Capillary detection in transverse muscle sections

Author(s):  
Moi Hoon Yap ◽  
Ahmad Nadim Baharum ◽  
Glenn Ferris ◽  
Hans Degens ◽  
Ezak Fadzrin Ahmad Shaubari
Keyword(s):  
1964 ◽  
Vol s3-105 (71) ◽  
pp. 325-329
Author(s):  
M. P. OSBORNE

The anatomy and histology of the unpaired ventral nerves are described from light-and electron-microscopical studies. Seven unpaired nerves arise from the median dorsal surface of the ventral ganglionic nerve-mass, and terminate in abdominal segments 2 to 8 respectively. Each unpaired nerve bifurcates, sending a lateral nerve to both sides of its respective segment. Subsequently the lateral nerve gives rise to 2 nerve-branches. The first branch runs to a multipolar neurone that is associated with the tracheal system, and the second branch passes beneath the ventral longitudinal muscles and terminates on a ventral transverse muscle. Structurally, the unpaired nerve consists of axons ensheathed by Schwann-cells, the cytoplasmic processes of 2 giant Schwann-cells forming the entire neurilemma sheath of the nerve and its branches. A basement membrane, or connective-tissue sheath, about 2 µ thick surrounds the Schwann-cells. Four nerve-fibres are found in the unpaired nerve; 2 of these bifurcate, sending a fibre into both lateral nerves, but the other 2 fibres pass without dividing, into the left and right lateral nerves respectively, making a total of 3 fibres in both lateral nerves. One fibre from the lateral nerve enters the nerve-branch leading to the multipolar neurone associated with the tracheal system, and eventually joins its cell-body. This fibre is the axon of the neurone. The remaining 2 fibres in the lateral nerve pass into the nerve-branch that runs to the ventral transverse muscle. A comparison is made between the unpaired nerves of the blowfly larva and those in other insects.


1957 ◽  
Vol s3-98 (43) ◽  
pp. 315-326
Author(s):  
ARTHUR HESS ◽  
A. I. COHEN ◽  
ELAINE A. ROBSON

Sections of hydra studied with the electron microscope show various structures which have been identified by referring to control histological sections and to previous descriptions. Certain features have also been examined in frozen-dried sections under the light microscope. In the ectoderm, epithelio-muscular cells contain various organelles, and also smooth longitudinal muscle-fibres with which mitochondria may be associated. The so-called ‘supporting fibres’ appear to be thin bundles of muscle-fibres. Although points of contact exist between muscle-fibres, there appears to be no cytoplasmic continuity. The muscle-fibres insert on the mesogloea, and appear to be separated from it by two membranes, one belonging to the cytoplasm surrounding the musclefibreand the other to the mesogloea. The mesogloea is extracellular and quite distinct from the intracellular muscle-fibres. It appears granular and sometimes presents an indistinct fibrous background. In frozen-dried material the mesogloea stains blue with Mallory's method, while the muscle-fibres stain red. Two main types of cells are found in the endoderm. Among these, some of the digestive cells contain transverse muscle-fibres, but they are less distinct than the longitudinal ectodermal fibres. Otherwise the digestive cells vary much in structure, but generally they contain vacuoles and their free surface is thrown into villi covered with small granules. The ‘foamy gland cells’ are filled with much larger vacuoles containing granular material. The vacuoles are discharged together with portions of cytoplasm, and at this stage lamellated double membranes and mitochrondria appear between the vacuoles. Both types of cell possess two flagella, which show a typical ultrastructure and are surrounded by a thick membrane. Various other cells of the ectoderm are distinguished by their characteristic appearance. Cnidoblasts, for instance, have been found to contain an extensive system of intercommunicating vacuoles bounded by membranes, and do not resemble the interstitial cells. In unexploded penetrant nematocysts the tube is preformed and the butt nd stylets can also be seen. The special gland-cells of the pedal disk show large, lectron-dense granules which are extruded from the cell without any cytoplasm. A relatively thick homogeneous layer on the surface of the pedal disk is distinguished by the electron microscope.


2019 ◽  
Vol 45 (3) ◽  
pp. 672-683 ◽  
Author(s):  
Massimo Salvi ◽  
Cristina Caresio ◽  
Kristen M. Meiburger ◽  
Bruno De Santi ◽  
Filippo Molinari ◽  
...  

2017 ◽  
Vol 70 (4) ◽  
pp. 545-547
Author(s):  
Daichi Morioka ◽  
Nobuhiro Sato ◽  
Taro Kusano ◽  
Hideyuki Muramatsu ◽  
Shinya Yoshimoto

2017 ◽  
Author(s):  
Dan Puljan ◽  
Curt Anderson

It is well documented that coordination of feeding behavior in anuran amphibians requires precise coordination of the jaw levators and depressors with the timing of the protraction of the tongue. (for review, see Nishikawa, 2000). However, the neuronal mechanism initiating and synchronizing this coordination is not well understood. In addition to the intermandibularis muscle and tongue musculature in the lower jaw, there is a small, transverse muscle at the tip of the jaw, the m. submentalis. Previous anatomical work has demonstrated the presence of muscle spindles in the submentalis, leading to the hypothesis that the activation of this muscle may provide proprioceptive information to aid in coordinating the feeding biomechanics in Rhinella marina. Here, we demonstrate that the submentalis likely acts as a ‘trigger’ to initiate the hypoglossal nerve to activate the tongue, and without feedback information from the muscle spindles of the submentalis, tongue protraction is compromised.


2001 ◽  
Vol 44 (1) ◽  
pp. 95-107 ◽  
Author(s):  
Hironori Takemoto

Skilled movements of the tongue in speech articulation reflect complex formation of the tongue musculature, although its description in the anatomical literature is rather limited for developing a realistic computational model of the tongue. This study presents detailed descriptions of the muscular structure of the human tongue based on macroscopic and microscopic observations and provides threedimensional schemata of the tongue musculature. Histologic examination revealed that the tongue consists of five strata, stacked along the courses of the fibers of the genioglossus muscle in proximal-distal directions. This stratum structure exists in the entire tongue tissue, indicating that the lingual musculature can be divided into the inner and outer regions. The former consisted of the "stem" and "core," and the latter of the "cover" and "fringe." In gross dissection, the tongue was cut into wedge-like blocks along the course of the genioglossus muscle to examine muscle fiber arrangement. Using this approach, it was determined that serial repetitions of "structural units" composed the inner musculature of the tongue. Each unit consisted of a pair of thin muscle fiber laminae; one was composed of the genioglossus and vertical muscles, and the other of the transverse muscle. In the apex, the laminae lacked the fibers of the genioglossus. These findings have been incorporated in three-dimensional schemata of the tongue musculature.


2018 ◽  
Vol 66 ◽  
pp. 57-62 ◽  
Author(s):  
Tobias Siebert ◽  
Norman Stutzig ◽  
Christian Rode

1989 ◽  
Vol 37 (6) ◽  
pp. 705 ◽  
Author(s):  
JN Caira

Sixteen specimens of the tapeworm Spiniloculus mavensis were collected from the spiral valve of the brownbanded bambooshark in Australia. These specimens were examined with both light and scanning electron microscopy (SEM) and were compared with specimens of Acanthobothrium lineatum. The scolices of 50% of the specimens of S. mavensis were spined. The concept of a loculus is discussed; it was determined that each of the bothridia of S. mavensis possesses three loculi distinguished by two types of costae. The anterior costa is composed of radial muscle fibres similar to the costae in other onchobothriids such as A. lineatum; the posterior costa consists of transverse muscle fibres with little external representation and is therefore difficult to see with SEM. It is suggested that this construction accounts for the disagreement among previous authors with respect to the number of post-hook loculi. The specific description of S. mavensis is supplemented and the description of Spiniloculus is emended.


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