of lymph hearts. Therefore has been carried out an ultrastructural study in order to study the distribution of the nerve fibers, and the morphology of the neuromuscular junctions in the lymph heart wall.

Innervation of endoneurial microvessels in human sural nerve

1992 ◽  
Vol 50 (1) ◽  
pp. 920-921
Author(s):  
John L. Beggs ◽  
Peter C. Johnson ◽  
Astrid G. Olafsen ◽  
C. Jane Watkins
Keyword(s):  
Blood Flow ◽  
Blood Vessels ◽  
Blood Supply ◽  
Peripheral Nerves ◽  
Sural Nerve ◽  
Nerve Fibers ◽  
Arterial Supply ◽  
Autonomic Nerve ◽  
Vasa Nervorum ◽  
Endoneurial Blood Flow

The blood supply (vasa nervorum) to peripheral nerves is composed of an interconnected dual circulation. The endoneurium of nerve fascicles is maintained by the intrinsic circulation which is composed of microvessels primarily of capillary caliber. Transperineurial arterioles link the intrinsic circulation with the extrinsic arterial supply located in the epineurium. Blood flow in the vasa nervorum is neurogenically influenced (1,2). Although a recent hypothesis proposes that endoneurial blood flow is controlled by the action of autonomic nerve fibers associated with epineurial arterioles (2), our recent studies (3) show that in addition to epineurial arterioles other segments of the vasa nervorum are also innervated. In this study, we examine blood vessels of the endoneurium for possible innervation.

Computer-Assisted Analysis of Multi-Color Confocal Microscopic Datasets: Automated Light Microscopic Discrimination of Synaptic Relationships

1996 ◽  
Vol 54 ◽  
pp. 284-285
Author(s):  
M Wessendorf ◽  
A Beuning ◽  
D Cameron ◽  
J Williams ◽  
C Knox
Keyword(s):  
Nerve Fibers ◽  
Confocal Scanning Laser Microscopy ◽  
Computer Assisted ◽  
Nerve Terminals ◽  
Neuronal Somata ◽  
Scanning Laser Microscopy ◽  
Confocal Scanning ◽  
Entire Cell ◽  
Confocal Scanning Laser ◽  
Assisted Analysis

Multi-color confocal scanning-laser microscopy (CSLM) allows examination of the relationships between neuronal somata and the nerve fibers surrounding them at sub-micron resolution in x,y, and z. Given these properties, it should be possible to use multi-color CSLM to identify relationships that might be synapses and eliminate those that are clearly too distant to be synapses. In previous studies of this type, pairs of images (e.g., red and green images for tissue stained with rhodamine and fluorescein) have been merged and examined for nerve terminals that appose a stained cell (see, for instance, Mason et al.). The above method suffers from two disadvantages, though. First, although it is possible to recognize appositions in which the varicosity abuts the cell in the x or y axes, it is more difficult to recognize them if the apposition is oriented at all in the z-axis—e.g., if the varicosity lies above or below the neuron rather than next to it. Second, using this method to identify potential appositions over an entire cell is time-consuming and tedious.

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